Genes

agene

2007-11-02T23:46:00.000-04:00

Gray Matters
Adeistic
Eine Kleine Nattermusing
eMusings
eVolition
Galaria
Godborygmi
Godspell Follies
MetaThoughts
Mimble Wimble
Naturalism
Logodaedaly
palimpsest
Salient
Science of Evolution
Sechuam
Sintheist
Tabula Flexuosa
The Scarlet A
Weltschauung

alternative splicing

2006-12-30T23:19:00.000-05:00

Alternative splicing is a carefully regulated, variable adaptation of the routine RNA modification process of pre-mRNA splicing. Alternative splicing enables a single gene to give rise to multiple versions of a protein. In 1980, a gene called IgM provided the first recognized example of alternative splicing in cells—there were earlier examples in viruses. It has since been demonstrated that cells employ alternative splicing to increase protein diversity toward a variety of biological ends.

A cell typically splices a single transcript in multiple ways to generate an assortment of proteins. Alternatively spliced exons tend to lie between those segments of a gene that encode the functional units, or domains, of a protein (introns). An average mammalian gene possesses eight or nine exons—since most human genes undergoing some form of alternative splicing, virtually all of these exons are candidates for elaborate control.

Alternative splicing depends upon a splice site and nearby enhancer and repressor sequences—short segments of RNA that couple with regulatory proteins. It has been estimated that the splicing of a single exon may be promoted by at least three to seven enhancer sequences. As a result of alternate splicing, mutations that alter a splice site or a nearby regulatory sequence can have subtle effects by shifting the ratio of the resulting proteins without entirely eliminating any form.

Alternative splicing can allow one gene to generate different proteins in different tissues. Many highly specialized brain proteins arise from differential splicing of genes that are also expressed in other tissues. Cells can even modify splicing in response to changing conditions, and not only can alternative splicing tweak the structure of a single protein, but it may also be a means of regulating entire pathways. alternative splicing - click on fig 1 for animation : life cycle of an mRNA ~ click on Quicktime Q :

HHMI Feature Article on Alternative Splicing : Artist's conception of AS
Controlling the Synapse — 49 Proteins at a Time : The Alternative Splicing Website : Alternative Splicing DB (ASDB) : DNA-RNA-ProteinNational Center for Biotechnology Information

base excision repair

2006-12-29T23:56:00.000-05:00

Base excision repair describes one form of excision repair in which damaged bases or incorrect bases are excised and replaced by specific enzymes that differ between species. However, the biochemical processes involved in BER are equivalent across species, so bacterial DNA repair functions can operate in eukaryotic cells, and vice versa. Damage is typically the result of deamination, alkylation, hydroxylation, or attack by an oxygen radical, while the incorrect base can be uracil substituted for thymine. Oxidative DNA lesions induced by oxygen free radicals such as superoxide and hydroxyl radicals appear to be repaired predominantly by base excision repair mechanisms. Further, BER is the major DNA repair system involved in removal of various oxidative DNA lesions induced by ionizing radiation - these include abasic sites and modified DNA base and sugar residues.

First, the altered base is excised by a specific DNA glycosylase, which breaks the beta N-glycosidic bond and creates an AP, or abasic site. This site is identical to that generated by spontaneous depyrimidination or depurination. Six DNA glycosylases have been identified in humans – each excises an overlapping subset of either spontaneously formed (such as hypoxanthine), oxidized (such as 8-oxo-7,8-dihydroguanine), alkylated (such as 3-methyladenine), or mismatched (for example, T:G) bases.

Next, the terminal sugar-phosphate is removed by an AP endonuclease (Ape1), leaving a 3’-OH terminal and an abnormal 5'-abasic terminus. The resulting gap is refilled by the 5’-deoxyribose-phosphodiesterase action of a DNA polymerase I (DNA polymerase beta in mammals), then the strands are re-ligated by DNA Ligase I or a complex of XRCC1 and LigIII.

An alternative BER pathway corrects errors involving more than one nucleotide. The Fen1 protein excises the long-patch structure that is produced by DNA polymerase strand displacement. This "long-patch" repair process is divided into two subpathways: a PCNA-stimulated, Pol-beta-directed pathway and a PCNA-dependent, Pol-delta/epsilon -directed pathway.

link to table - human DNA repair genes : diagram>BER

cis versus trans-acting factors

2006-12-28T23:36:00.000-05:00

Most often, signal elements act only on the intramolecular nucleotide sequence to which they are attached, and they are said to act "in cis". Intron removal in eukaryotes involves cis-splicing. Interaction with signal factors -- usually protein molecules -- turns signal elements on or off.

When protein factors are free to diffuse within the cell they can act on target elements that may not be derived from the same genome segment. Protein factors capable of acting upon other intermolecular genome segments are called "trans-acting factors".

One form of trans-splicing is the 'spliced leader' type, which is primarily found in protozoans (e.g. trypanosomes) and in lower invertebrates such as nematodes. This results in the addition of a capped, noncoding, spliced leader sequence to the 5' end of mRNAs.

Another form of trans-splicing is the 'discontinuous group II intron' type that occurs in plant/algal chloroplasts and plant mitochondria. This results in the joining of two independently transcribed coding sequences. Both spliced-leader and discontinuous group II intron trans-splicing are mechanistically similar to conventional nuclear pre-mRNA cis-splicing. Trans-splicing also occurs in mammalian cells, just as cis-splicing occurs in trypanosomes. It has been suggested that both trans- and cis-splicing are ancient acquisitions of the eukaryotic cell. (Abstract)

capping

2006-12-28T23:27:00.000-05:00

Capping is a form of RNA processing in which the 5’ end of the nascent pre-mRNA is capped with a 7-methyl guanosine nucleotide, 7-methylguanylate. Capping occurs shortly after initiation of transcription.

The 5' cap is retained in mature mRNAs. Capping is required to protect the RNA transcript from degradation. It plays an important role in mRNA transport to the cytoplasm and in the initiation of protein synthesis (translation) . life cycle of an mRNA ~ click on Quicktime Q

NCBI Molecular Cell Biology
Post-transcriptional Processing of RNAs

codon

2006-12-28T23:21:00.000-05:00

DNA

2006-12-27T23:25:00.000-05:00

DNA is deoxyribonucleic acid, the template for genetic instructions. DNA undergoes replication into complementary strands of DNA for reproduction, and transcription into RNA for the production of proteins. The nucleotide bases, adenine, thymine, cytosine, and guanine are coupled inside the double helix, while the ribose backbone curves around the edge.

Above - nucleobases form complementary pairs through hydrogen bonding. Adenine and thymine are coupled (broken lines), and cytosine couples with guanine. Below left - stick model with hydrogen bonds as broken lines. (click to enlarge image)

More at:
http://www.dnaftb.org/dnaftb/
http://www.dnalc.org/home.html
http://www.pbs.org/wgbh/aso/tryit/dna/

DNA polymerases

2006-12-27T23:24:00.002-05:00

MOLECULAR BIOLOGY: ON DNA POLYMERASES: "Evolution has produced a number of different types of DNA polymerase, but they all have a similar overall three-dimensional shape that has been likened to a right hand, with palm, finger and thumb domains [1]. Polymerases of the A and B families, such as polymerase d, replicate the bulk of genomic DNA during the cell cycle and have been streamlined for processivity and accuracy. These enzymes fit the DNA substrate tightly into their active site, where the replicating base pair is enclosed by the finger domain [2-4]. The mobility of the finger domain underlies a so-called 'induced-fit' mechanism for checking the fidelity of replication: only when an incoming nucleotide forms a perfect Watson-Crick pair with the template base can the fingers close and induce an active conformation of the polymerase. If, nevertheless, an erroneous nucleotide happens to be incorporated, the polymerase responds with conformational distortions of its active center. These induce replication pausing and translocation of the primer terminus towards the intrinsic 'proofreading' exonuclease activity, which removes the mispairing base so that synthesis can resume [5]." O. Fleck and P. Schär (Current Biology 2004 14:R389)

5 Carver, T.E.Jr. , Hochstrasser, R.A., and Millar, D.P. (1994). Proofreading DNA: recognition of aberrant DNA termini by the Klenow fragment of DNA polymerase I. Proc. Natl. Acad. Sci. USA 91, 10670-10674

DNA damage by ROS

2006-12-27T23:24:00.001-05:00

Measurement of Oxidative DNA Damage and Repair in the Aging and Diseased Human Brain Using Liquid and Gas Chromatography/Mass Spectrometry with Isotope Dilution: "There is accumulating evidence that reactive oxygen species (ROS) play an important role in aging and neurodegenerative disease. Genomic DNA appears to be a particularly important target for ROS, since human patients and knockout mice lacking the capacity to repair certain types of [sic] oxidative DNA damage experience neurodegeneration and show evidence of premature aging."

DNA repair

2006-12-27T23:24:00.000-05:00

dNTP: "In eukaryotes, DNA damage elicits a multifaceted response that includes cell cycle arrest, transcriptional activation of DNA repair genes, and, in multicellular organisms, apoptosis."

Damage to DNA can be caused by mutations such as replication errors, incorporation of mismatched nucleotides (substitution errors -- transitions and transversions) DNA damage can also result from unintentional and intentional environmental stimuli such as oxygen radicals, hydroxyl radicals, ionizing or ultraviolet radiation, toxins, alkylating agents, and chemotherapy agents, particularly anti-cancer drugs.

Damaged bases can be corrected by simple in situ chemical reversal of the defect, but excision-repair processes predominate. These important DNA repair mechanisms take advantage of the fact that DNA is double-stranded and that complementary sequences should match on both strands. So, if damage is confined to one strand, the damage can be accurately repaired by excision and replacement with DNA synthesized with the undamaged complementary strand acting as template. All organisms, prokaryotic and eukaryotic, utilize at least three enzymatic excision-repair mechanisms: base excision repair, mismatch repair, and nucleotide excision repair.

MOLECULAR BIOLOGY: ON DNA-REPAIR ENZYMESThe DNA-repair enzymes have the capability of searching through vast tracts of DNA to uncover subtle structural anomalies. The human repair enzyme 8-oxoguanine glycosylase (hOGG1) efficiently removes 8-oxoguanine (oxoG), a damaged guanine (G) base containing an extra oxygen atom, while it ignores undamaged bases. The structure of hOGG1 bound to undamaged DNA, reveals a unique strategy that permits faithful removal of damaged bases which do 'fit' into the oxoG slot at the enzyme's active site, while normal G bases do not.

Anders Jahres medisinske priser: modified: "To date, at least six distinct pathways of DNA repair have been discovered, comprising nucleotide excision repair , base excision repair , mismatch repair , repair by recombination (homologous and nonhomologous end rejoining), damage tolerance pathways (polymerase bypass) and different damage reversal mechanisms, involving close to 200 genes in human cells. "

PLoS Biology: Three New Phases of Repairing DNA Damage in E. coli: "E. coli SOS response has been used to study DNA repair for decades, and a great deal is known about how the more than 30 genes involved in the response function. Two proteins figure prominently in this response. The LexA protein acts as a repressor and inhibits the expression of SOS genes under normal conditions; in the event of DNA damage, the protein RecA inactivates the LexA repressor by enhancing its autocleavage into two fragments, which initiates the SOS response. "

Discovery Of Why Some DNA Repair Fails: Significant For Huntington's Disease And Colon Cancer: "Dr. McMurray's group studied a specific mismatch repair protein Msh2-Msh3 and found a paradox: Instead of helping repair DNA damage, under certain conditions, Msh2-Msh3 was actually harming the cell. Msh2-Msh3 did this when it arrived at the wrong place at the wrong time and bound to a specific portion of DNA (CAG-hairpin). This accident of binding at the CAG-hairpin altered the biochemical activity of Msh2-Msh3. This change in biochemical activity, in turn, promoted DNA expansion -- rather than repair -- and changed the function of Msh2-Msh3 from friend of DNA to foe by allowing damaged DNA to go unrepaired. Without DNA repair, mutations accumulate that lead to disease."

MOLECULAR BIOLOGY: ON DNA-REPAIR ENZYMES: "hOGG1 makes extensive contacts with the orphaned cytosine base, which ensures that oxoG is removed only when in the appropriate base-pairing context. Although extensive biophysical and structural studies intimate that there are general features of damaged bases that signal their presence to repair enzymes, the steps involved in finding damaged bases in a sea of normal ones are still unclear. Most mechanisms invoke the enzyme sliding or hopping along the DNA duplex until a damaged site is detected. A particularly intriguing question is whether normal bases are also extruded from the helix during the search process."

targeted genetic repair

2006-12-27T23:23:00.000-05:00

Targeted genetic repair: an emerging approach to genetic therapy -- Sullenger 112 (3): 310 -- Journal of Clinical Investigation: "Targeted gene repair is a powerful yet controversial technique developed to direct base changes in chromosomal genes, while RNA repair is an emerging strategy to alter the coding content of messenger RNAs.

Genetic repair strategies may have significant therapeutic and safety advantages over traditional gene therapy approaches for the treatment of many genetic disorders. Firstly, because the mutant genetic instructions are directly repaired, the corrected RNAs and/or DNAs will be maintained in their native sequence context and be regulated by their endogenous regulatory machinery. Secondly, in the instance where the mutant gene encodes a deleterious or dominant-negative mutant protein, repair of the mutant should simultaneously engender the regulated production of the wild-type protein while eliminating or reducing expression of the deleterious gene product. Finally, genetic repair strategies attempt to repair defective instructions in a site-specific manner. Therefore, once adequately developed, these strategies will result in less random mutagenesis of the genome and lead to fewer mutagenic side effects than do methods that randomly insert genes into the genome. "

J. Clin. Invest. 112:310-311 (2003). doi:10.1172/JCI200319419. Perspective : Targeted genetic repair: an emerging approach to genetic therapy

Related Free Full Text articles:
Hacein-Bey-Abina, S. et al.2003. A serious adverse event after successful gene therapy for X-linked severe combined immunodeficiency. N. Engl. J. Med. 348:193-194.[Free Full Text]
Long, M.B., Jones, J.P. III, Sullenger, B.A., and Byun, J. 2003. Ribozyme-mediated revision of RNA and DNA. J. Clin. Invest. 112:312-318. doi:10.1172/JCI200319386.[Free Full Text]
Lan, N. et al.1998. Ribozyme-mediated repair of sickle ß-globin mRNAs in erythrocyte precursors. Science. 280:1593-1596.[Abstract/Free Full Text]
Watanabe, T., and Sullenger, B.A. 2000. Induction of wild-type p53 activity in human cancer cells by ribozymes that repair mutant p53 transcripts. Proc. Natl. Acad. Sci. U. S. A. 97:8490-8494.[Abstract/Free Full Text]
Rogers, C.S., Vanoye, C.G., Sullenger, B.A., and George, A.L. 2002. Functional repair of a mutant chloride channel using a trans-splicing ribozyme. J. Clin. Invest. 110:1783-1789. doi:10.1172/JCI200216481.[Abstract/Free Full Text]
Broitman, S., Amosova, O., Dolinnaya, N.G., and Fresco, J.R. 1999. Repairing the sickle cell mutation. I. Specific covalent binding of a photoreactive third strand to the mutated base pair. J. Biol. Chem. 274:21763-21768.[Abstract/Free Full Text]
Vasquez, K.M., Narayanan, L., and Glazer, P.M. 2000. Specific mutations induced by triplex-forming oligonucleotides in mice. Science. 290:530-533.[Abstract/Free Full Text]

double strand breaks

2006-12-27T23:13:00.000-05:00

MRC Radiation and Genome Stability Unit: "DNA double-strand breaks (DSBs) are potentially lethal, recombinogenic lesions which can result from exposure to DNA damaging agents such as ionising radiation or endogenous events such as collapsed replication forks. Failure to correctly repair a DSB can result in cell death or tumorigenesis. Indeed many cancer genes have been found to function in DSB metabolism. Eukaryotic cells mount a coordinated response to DSBs which includes cell cycle arrest, DNA repair and transcriptional stress responses. These responses are controlled by the DNA integrity checkpoint, DNA repair and stress-activated MAP kinase pathways, respectively. "

enhancer

2006-12-26T23:24:00.000-05:00

An enhancer is a short DNA sequence that increases the level of expression of another gene, that is, the enhancer up-regulates transcription of genes within the regulated gene-cluster. Specific trans-acting, transcription factors bind to the enhancer to bring about the increase in transcription rate -- recruiting the initiation complex proteins, or stabilizing the initiation complex.

Because of looping of the DNA strands, there may be a separation of several thousand base pairs between the enhancer and initiator gene (start site). However, the enhancer and its regulated gene are located on the same chromosome.

The enhancer segment may be situated upstream or downstream of the enhanced gene, and its orientation is not fixed – that is, the enhancer’s sequence may be reversed without altering its function. Enhancer segments may be excised and repositioned without interrupting their regulatory function. Enhancers may occur within introns. Enhancers cause the opposite effect to that of silencers which repress transcription.

epigenetics

2006-12-26T23:15:00.001-05:00

Defining epigenetic states through chromatin and RNA - Nature Genetics: "The term 'epigenetics' is used to describe heritable changes in genome function that occur without a change in DNA sequence. As such, epigenetics lies at the heart of the cellular memory crucial for development and provides an important avenue for sustained response to environmental stimuli."

exon

2006-12-26T23:04:00.000-05:00

Exons are “the sequences of the primary RNA transcript (or the DNA that encodes them) that exit the nucleus as part of a messenger RNA molecule. In the primary transcript neighbouring exons are separated by introns.”

In other words, exons are those sections of DNA within a gene that are not spliced out from the transcribed precursor mRNA and that are retained in the final messenger RNA (mRNA) molecule. For many genes, each exon contains part of the open reading frame (ORF) that codes for a specific portion of the complete protein. However, the term exon is often misused to refer only to coding sequences for the final protein. This is inaccurate since many noncoding exons are known in human genes (Entrez).

The term "exon" was coined by Walter Gilbert in 1978. Gilbert shared the 1980 Nobel Prize in Chemistry with Paul Berg and Frederick Sanger.
The Exon-Intron Database

gene

2006-12-24T23:47:00.000-05:00

The genes are those portions of the genome that code for the production of proteins. Typically protein coding segments are found in the open reading frames of introns, though alternative splicing and other epigenetic modifications account for much of the complexity of the genome.

gene regulation

2006-12-24T23:46:00.001-05:00

Gene regulation mechanisms in eukaryotes, which possess a nuclear membrane, differ from those in prokaryotes. Because prokaryotes lack a nuclear membrane, simultaneous translation of a gene may commence before transcription is complete.

In eukaryotes mechanisms for control of gene expression:

Most commonly affect the rate of transcription.
Some alter the rate of RNA processing within the nucleus.
Some affect the stability and degradation of RNA molecules (nonsense-mediated decay, nonstop decay).
Some control the efficiency of ribosomal translation into ribosomal polypeptides and proteins.
Some allow for alternative splicing, which generates different proteins from the same archival DNA template.
Epigenetic mechanisms modify mRNAs.

genome

2006-12-24T23:46:00.000-05:00

The term genome refers to the complete hereditary information of an organism (archival DNA or RNA for some viruses). The genome includes both the genes (coding-sequences, domains) and the non-coding sequences – both exons, which include open reading frames, and introns. Similarly, the term proteome refers to an organism’s collection of proteins.

The genome possesses:

Exonal segments of DNA whose sequence encodes the pre-mRNA, and ultimately polypeptide and protein sequences.
Intronal segments that are excised by pre-mRNA splicing before transport of mature mRNA through nuclear pores to the cytoplasm where ribosomal translation into ribosomal polypeptides and proteins occurs.
A start site for transcription, the initiator gene.
Promoters, both a basal or core promoter located within about 40 bp of the start site, and an upstream promoter, which may extend over as many as 200 bp farther upstream.
Enhancers.
Insulators.
Silencers.

helicases

2006-12-23T23:47:00.000-05:00

"Since the discovery of the 'DNA unwinding enzyme,' it has become clear that helicases participate in virtually all cellular processes involving nucleic acids. Helicases are found in all three kingdoms of life and are extremely numerous: 1-2 percent of eukaryotic genes are helicases. Several severe human genetic diseases have been linked to mutations in helicases. . . The most fundamental activity for all helicases is translocation, the ability to move along nucleic acids. Translocation is powered by ATP hydrolysis; hence helicases are motor proteins. Many helicases function as a part of large macromolecular complexes. An example is chromatin remodeling, which regulates gene expression by controlling the DNA access in chromatin. Helicases are the central ATP-powered engines that drive the translocation of the chromatin-remodeling complexes along the DNA. . . Ha's lab measures FRET (fluorescence resonance energy transfer) between various sites on the protein and on the DNA to build dynamic structural models of the protein-DNA complex during translocation. "

HHMI News: DNA Enzyme Shows Unexpected Acrobatic Flair: "Helicase Protein: A helicase protein moving rapidly on a highly flexible single-stranded DNA track. Repetitive movement on the DNA may keep it clear of potentially toxic proteins. Watch Animation at Helicase 8KB Flash Animation(requires Flash Player) "

heterochromatin

2006-12-23T23:46:00.001-05:00

MOLECULAR BIOLOGY: CHROMATIN DNA PACKAGING AND GENE SILENCING

Cytological studies have demonstrated that much of the repetitious DNA is packaged in a condensed form referred to as heterochromatin. This packaging in the nucleosome limits transcription by rendering DNA segments inaccessible.

The packaged mode of heterochromatin is epigenetically inherited, in that the packaging state is typically maintained after replication and mitosis, independent of the underlying DNA sequence. This property implies a that a biochemical mark exists together with cellular machinery that can recognize and maintain the mark locally.

The heterochromatin of all eukaryotes is characterized by histone hypoacetylation, and by methylation of histone H3 on lysine 9 in higher eukaryotes. Some single-celled eukaryotes such as Saccharomyces lack methylation of H3. Heterochromatin Protein 1 (HP1) binds H3 methylated at lysine 9 (H3-mK9). HP1 is a highly conserved protein that directly associated with pericentric heterochromatin.

A Unified Mode of Epigenetic Gene Silencing RNA Meets Polycomb Group Proteins A Unified Mode of Epigenetic Gene Silencing:
Article Abstract: "Recently, an essential role for RNA in the epigenetic silencing of genes packaged within heterochromatin in animals has been recognized. The RNA appears to be involved in targeting chromatin remodeling activity to specific loci and in later maintaining the repressed state of the gene. Epigenetic silencing of Hox cluster genes by the Polycomb group proteins also involves the formation of a stably inherited repressive chromatin structure. Recent studies of the C. elegans PcG gene sop-2 revealed an evolutionarily conserved property of PcG proteins in the binding of RNA, suggesting an important role for RNA in PcG-mediated Hox gene repression."

initiators

2006-12-22T23:33:00.000-05:00

insulator

2006-12-22T23:23:00.000-05:00

An insulator is a section of DNA (40 bp or more) that is located between the enhancer(s) and the promoter, or between the silencer(s) and the promoter of adjacent genes or clusters of adjacent genes.

intron

2006-12-22T23:22:00.000-05:00

Because the exon segments of archival DNA are transcribed into messenger RNAs and translated into proteins, the earlier view of genes held that introns were solely ‘junk DNA’ or DNA 'deserts' because they do not contain ORFs to code for proteins. However, it has recently been recognized that some exons code for micro RNAs and represent a source of epigenetic coding.

Some segments that were formerly designated introns contain information for protein, and others code for RNA products and are thus not "junk" DNA. Other introns posses translatable nucleotide sequences that, in the absence of splicing, can generate production of novel peptides (maturases) fused to the peptide encoded by the N-terminal exons. In fungi, these peptide maturases, appear to function in intron removal. Their encoding in introns results in homeostatic regulation of their production. Maturase genes are interspersed within other genes.

“Group II introns are a novel class of RNAs (ribozymes) best known for their self-splicing reaction. Under certain in vitro conditions, the introns can excise themselves from precursor mRNAs and ligate together their flanking exons, without the aid of protein. The splicing mechanism is essentially identical to splicing of nuclear pre-mRNA introns (pre-mRNA splicing), and this similarity has led to the widespread belief that group II introns were the ancestors of spliceosomal introns, which make up 25% of the human genome.

Some group II introns have a second remarkable property: they encode reverse transcriptase (RT) ORFs and are active mobile elements. Such mobile group II introns can insert into defined sites at high efficiencies (called retrohoming), or can invade unrelated sites at low frequencies (retrotransposition).”

Ribozyme-mediated revision of RNA and DNA -- Long et al. 112 (3): 312 -- Journal of Clinical Investigation: "Group I introns are ribozymes that carry out two transesterification reactions in order to excise themselves from a precursor transcript. "

mismatch repair

2006-12-18T23:36:00.000-05:00

Most mismatches are caused by replication errors. However, mismatches can also be produced by other mechanisms, such as deamination of 5-methyl cytosine to generate T improperly paired to G. Where the appropriate DNA-N-glycosylase is available, mismatches can also be repaired by base excision repair.

Mismatch repair has been studied most extensively in E. coli, where the proteins MutS, MutL, and MutH initiate the repair process. Newly synthesized strands are not immediately methylated in E.coli. First, MutS recognizes and binds to true mismatches and insertions/deletions of up to 4 nucleotides. Next, MutL binds to and stabilizes this complex of MutS/mismatched strand. The MutS-MutL complex then activates MutH, which locates a nearby methyl group and creates a nick in the newly synthesized strand opposite the methyl group. Excision is accomplished in E.coli by cooperation between the UvrD (Helicase II) protein, which unwinds from the nick toward the mismatch, and a single-strand specific exonuclease of appropriate polarity. Finally, resynthesis by Polymerase III and ligation by a DNA ligase repair the sequence and re-ligate the strands.

Unlike the un-methylated new strands in E.coli, strand-specificity in eukaryotes may be signalled by single-strand nicks. In nascent eukaryotic DNA strands, single-strand breaks occur between Okazaki fragments in the lagging strand and at the 3' end of the leading strand.

Eukaryotes lack homologues of MutH and uvrD, but do possess numerous homologues of MutS and MutL (MSHs 1-6, MLHs 1-3 and PMS 1 or 2). In E.coli, MutS and MutL function as monomers. The homologous eukaryotic proteins function as heterodimers. Human cells also possess two heterodimers of MutS homologues – MutSalpha (MSH2/MSH6), which recognizes single base mismatches and small loops, and MutSbeta (MSH2/MSH3), which recognizes small loops.

In eukaryotic cells, several standard replication proteins are needed for mismatch repair. The "clamp" protein, PCNA is a cofactor for most DNA polymerases and stabilizes the MutS and MutL heterodimers at mismatch sites on DNA. Three MutL homolog dimers are also known – in humans, MLH1/PMS2, MLH1/PMS1, and MLH1/MLH3. Further, just as exonucleases are thought to be important for mismatch repair in prokaryotes, at least two nucleases appear to contribute to mismatch repair in eukaryotic cells – exonuclease 1 and Flap Endonuclease (FEN-1 or DNase IV; Rad27 in S. cerevisiae). PCNA is also required during the later DNA synthesis step of mismatch repair. The DNA synthesis step also requires RPA (the eukaryotic single-stranded DNA-binding protein), Replication factor C (which loads PCNA onto DNA molecules at primer termini) and DNA polymerase delta.

Hereditary non-polyposis colon cancer (HNPCC) is a form of colon cancer frequently associated with defects in the genes encoding MSH2 (about 35% of identified gene-defect cases) and MLH1 (about 60% of identified gene-defect cases). HNPCC is characterized by early age of onset and autosomal dominant inheritance with high penetrance.

nonsense-mediated decay

2006-12-17T23:20:00.000-05:00

Defusing Dangerous Mutations: Scientists Discover A New Way By Which Cells Control Genetic Errors: Adapted: "Nonsense-Mediated Decay (NMD), is a process by which cells destroy potentially harmful molecules. Both healthy and damaged proteins begin as instructions in genes. Cells transcribe this information and create an mRNA molecule, a template that will be used to create proteins. RNAs usually contain extra bits of code that have to be cut out before they can be used. During this cut-and-paste operation, cells attach a group of molecules called the exon junction complex (EJC) to the RNA. An RNA made from a mutant gene usually has an EJC in the wrong position, which activates NMD and destroys the RNA before it can be used to make flawed proteins. There are at least two kinds of NMD: one requires UPF2 and the other does not.
The presence or absence of UPF2 changes the composition of the EJC, giving it different surfaces to which other molecules attach. This affects the way that another component, called UPF1, fits onto the machine. UPF1 is directly responsible for calling up the NMD machinery. The study shows that UPF1 can be mounted on both EJC types; the final effect is the same – to efficiently destroy faulty RNAs. "

nonstop decay

2006-12-17T23:19:00.000-05:00

Researchers Discover New Mechanism That Targets And Destroys Abnormal RNA:
Adapted: "Messenger RNA molecules are the genetic templates for proteins. In constructing proteins, the mRNA template is transcribed from DNA genes and transported to the ribosomes -- the cell's protein "factories" that are large complexes of protein and RNA. Given the importance of mRNA as an information-carrying molecule, the machinery that regulates mRNA levels and destroys faulty mRNA is critical in ensuring that errors in the genetic code are not passed on to proteins.

Nonstop decay is mRNA turnover mechanism that has none of the properties of nonsense-mediated decay (NMD), or of normal mRNA turnover in the cell. Nonstop decay shares none of the enzymes required for nonsense-mediated decay. A multi-enzyme complex called the exosome is important for nonstop decay, site of binding of a specific adapter protein called Ski7p occurs."

One percent of genes in both humans and yeast produce mRNAs containing specific sequences that would trigger degradation of the RNA by nonstop decay. Nonstop mRNA transcripts might be important in enabling production of shortened proteins that are needed at specific stages of development. At later stages of development, when these truncated proteins are no longer needed, their mRNA could easily be destroyed by nonstop decay."

The original news release can be found here.

nucleic acids

2006-12-17T23:10:00.000-05:00

A nucleic acid is a large biochemical macromolecule composed of chains of nucleotides coding genetic information. The most common nucleic acids are deoxyribonucleic acid ( DNA ) and ribonucleic acid ( RNA ). Nucleic acids are found in all living cells – karyotes and eukaryotes – and in viruses. Monomeric nucleic acids are called nucleotides – each consists of a nitrogenous heterocyclic base (either a purine or a pyrimidine), a five-ring pentose sugar, and a phosphate group.

nucleosome

2006-12-17T23:09:00.001-05:00

MOLECULAR BIOLOGY: CHROMATIN DNA PACKAGING AND GENE SILENCING
The nucleosome is the basic repeat element of chromatin, and consists of 147 base pairs (bp) of DNA wrapped 1.7 times around an octamer of histone proteins (two copies each of the core histones H2A, H2B, H3, and H4).

Nucleosomes are connected by about 20 to 60 bp of linker DNA to form the 10-nm "beads-on-a-string" array. This can be further compacted into a "30-nm" chromatin fiber.

Two classes of model for chromatin have been proposed: (a) the "one-start helix" in which nucleosomes, connected by bent linker DNA, are arranged linearly in a higher order helix; or (b) the "two-start helix" in which nucleosomes, connected by straight linker DNA, zigzag back and forth between two adjacent helical stacks.

To distinguish between these two competing models of higher order chromatin folding, Dorigo and co-workers employed a fully defined in vitro system to generate regular nucleosomal arrays. Analysis of the length of the nucleosome stacks, now connected only by internucleosomal cross-links, revealed a two-start rather than a one-start organization. This interpretation was corroborated by electron microscopy. Thus, local interactions between nucleosomes can drive self-organization into a higher order chromatin fiber. Adapted from: Adone Mohd-Sarip and C. Peter Verrijzer (Science 2004 306:1484)

1. B. Dorigo et al., Science 306, 1571 (2004)

nucleotide

2006-12-17T23:08:00.000-05:00

Single chain (monomeric) nucleic acids are called nucleotides -- each consists of a nitrogenous heterocyclic base (either a purine or a pyrimidine), a pentose sugar, and a phosphate group.

nucleotide excision repair

2006-12-17T23:07:00.000-05:00

A nucleotide with abnormal alterations in its chemical properties is termed an elementary damage site (EDS). UV light is a frequent cause of damage to segments of DNA. Nucleotide excision repair is a multi-enzyme excision repair pathway targetted at damaged segments of DNA. Similar mechanisms exist in both prokaryotes and eukaryotes, and the mechanism is highly conserved in eukaryotes. The recognition of DNA damage is less specific in nucleotide excision repair (NER) than in base excision repair (BER), which targets damaged bases. Thus NER repairs a wider range of damage types than BER, irrespective of chromatin structure or the gene expression profile of a particular cell.

NER operates by: (a) recognition of the damaged DNA; (b) excision of an oligonucleotide of 24–32 residues by dual incision of the damaged strand on each side of the lesion; and, as for BER (c) filling in of the resulting gap by DNA polymerase; and (d) ligation of the nick. There is evidence that at least some steps of NER require ATP-dependent chromatin remodeling activities.

NER can operate by two pathways. The first pathway, global genome repair (GGR), acts on DNA lesions across the genome and is transcription-independent. The second NER pathway, transcription coupled repair, is coupled to active transcription and is directed to the transcribed strand of active genes.

clickable diagram - nucleotide excision repair : diagram>nucleotide excision repair : diagram>transition coupled repair : more detail NER defective medical disorders : free full text review article :

nuclear speckles

2006-12-17T23:06:00.000-05:00

New Gene Regulation Mechanism Discovered: "Dr. David Spector noticed that under standard growth conditions, a particular population of messenger RNA molecules lingered in the nucleus indefinitely--in structures they call 'nuclear speckles'--and never reached the cytoplasm.

One of Spector's graduate students developed a method for purifying speckles. That allowed the researchers to identify not only the many different protein components of speckles, but also the messenger RNAs that are the basis of the new study, published in the October 21 issue of the journal Cell. The study--spearheaded by Cold Spring Harbor Laboratory postdoctoral fellow Dr. Kannanganattu Prasanth--identified the first such messenger RNA: one transcribed from a mouse gene called mCAT2 that encodes a cell surface receptor.

The scientists learned from the work of others that the mCAT2 receptor is involved in the production of nitric oxide, and that nitric oxide production is stimulated by various stress conditions including wound healing and viral infection. " That told us that when cells are stressed, maybe the atypical messenger RNA is released from the nucleus, exported to the cytoplasm, and translated into protein, thus circumventing the time-consuming process of producing new messenger RNA and providing a rapid response to viral infection or other stresses," says Spector. To test this idea, the researchers mimicked the effect of viral infection by treating cells with interferon.

Sure enough, they discovered that the atypical mCAT2 messenger RNA in the nucleus was rapidly cleaved in response to interferon treatment, and that the protein coding portion of the molecule was then quickly exported to the cytoplasm and translated into protein. diagram.

" This 'cut and run' mechanism is a completely new paradigm of gene regulation, so studying it will keep us busy for a while. But we already suspect that there is going to be a large family of genes regulated in this way," says Spector.""

open reading frame

2006-12-16T23:18:00.000-05:00

Because codons occur in nucleotide triplets, from any point within the genome there are six possible reading frames (three in each direction). Open reading frames (ORFs) are those sequences of DNA or RNA that code for translation at ribosomes into polypeptides or proteins. Within the genome, (ORFs) lie between codons for initiation (start-code sequence) and termination (stop-code sequence).

A DNA open reading frame starts with ATG—coding for Met—in most species, and ends with a stop codon (TAA, TAG, or TGA). In prokaryotes, ORFs are usually the longest sequence without a stop codon. In eukaryotes, long ORFs can continue over non-translatable intron gaps, so spliced mRNA must be employed to determine ORFs. Short ORFs can occur outside genes – within the intron, segments of DNA outside genes that were formerly considered ‘junk’ DNA.

oxoG repair

2006-12-16T23:04:00.001-05:00

MOLECULAR BIOLOGY: ON DNA-REPAIR ENZYMES
The agents that cause oxidative damage to DNA include oxygen radicals and ionizing radiation. Oxidation of a guanosine base to form oxoG produces a subtle structural transformation that results in deleterious mutations because DNA polymerases misread oxoG as a thymine (T) during genome replication prior to cell division. The human oxoG repair enzyme (hOGG1) catalyses the excision of oxoG in the first step of base excision repair.

Structural studies of the glycosylase enzymes involved in the repair process reveal common features of damaged-base recognition. These include enzyme-initiated DNA distortion that flips the damaged base out from the DNA double helix for recognition within a base-specific cavity of the enzyme. (OGG1)

oxidative stress and DNA damage

2006-12-16T23:04:00.000-05:00

Oxidative Stress/DNA Damage and DNA Repair: "Oxidative stress is produced in cells by oxygen-derived species resulting from cellular metabolism and from interaction with cells of exogenous sources such as carcinogenic compounds, redox-cycling drugs and ionizing radiations. DNA damage caused by oxygen-derived species including free radicals is the most frequent type encountered by aerobic cells. DNA damage caused by oxygen-derived species including free radicals is the most frequent type encountered by aerobic cells. When this type of damage occurs to DNA, it is called oxidative DNA damage and it can produce a multiplicity of modifications in DNA including base and sugar lesions, strand breaks, DNA-protein cross-links and base-free sites. "

MOLECULAR BIOLOGY: ON DNA-REPAIR ENZYMESThe agents that cause oxidative damage to DNA include oxygen radicals and ionizing radiation. Oxidation of a guanosine base to form oxoG produces a subtle structural transformation that results in deleterious mutations because DNA polymerases misread oxoG as a thymine (T) during genome replication prior to cell division. The human oxoG repair enzyme (hOGG1) catalyses the excision of oxoG in the first step of base excision repair. Structural studies of the glycosylase enzymes involved in the repair process reveal common features of damaged-base recognition. These include enzyme-initiated DNA distortion that flips the damaged base out from the DNA double helix for recognition within a base-specific cavity of the enzyme. (OGG1)

MOLECULAR BIOLOGY: ON DNA-REPAIR ENZYMES: "hOGG1 makes extensive contacts with the orphaned cytosine base, which ensures that oxoG is removed only when in the appropriate base-pairing context. Although extensive biophysical and structural studies intimate that there are general features of damaged bases that signal their presence to repair enzymes, the steps involved in finding damaged bases in a sea of normal ones are still unclear. Most mechanisms invoke the enzyme sliding or hopping along the DNA duplex until a damaged site is detected. A particularly intriguing question is whether normal bases are also extruded from the helix during the search process."

polyadenylation

2006-12-15T23:21:00.000-05:00

Polyadenylation is a form of RNA processing in which the 3’ end of the pre-mRNA is cleaved before a stretch of adenosines are added to the end of the molecule. Employment of alternative polyadenylation sites can result in the insertion or deletion of sequences that control the stability of the mRNA, and thus the level of protein expression. The polyA tail is also involved in initiation of translation.

MOLECULAR BIOLOGY: ON TRANSCRIPTION TERMINATION: "A defining feature of mRNAs is a tail composed of a long string of adenosine nucleotides -- the poly(A) tail. This is not encoded by the gene but is added following cleavage of the nascent RNA transcript. Molecular factors that recognize the cleavage site, and cut the RNA, bind to a regulatory region of the transcribing RNA polymerase II called the carboxy-terminal domain (CTD). This interaction is important for recruiting the factors to the nascent transcript. In turn, these factors must be off-loaded from the polymerase onto the RNA at their site of action for transcription to be terminated(4,5). In fact, recognition of the cleavage site has been believed to be the key step in termination -- but the new data(1-3) show that this isn't the whole story."

RNA processing

2006-12-15T23:20:00.000-05:00

Posttranscriptional RNA processing is an important feature of eukaryotic cells.

Pre-mRNA processing takes place in the nucleus. RNA processing events include capping of the 5’ end on the pre-mRNA, pre-mRNA splicing to remove intronic sequences, and polyadenylation of the 3’ end of the pre-mRNA.

Capping of the 5’ end of the nascent pre-mRNA is performed soon after initiation of transcription. Cleavage, pre-mRNA splicing, and polyadenylation usually follow termination of transcription of short primary transcripts with few introns. However, introns often are spliced out of the nascent RNA before transcription of the gene is complete for large genes with multiple introns. diagram - pre-mRNA processing : animation of RNA splicing : animation - life cycle of an mRNA : diagram - spliceosome assembly :

NCBI Molecular Cell Biology
Post-transcriptional Processing of RNAs

pre-mRNA

2006-12-15T23:16:00.000-05:00

Precursor messenger RNAs, or heteronuclear RNAs (hnRNAs) are products of gene transcription found in the cell's nucleus, which contain bases complementary to those of the template DNA strand, including both exons and introns.

Following pre-mRNA processing, which includes capping, pre-mRNA splicing, alternative splicing, and polyadenylation, the mature mRNA is transported through nuclear pores into the cytoplasm.

pre-mRNA splicing

2006-12-15T23:15:00.000-05:00

Because eukaryotic RNAs are transcribed from intron containing genes, the sequences encoded by the intronic DNA must be removed from the primary transcript prior to the RNAs becoming biologically active. The process of intron removal is called RNA splicing, or pre-mRNA splicing. The intron-exon junctions (splice sites) in the precursor mRNA (pre-mRNA) are recognized by trans-acting factors (prokaryote RNAs are mostly polycistronic). In pre-mRNA splicing the intronic sequences are excised and the exons are ligated to generate the spliced mRNA.

Group I introns occur in nuclear, mitochondrial and chloroplast rRNA genes, group II in mitochondrial and chloroplast mRNA genes. Many of the group I and group II introns are self-splicing in that no additional protein factors are necessary for the intron to be efficiently and accurately excised and the strands reattached.

Group I introns require an external guanosine nucleotide as a cofactor. The 3'-OH of the guanosine nucleotide acts as a nucleophile to attack the 5'-phosphate of the intron's 5' nucleotide. The 3' end of the 5' exon is termed the splice donor site. The 3'-OH at the 3' splice donor end of the 5' exon next attacks the splice acceptor site at the 5' nucleotide of the 3' exon, releasing the intron and covalently attaching the two exons together.

Pre-mRNA processing takes place in the nucleus of eukaryotes, whereas lack of a nuclear membrane in prokaryotes permits initiation of translation while transcription is not yet complete.

Pre-mRNA processing events include capping of the 5’ end on the pre-mRNA, pre-mRNA splicing to remove intronic sequences, and polyadenylation of the 3’ end of the pre-mRNA. animation of RNA splicing requires Flash Player plugin - Download plugin: clickable slide show - spliceosome intron removal :

More in NCBI Molecular Cell Biology on-line text.

proteome

2006-12-15T23:14:00.001-05:00

The term proteome refers to an organism’s collection of proteins. A cellular proteome is the collection of proteins found in the particular cell type under a particular set of environmental conditions. The complete proteome for an organism is the potential complete set of proteins, and equates to the sum of cellular proteomes under all possible conditions. The term, introduced in 1995, is analogous to the term genome for nucleic acids, though the proteins themselves are coded for by a portion of the genome.

promoters

2006-12-15T23:14:00.000-05:00

regulatory proteins

2006-12-13T23:47:00.001-05:00

Regulatory proteins bind to segments of DNA and bring about gene gene regulation.

replication

2006-12-13T23:47:00.000-05:00

Helicases are a critical part of the DNA replication process because they unwind double-stranded DNA to create single strands suitable for copying by the replication machinery. This and other helicase activity in the cell depends on the ability of the helicase's protein “engine” to crawl along the DNA strand. This locomotion is powered by ATP, the cell's ubiquitous energy source.

Helicase ProteinA helicase protein moving rapidly on a highly flexible single-stranded DNA track. Repetitive movement on the DNA may keep it clear of potentially toxic proteins. Watch Animation 8KB Flash Animation(requires Flash Player)

repressors

2006-12-13T23:46:00.000-05:00

ribosomal structure

2006-12-13T23:37:00.000-05:00

MOLECULAR BIOLOGY: ON RNA STRUCTURE
Elucidation of the crystal structures of the ribosome and its subunits have greatly increased the store of information about RNA structure. This information is moving toward an understanding of the principles of RNA folding and of the molecular interactions generating functional capabilities of the ribosome and other RNA systems. Almost all of the possible types of RNA tertiary interactions have been found in ribosomal RNA. One of these interactions is an abundant tertiary structural motif called the A-minor interaction. It has been observed that this participates in both aminoacyl-transfer RNA selection and in peptidyl transferase. It may also play an important role in the structural dynamics of the ribosome.

RNA polymerase

2006-12-13T23:17:00.001-05:00

In prokaryotic cells, all RNA classes are synthesized by a single polymerase. In eukaryotic cells there are 3 distinct classes of RNA polymerase, RNA polymerase (pol) I, II and III. Each polymerase is responsible for the synthesis of a different class of RNA.

RNA polymerase I (Pol I) is dedicated to synthesis of pre-rRNA. RNA polymerase II (Pol II) initiates transcription at DNA sequences corresponding to the 5 Cap of mRNAs and transcribes pre-mRNA. RNA polymerase III (Pol III) transcribes tRNA genes, 5S-rRNA genes, and genes encoding several other small RNAs.

In order to begin transcription, RNA polymerase requires a number of general transcription factors (called TFIIA, TFIIB, and so on). The general transcription factors have been highly conserved in evolution.

All RNA polymerases are dependent upon a DNA template from which to synthesize RNA by addition of complementary bases to an elongating backbone. In RNA, U is substituted for T. The transcribed RNA is complementary to the template strand of the DNA duplex, and is a replica of base-sequences in the non-template, coding strand. The non-template strand is called the coding strand because its sequences are identical to those of the mRNA (with U substituted for T).

p53 - A 3D animation showing the molecule p53 binds to DNA and initiates the transcription of mRNA : diagram - pre-mRNA processing : diagram - intron excision in mRNA precursors : life cycle of an mRNA ~ click on Quicktime Q : alternative splicing - click on fig 1 for animation :
NCBI Molecular Cell Biology - Transcription Initiation Complex : Bacterial Transcription Initiation (NCBI MCB) : SUMMARY transcription initiation (NCBI MCB)

RNA

2006-12-13T23:17:00.000-05:00

In general, a cell has more RNA than DNA, mostly incorporated in ribosomes with a relatively low rate of turnover. Only a small portion of human DNA has coding potential. Almost all RNA sequences in the cytoplasm, being derived from DNA coding sequences, have functional significance, whether transcribed in coding for proteins (mRNA), in performing translation (ribosomal RNA as ribozymes, and tRNA), or in epigenetic mechanisms. Substantial damage to RNA induces apoptosis (cell death), so RNA repair mechanisms are vital to cells.

RNA differs from DNA in its general composition -- ribose is the sugar moiety in the nucleotide backbone, and uracil serves as a base.

miRNA

2006-12-13T23:16:00.004-05:00

microRNAs are a large class of 21 to 24 nucleotide non-coding RNAs that have probable regulatory roles in animals and plants.

mRNA

2006-12-13T23:16:00.003-05:00

Messenger RNA, abbreviated mRNA, results from transcription of the base sequence of a segment of single strand archival DNA in the cell's nucleus.

In eukaryotic cells, mRNAs are transcribed as pre-mRNA and processed into mature mRNA in the nucleus, then transported through nuclear pore complexes to the cytoplasm. In some cases, mRNAs are transported to specific areas of the cytoplasm before being translated by ribosomes.

Complex macromolecular machines, such as spliceosomes and the cleavage/ polyadenylation apparatus, control each of these fundamental processes. These macromolecular assemblages comprise scores of proteins, and in many cases RNAs. The complexity of these control-assemblages ensures accuracy in locating promoters and splice sites in the long length of DNA and RNA sequences. Further, the macromolecular machines provide various avenues for regulating synthesis of a polypeptide chain.

Regulation of mRNA stability is central to the post-transcriptional modulation of gene expression. Stability of mRNA varies considerably between mRNAs and can be modulated by extracellular stimuli. Tight control of mRNA stability permits rapid changes mRNA levels, providing a mechanism for prompt termination of protein production. The rate of mRNA decay is determined by cis-acting sequences within the mRNA, which are recognized by trans-acting factors. The best-characterized cis-acting sequences responsible for mRNA decay in mammalian cells are the AU-rich elements, AREs present within the 3'-UTRs of short-lived mRNAs. These AREs are involved in deadenylation and subsequent degradation of mRNAs, and they have also been observed to stimulate 5'-decapping.

Dysregulation of mRNA stability has been associated with different chronic inflammatory diseases, -thalassemia, cancer, and Alzheimer's disease.

A number of ARE binding proteins (ARE-bps) have been identified, which interact with AU- and U-rich regions. These include the ELAV protein family members (most important HuR), the ARE/poly-(U)-binding/degradation factor 1 (AUF-1, also named hnRNP D), the heteronuclear ribonucleoprotein A1 (hnRNP A1), the KH-type splicing regulatory protein (KSRP), tristetraprolin (TTP), the T cell-restricted intracellular antigen (TIA)-1 and the TIA-related protein (TIAR). The KH-type splicing regulatory protein, KSRP has been described as being essential for exosome-mediated degradation of ARE-containing mRNAs.

Full Text Research Article on KSRP-mediated reduction of iNOS expression.

animation - life cycle of an mRNA : animation ~ alternative splicing : NCBI Molecular Cell Biology - Contents : Google mRNA : Classes of RNA Polymerases : Mechanism of RNA Polymerases : Processes of Transcription : Post-transcriptional Processing of RNAs : RNA Splicing : Clinical Significance of Alternative and Aberrant Splicing

tRNA

2006-12-13T23:16:00.000-05:00

Largest Computational Biology Simulation Mimics Life's Most Essential Nanomachine: "The simulations also reveal that the essential translating molecule, transfer RNA, must be flexible in two places for decoding to occur, furthering the growing belief that transfer RNA is a major player in the machine-like movement of the ribosome. The simulation also sets the stage for future biochemical research into decoding by identifying 20 universally conserved ribosomal bases important for accommodation, as well as a new structural gate, which may act as a control mechanism during transfer RNA selection." The original news release can be found here. : Voxel simulation image : Image 2 : Image 3 : Image 4 : Image 5 : High res movie : Low res movie : See an image of the Q machine at http://www.lanl.gov/asci/.

ribozymes in repair of RNA and DNA

2006-12-13T23:14:00.000-05:00

Ribozyme-mediated revision of RNA and DNA -- Long et al. 112 (3): 312 -- Journal of Clinical Investigation: "Several classes of catalytic RNAs, or ribozymes, have the capacity to revise genetic information. Group I and Group II ribozymes are derived from naturally occurring Group I and Group II introns, respectively. These introns are found in the genes of a variety of lower eukaryotes and prokaryotes. They differ fundamentally from spliceosomal introns since Group I and Group II introns self-splice from the precursor RNA independent of the spliceosome. The intron adopts the catalytic structure that is capable of cleaving RNA splice sites and ligating the flanking exons together. In addition to self-splicing from RNA precursors, some Group II introns are able to reverse-splice into DNA. The splicing activity of these introns can be harnessed as a molecular tool that may potentially revise any gene of interest."

BIO.COM: Biotechnology & Pharmaceutical News, Jobs, Software, Reports, Books, Events: "Hairpin ribozyme . . . minimal RNA enzyme was discovered by botanists in plants infected by tobacco ring spot virus and a number of other viruses. It is what is known as plant satellite RNA.Satellite RNAs are parasitic pieces of RNA that are not exactly viruses because they don't encode for proteins. Instead, they catalyze simple cut-and-paste reactions in order to replicate themselves, exacerbating or ameliorating diseases caused by plant viruses. A plant that has tobacco ring spot virus, for instance, will be more diseased if it also has this satellite RNA. "

rRNA

2006-12-13T23:09:00.000-05:00

silencer

2006-12-12T23:37:00.000-05:00

Silencers are control sections of DNA that, like enhancers, may be located thousands of base pairs away from the gene they regulate. However, when transcription factors bind to them, expression of the gene they regulate is repressed. This is the opposite effect to that of enhancers, which increase rate of transcription.

"One basic premise of chromatin regulation is that genes are silenced through compaction of chromatin, which reduces the accessibility of DNA. In contrast, gene expression may require the "opening up" of chromatin. The Polycomb group (PcG) of gene repressors and the trithorax group (trxG) of gene activators are two antagonistic classes of proteins that may act through modulation of chromatin structure. Together, these factors maintain the gene expression patterns of key developmental regulators and hence are crucial players in cellular differentiation, stem cell renewal, and cancer." in:
MOLECULAR BIOLOGY: CHROMATIN DNA PACKAGING AND GENE SILENCING

snRNA

2006-12-12T23:35:00.000-05:00

snoRNA

2006-12-12T23:34:00.000-05:00

Small nucleolar RNAs

splice sites

2006-12-12T23:18:00.001-05:00

spliceosome

2006-12-12T23:18:00.000-05:00

Almost all eukaryotic protein-coding genomes contain non-coding intervening sequences called introns. Spliceosomes are complex ribonuclear machines in eukaryotes that remove the non-coding introns from primary transcript, precursor mRNA (pre-mRNA or hnRNA). Alternatively, the term spliceome can be used to describe the complete set of all possible alternative splices in an organism, analogous to the genome or proteome.

Spliceosomes are variably composed of as many as 300 distinct proteins and five RNAs, making them among the most complex macromolecular machines known. review article abstract. Essential components of the spliceosome are the small RNA-protein complexes called small nuclear ribonucleoproteins (snRNPs, pronounced 'snurps'). These are U1, U2, U4, U5, and U6, so named because they are rich in uridine nucleotides. In addition to snRNPs, splicing requires many non-snRNP protein factors. The snRNPs participate in several RNA-RNA and RNA-protein interactions.

The spliceosome recognizes specific 5' and 3' sites on the pre-mRNA. The intronal area between these locations is excised, and the two exons are spliced (ligated). diagram - formation of a spliceosome : diagram - intron excision in mRNA precursors : diagram - pre-mRNA processing : animation ~ alternative splicing : animation of RNA splicing requires Flash Player plugin - Download plugin: clickable slide show - spliceosome intron removal : alternative splicing - click on fig 1 for animation : life cycle of an mRNA ~ click on Quicktime Q : clickable slide show - spliceosome intron removal :

Aberrant splicing creates mutant proteins, while alternative splicing generates diversity. Splice variants and epigenetic mechanisms account for the ability of about 25,000 human genes to code for about 100,000 human proteins. In addition to this variation, and that provided by recombination, each human gene possesses at least two isoforms – one from each parent. X Inactivation

SSOs

2006-12-12T23:12:00.000-05:00

Increased efficiency of oligonucleotide-mediated gene repair through slowing replication fork progression -- Wu et al. 102 (7): 2508 -- Proceedings of the National Academy of Sciences: "In mammalian cells, the precise mechanism of SSO-mediated chromosome alteration remains to be established, and there have been problems in obtaining reproducible targeting efficiencies. It has previously been suggested that the chromatin structure, which changes throughout the cell cycle, may be a key factor underlying these variations in efficiency. "

start site

2006-12-12T23:10:00.000-05:00

trans-splicing ribozymes and therapeutics

2006-12-11T23:15:00.000-05:00

Ribozyme-mediated revision of RNA and DNA -- Long et al. 112 (3): 312 -- Journal of Clinical Investigation: "The therapeutic revision of RNA by ribozymes is mechanistically different from that of DNA. To revise RNA sequences, a Group I intron from Tetrahymena thermophila has been adapted for trans-splicing. Trans-splicing ribozymes splice therapeutic RNA sequences onto a target transcript in a process called ribozyme-mediated RNA repair. Considerable progress has been made in the development of trans-splicing ribozymes for therapeutic applications such as treating sickle cell disease and cancer." This is one of the relatively recent targeted genetic repair techniques.

"The spliceosome has also been shown to trans-splice RNA transcripts. Spliceosomal-mediated RNA trans-splicing is also called called SMaRT."

translation

2006-12-11T23:13:00.000-05:00

transcription

2006-12-11T23:11:00.000-05:00

In transcription, an RNA polymerase enzyme (RNAp, or pol III in eukaryotes) directs generation of a complementary strand of mRNA from DNA. The mechanism of alternative splicing enables to production of different mature mRNA molecules, depending on what sequences are treated as introns and what remain as exons.

Transcription involves 3 phases: initiation, elongation, and termination.
1. RNA polymerase II initiates transcription at the first nucleotide of the first exon of a gene.
2. The 5 end of the nascent RNA is capped with 7-methylguanylate (capping).
3. Transcription by RNA polymerase II terminates at any one of multiple termination sites downstream from the poly(A) site, which is located at the 3 end of the final exon.
4. After the primary transcript is cleaved at the poly(A) site.
5. A string of adenine (A) residues is added (polyadenylation). The poly(A) tail contains ≈250 A residues in mammals, ≈150 in insects, and ≈100 in yeasts.

In more detail: RNA polymerase binds to the promoter region of one strand of DNA (5’ end), and the DNA double helix is un-zipped into single strands. First, RNA polymerase requires a number of general transcription factors (called TFIIA, TFIIB, etc.). The promoter contains a DNA sequence called the TATA box, which is located 25 nucleotides away from the site of initiation of transcription. The TATA box is recognized and bound by transcription factor TFIID, which then enables the adjacent binding of TFIIB. The rest of the general transcription factors plus the RNA polymerase assemble at the promoter. diagram - initiation of transcription.

The RNAp enzyme moves toward the 3’ end, connecting complementary bases into an elongating chain of RNA nucleotides. At termination, the transcribed mRNA molecule is released from the DNA strand. In prokaryotic cells – without a nuclear membrane – translation may begin prior to termination. In eukaryotic cells – with a nuclear membrane – the processed mRNA moves through the nuclear pores into the cytoplasm, where ribosomes on the rough endoplasmic reticulum translate the mRNA code into a peptide or a protein. Epigenetic, alternative splicing mechanisms can edit the mRNA prior to its translation into protein.

Capping of the 5’ end on the pre-mRNA with 7-methylguanylate occurs soon after initiation of transcription, and the 5 cap is retained in mature mRNAs.

Cleavage, pre-mRNA splicing, and polyadenylation usually follow termination of transcription of short primary transcripts with few introns. However, introns often are spliced out of the nascent RNA before transcription of the gene is complete for large genes with multiple introns.

It was believed that most genes in higher eukaryotes are regulated by controlling their transcription. However, it is increasingly recognized that epigenetic mechanisms (such as alternative splicing) are important in generating many proteins from a single gene, accounting for the Human Genome Project’s discovery that a mere 30,000 genes code for about 100,000 proteins.

animation - start of transcription : animation - life cycle of an mRNA : animation ~ alternative splicing

More at NCBI Molecular Cell Biology - Transcription Initiation Complex : SUMMARY transcription initiation (NCBI MCB) : Processes of Transcription : Wikipedia : Central Dogma :

termination of transcription

2006-12-11T23:10:00.000-05:00

MOLECULAR BIOLOGY: ON TRANSCRIPTION TERMINATION: "Transcription termination is important, not least because stopping too late will disrupt the regulation of other genes on the same chromosome; stopping prematurely, meanwhile, would produce truncated and therefore defective mRNAs. . . termination on most genes has been found to occur at various positions rather than at a single site. Moreover, a discrete signal in the DNA that might define the termination site could not be identified. . . Recent work(1-3) address this problem and provides evidence in favor of a striking alternative mechanism: that the transcribing RNA polymerase is "torpedoed". The mRNA is cut while it is still being synthesized, with the liberated region forming the mRNA. The remaining RNA trails out of the transcribing RNA polymerase, and is attacked by an exonuclease -- an enzyme that can degrade the RNA from its free end. This enzyme chases after the polymerase, chewing up the RNA strand as it goes. When it catches up with the polymerase, transcription is terminated."

topics

2006-12-01T12:00:00.000-05:00

TOPICS
alternative splicing / base excision repair / cis versus trans-acting factors / capping / codon /
DNA / DNA repair / DNA polymerases / DNA damage by ROS / targeted genetic repair /
double strand breaks / enhancer / epigenetics / exon / gene / gene regulation / genome / helicases / heterochromatin / initiators / insulator / intron / mismatch repair / nonsense-mediated decay / nonstop decay / nucleic acids / nucleosome / nucleotide / nucleotide excision repair / nuclear speckles / open reading frame / oxoG repair / oxidative stress and DNA damage / polyadenylation / RNA processing / pre-mRNA / pre-mRNA splicing / promoters /
proteome / regulatory proteins / replication / repressors / ribosomal structure / RNA /
RNA polymerase / miRNA / tRNA / mRNA / ribozymes in repair of RNA and DNA / rRNA /
silencer / snRNA / snoRNA / spliceosome / splice sites / SSOs / start site / trans-splicing ribozymes and therapeutics / translation / transcription / termination of transcription /
Research techniques / siRNA

Research techniques

2006-11-30T23:59:00.000-05:00

Computer Simulation of Ribosome at LANL
exogenous nucleobase rescue of abasic substitutions
siRNA
SMaRT Spliceosome-Mediated RNA Trans-splicing
E-MAP Technique Offers New View of Dynamic Biological Landscape

Computer Simulation of Ribosome at LANL

2006-11-28T23:21:00.000-05:00

Largest Computational Biology Simulation Mimics Life's Most Essential Nanomachine: "The ribosome is so fundamental to life that many portions of this molecular machine are identical in every organism ever genetically sequenced. In developing the project, the team identified a corridor inside the ribosome that the transfer RNA must pass through for the decoding to occur, and it appears to be constructed almost entirely of universal bases, implying that it is evolutionarily ancient."

exogenous nucleobase rescue of abasic substitutions

2006-11-26T23:04:00.000-05:00

BIO.COM: Biotechnology & Pharmaceutical News, Jobs, Software, Reports, Books, Events: A research technique called 'exogenous nucleobase rescue of abasic substitutions' provides a method by which researchers are able to delete particular nucleobases from the active site of an RNA enzyme without disrupting its structure, and subsequently to restore activity by providing nucleobases in solution.

Exogenous nucleobase rescue involves substitution of RNA nucleotides of interest with abasic residues. These maintain the continuity of the RNA chain but have a single hydrogen atom in place of a critical nucleobase. The researchers insert small molecules to rescue the activity lost because of the missing nucleobase.

siRNA

2006-11-12T23:36:00.000-05:00

siRNA Technology and Applications: "Small interfering RNA (siRNA) is a tool that is revolutionizing bioscience research. The increased use of siRNA in peer reviewed publications clearly demonstrates that it is an incredibly powerful means to specifically knock-down a gene's message, and subsequently the protein level of the targeted gene. In this manner, cellular-based assays can be conducted in the absence and presence of the targeted gene's protein.

The value of such an experiment has long been known as researchers the world over have employed genetic knock-out technologies, dominant negatives and chemical inhibitors of protein activities to perform such experiments. The use of siRNA is replacing all three of these methodologies."

SMaRT Spliceosome-Mediated RNA Trans-splicing

2006-11-12T23:28:00.000-05:00

American Society of Gene Therapy News Release: "Current gene transfer methods rely on the efficient transfer of cDNAs to effect phenotypic change. A study presented at the American Society of Gene Therapy Annual Meeting demonstrated a new approach to gene therapy. The researchers developed in vivo data supporting a novel method for genetic repair based on the correction of mutant pre-mRNA.

Christopher Walsh, MD, and Hengjun Chao, MD, at the University of North Carolina at Chapel Hill and Gary Mansfield, MD, and collaborators at Intronn Inc, Rockville, MD, made use of a natural mechanism that splices out introns and joins together the protein-coding exons. The normal process is called 'cis-splicing.' The researchers developed a new technology, called 'Spliceosome-mediated RNA trans-splicing (SMaRT),' to correct the hemophilia phenotype in Factor VIII knock out mice. A gene therapy vector is made by inserting their 'trans-splicing cassette' into a viral vector.

The researchers found that when they injected their vector into the hemophiliac mice, a significant increase in functional Factor VIII was found in the bloodstream of the mice. This factor allowed the mice to survive the bleeding trauma, which is lethal to untreated hemophilia mice. They demonstrated that the mutant FVIII RNA was repaired and that 'RNA repair' occurred via trans-splicing.This novel RNA repair method can provide a new approach in gene therapy for many genetic diseases, which are difficult to deal with by current gene transfer methods."

chromosomes

2006-06-22T00:22:00.000-04:00

Genetic archival material is condensed into chromosomes (Left - click to enlarge image).

A chromosome contains a long strand of deoxyribonucleic acid containing genes, regulatory sequences, and non-coding sequences of nucleotides, in association with proteins.

The full chromosomal complement of a cell comprises the genome, which is the complete hereditary information of an organism contained within macromolecules of archival DNA.

The multiple nuclear chromosomes of eukaryotes comprise long helical strands of DNA wrapped around structural proteins called histones – this composite material is termed chromatin (diagram). Each eukaryotic chromosome comprises one or two (sister) chromatids, each with a kinetochore for attachment to a microtubule of the spindle apparatus during cell division. Chromatids have a long (q) and a short (p) arm attached to the centromere. Sister chromatids attach to each other, or to the spindle apparatus, by means of special proteins and DNA base sequences in the kinetochore region.

Chromosomes (Gk. 'colored bodies') are most visible during metaphase (tem), and least condensed (dispersed) when participating in expression (tem, tem2) such as occurs in cells with large undifferentiated nuclei (colored tem cancer cell, fluorescence microscopy of cancer, stem cells, immature cell with oncogene (black dots) ).

Prokaryotes mostly possess one, sometimes two* chromosomes termed nucleoids (tem). Prokaryotes lack a membrane enclosed nucleus and their DNA is usually contained in circular structures located within the cytosol, but may be organized as linear strands that are typically attached to the plasma membrane. Plasmids are small circular, extrachromosomal genetic elements that can be transmitted from one bacterium to another through pili during conjugation. (more)

Chromatin (DNA plus histone protein) exists in two basic forms (tem):
1. Euchromatin, from which DNA is being actively transcribed (expressed) into RNA for ultimate translation into polypeptide and protein molecules.
2. Heterochromatin, which consists of either:
a. Facultative heterochromatin, which is sometimes expressed.
b. Constitutive heterochromatin, which is located around the centromere and usually contains repetitive sequences, and which is never expressed.*for example, Vibrio cholerae and Deinococcus radiodurans

MicroRNA may have fail-safe role in limb development

2005-12-02T14:21:00.000-05:00

University of Florida News - MicroRNA may have fail-safe role in limb development: "Researchers report linking a specific microRNA - miR 196 - to limb development, a finding that may be useful in understanding birth defects.

More specifically, researchers report linking a specific microRNA ? miR 196 ? to limb development, a finding that may be useful in understanding birth defects.

Until about five years ago, genetic researchers focused on DNA, which contains all the genetic instructions for the human body, and RNA, which translates DNA?s message into proteins ? the building blocks of cells, organs and all of the various systems of the body.

Unnoticed next to the main ingredients, microRNAs were considered to be ?junk? DNA, leftovers from millions of years of evolution. More recently, this genetic material is suspected to be part of an intricate mechanism that helps repress about one-third of our 25,000 genes. It has been linked to diabetes, hepatitis C, leukemia, lymphoma and breast cancer.

But only now have microRNAs been connected to actual growth processes.

Scientists do not know exactly what is happening, but they think miR 196 acts as a protective mechanism in the hindlimbs in the event normal gene transcription goes awry.

?A large body of evidence indicates this new class of regulators is not something to turn things off in the first place, but a fail-safe,? said Clifford Tabin, a professor of genetics at Harvard Medical School and senior author of the research."

Scientists Discover How Protein Crucial For Motion Is Synthesized At The Right Place In The Cell

2005-11-24T16:57:00.000-05:00

Scientists Discover How Protein Crucial For Motion Is Synthesized At The Right Place In The Cell: "A protein called ZBP1 binds to the messenger RNA and 'escorts' it out of the fibroblast nucleus and into the cytoplasm. On reaching the cell's periphery, the messenger RNA is translated into actin protein responsible for cell motility.
This new study reveals another key role for ZBP1: Not only does ZBP1 bind to actin messenger RNA and guide it to the cell's periphery, but it also helps regulate where in the cell the messenger RNA is translated into actin."

Lasers Improve Scientists' Understanding Of Complex Proteins

2005-11-23T21:29:00.000-05:00

Lasers Improve Scientists' Understanding Of Complex Proteins: "Using a system called fluorescence resonance energy transfer (FRET) on a single molecule, a researcher at the Lawrence Livermore National Laboratory?s Physical Biosciences Institute (PBI) in collaboration with UCLA scientists found that the procedure that regulates genes in a strand of DNA is a single process."

Icthyostega: Upper Devonian

2005-11-10T19:11:00.000-05:00

PALEONTOLOGY: ON THE ADAPTATIONS OF AN ANCIENT AMPHIBIAN: "One of the defining events in the history of life was the emergence of terrestrial vertebrates from early fish. The oldest known fossils that illustrate the transition to land are those of Ichthyostega from the Upper Devonian of East Greenland. This 360-million-year-old amphibian resembled fish in many features of its skeleton, but possessed pelvic (hip) and pectoral (shoulder) girdles and limbs capable of supporting the body and allowing movement on land."

Important DNA Repair Mechanism Linked To Premature Aging Yields

2005-11-10T18:31:00.000-05:00

Important DNA Repair Mechanism Linked To Premature Aging Yields: "The first step in TCR is the recognition that an RNAPII is stalled. Subsequently one of several things must happen. Most theoretical models have assumed that the stalled RNAPII has to be degraded and moved out of the way so the lesion can be repaired, after which transcription of the gene must start over with a new RNAPII.
Other possibilities are that the original RNAPII is somehow made to start up again, bypassing the lesion, or that the RNAPII is made to back up, digesting some of the messenger RNA it has already made, and have another go at transcription. In these cases, the likelihood of errors in the transcribed RNA and eventually in the resulting protein is increased.
What Cooper and her colleagues found, however, was a different, unexpected path. It appears that instead of being removed, the stalled RNAPII can be left in place and remodeled by the protein machinery of transcription-couple repair, so that repairs to the DNA can proceed without the loss of the messenger RNA that has already been formed."

E-MAP Technique Offers New View of Dynamic Biological Landscape

2005-11-03T18:45:00.000-05:00

HHMI News: Technique Offers New View of Dynamic Biological Landscape: "A new technique for analyzing the network of genetic interactions promises to change how researchers study the dynamic biological landscape of the cell. The technology, which is called epistatic mini array profiles (E-MAP), has already been used to assign new functions to known genes, to uncover the roles of previously uncharacterized proteins, and to define how biochemical pathways and proteins interact with one another."

Dynamics of DNA transcription

2005-11-02T18:23:00.000-05:00

Los Alamos National Laboratory (LANL): Scientists model the dynamics of DNA transcription: "Genomic sequences consist of only four distinct nucleotides: adenine (A), guanine (G), cytosine (C) and thymine (T). This sequence is strung together by a sugar-phosphate backbone, and stabilized by a complementary strand of DNA that protects each base in the sequence as a pair, wrapped inside the familiar double helix. Genes are the stretches of DNA that contain the blueprints for specific protein and range in length from a few hundred to several thousands of base pairs. Think of them as discrete, linear 'files' stored within the genome. The sequential reading of these files by a protein complex is known as transcription. The modeling technique is capable of predicting transcription initiation sites in DNA sequences and may predict the binding sites of important proteins in the transcriptional process."

RNA Editing in African Trypanosomes

2005-10-30T15:56:00.000-05:00

BioBio Faculty: "The central dogma of Molecular Biology states a linear flow of genetic information: DNA to/from RNA to protein. However, recently discovered processes of RNA editing which modify the genetic material during or after transcription expand this paradigm. A dramatic example is the post-transcriptional maturation of mitochondrial mRNAs by the addition and deletion of U residues in trypanosomes, whereby amino acid coding triplets and stop codons are created. Extensive editing in some mRNAs generates over half their mature size, yet a single error in the U-changes yields a frameshift. Trypanosome RNA editing is developmentally regulated and appears to control mitochondrial respiration.

In vitro studies have revealed that high fidelity RNA editing is directed by small transacting guide RNAs (gRNAs), and is catalyzed by a protein complex or editosome containing endonuclease, exonuclease, terminal transferase and RNA ligase. "

ribozyme group I intron

2005-10-30T15:39:00.000-05:00

Making sense of gene therapy: "He uses an RNA enzyme (ribozyme), called a Group I intron, to repair RNA. These introns cleave RNA at two sites, discarding the intervening RNA, before joining the ends back together.

Crucially, if the ribozyme has a sequence attached to its tail end, it sticks this into the RNA gap before gluing the whole thing back together; replacing one piece of RNA with another. In addition, the ribozyme recognizes its cleavage sites by base-pairing, so by changing the ribozyme sequence, it can be engineered to cut at different targets."

mRNA Cap Formation

2005-10-30T13:16:00.000-05:00

UB Department of Biological Sciences: Kiong Ho: "Cap formation is mediated by three enzymatic reactions in which the 5' triphosphate end of pre-mRNA is hydrolyzed to a 5' diphosphate by RNA triphosphatase, then capped with GMP by RNA guanylyltransferase, and methylated by RNA (guanine-N7) methyltransferase. The sequential steps in the capping reaction are universal to all eukaryotes, yet there is a significant divergence in the catalytic mechanism of the triphosphatase component. Metazoan triphosphatases belong to a superfamily of phosphatases that act via the formation and hydrolysis of a cysteinyl-phosphate intermediate. Fungal and viral triphosphatases comprise a novel family of metal-dependent phosphohydrolases with a unique tertiary structure."

mRNA Cap Formation in Parasitic Protozoa

2005-10-30T13:15:00.000-05:00

UB Department of Biological Sciences: Kiong Ho: "mRNA processing plays a critical role in the expression of eukaryotic genes. Processing occurs cotranscriptionally on nascent chains synthesized by RNA polymerase II. The earliest modification event is the addition of m7GpppN cap. This structural hallmark is present on all eukaryotic cellular mRNAs and is essential for viability. The cap enhances several downstream events in gene expression including mRNA stability, splicing of pre-mRNAs, and initiation of protein synthesis.

Structure of Mammalian RNA Triphosphatase

Structure of Fungal RNA Triphosphatase
Cap formation is mediated by three enzymatic reactions in which the 5' triphosphate end of pre-mRNA is hydrolyzed to a 5' diphosphate by RNA triphosphatase, then capped with GMP by RNA guanylyltransferase, and methylated by RNA (guanine-N7) methyltransferase. The sequential steps in the capping reaction are universal to all eukaryotes, yet there is a significant divergence in the catalytic mechanism of the triphosphatase component. Metazoan triphosphatases belong to a superfamily of phosphatases that act via the formation and hydrolysis of a cysteinyl-phosphate intermediate. Fungal and viral triphosphatases comprise a novel family of metal-dependent phosphohydrolases with a unique tertiary structure. "

RNA modulation, repair and remodeling by splice switching oligonucleotides

2005-10-30T13:11:00.000-05:00

"Targeting splicing by antisense oligonucleotides allows RNA modifications that
are not possible with RNA interference or other antisense techniques that destine
the RNA for destruction. By changing the ratio of naturally occurring splice variants
the expression of mRNA is modulated. By preventing the use of an aberrant splice
site created by a mutation and enforcing re-selection of correct splice sites the RNA
is repaired. Antisense induced skipping of the exon that carries a nonsense mutation
remodels the mRNA and restores the reading frame of the defective protein. All of
the above approaches have clinical applications. Modulation of splice variants is particularly
important since close to 60% of all genes code for alternatively spliced pre-mRNA."

Ryszard Kole, Tiffany Williams and Lisa Cohen
RNA modulation, repair and remodeling by splice switching oligonucleotides
Acta Biochimica Polonica Vol. 51 No. 2/2004

Ribozyme-mediated RNA repair

2005-10-30T13:01:00.000-05:00

Ribozyme-mediated revision of RNA and DNA -- Long et al. 112 (3): 312 -- Journal of Clinical Investigation: "The concept of ribozyme-mediated RNA repair was first demonstrated in Escherichia coli (2) and in cultured mammalian cells (7). "

DNA repair by AlkB

2005-10-29T23:52:00.000-04:00

ScienceWeek: "AlkB enzymatically demethylates the DNA bases adenine and
cytosine, unlike the suicidal Ada and Ogt proteins, by oxidative
demethylation: the methyl group is converted to an hydroxymethyl
group which then leaves the base as formaldehyde."

Rad51p Rad54p Rad52p

2005-10-29T14:42:00.000-04:00

Rad51p and Rad54p, but not Rad52p, elevate gene repair in Saccharomyces cerevisiae directed by modified single-stranded oligonucleotide vectors -- Liu et al. 30 (13): 2742 -- Nucleic Acids Research: "Synthetic single-stranded DNA vectors have been used to correct point and frameshift mutations in episomal or chromosomal targets in the yeast Saccharomyces cerevisiae. Certain parameters, such as the length of the vector and the genetic background of the organism, have a significant impact on the process of targeted gene repair, and point mutations are corrected at a higher frequency than frameshift mutations. Genetic analyses reveal that expression levels of the recombination/repair genes RAD51, RAD52 and RAD54 can affect the frequency of gene repair."

synthetic oligonucleotides

2005-10-29T14:39:00.000-04:00

In vivo gene repair of point and frameshift mutations directed by chimeric RNA/DNA oligonucleotides and modified single-stranded oligonucleotides -- Liu et al. 29 (20): 4238 -- Nucleic Acids Research: "Synthetic oligonucleotides have been used to direct base exchange and gene repair in a variety of organisms. Among the most promising vectors is chimeric oligonucleotide (CO), a double-stranded, RNA�DNA hybrid molecule folded into a double hairpin conformation: by using the cell�s DNA repair machinery, the CO directs nucleotide exchange as episomal and chromosomal DNA. Systematic dissection of the CO revealed that the region of contiguous DNA bases was the active component in the repair process, especially when the single-stranded ends were protected against nuclease attack."

DNA Size A Crucial Factor In Genetic Mutations, Study Finds

2005-10-28T14:59:00.000-04:00

DNA Size A Crucial Factor In Genetic Mutations, Study Finds: "The researchers investigated it by offering bases of different sizes to the DNA polymerase I enzyme and measuring how accurately the enzyme made new DNA copies. About once every 10,000 to 100,000 times the enzyme will put in the wrong base, choosing for instance a G instead of a T to pair with an A. The rate that the enzyme accurately copies DNA is known as its efficiency.
These rare and random mistakes can cause genetic mutations. While we tend to heap negative connotations onto the term, some mutations create new traits that actually benefit the organism or yield no effect. These small-scale changes, collectively called genetic drift, play an important role in evolution, as does natural selection. "

Transvection

2005-10-27T23:01:00.000-04:00

ScienceMatters @ Berkeley. Fly Guy: "In 1954, Nobel Laureate Ed Lewis, whom Levine calls the 'Einstein of flies,' proposed that a gene on one chromosome can directly affect the expression of its homologue gene on another chromosome, a process called transvection. However, the frequency of this 'crisscross' was unclear. Levine and Ronshaugen observed that, at least in the case of fruit flies, transvection is quite common.
'One possible explanation for transvection is maybe that it's used as a homeostasis mechanism,' Levine says. 'If an enhancer fails on one chromosome, the other chromosome can compensate. That way you make sure to get the right levels of expression.'"

Regulatory Genes & Enhancers

2005-10-27T22:59:00.000-04:00

ScienceMatters @ Berkeley. Fly Guy: "Regulatory DNA, Levine explains, controls how and where a gene is expressed in a cell. Of the three types of regulatory DNA--enhancer, silencer, and insulator--'enhancers are king, activating gene expression in specific cell types for specific tissues,' he says. Scientists conservatively estimate that while the human genome has less than 30,000 genes, it may contain 100,000 enhancers at the minimum. So far, just 50 or so have been identified."

Gene Regulation in Eukaryotes

2005-10-27T22:08:00.000-04:00

Gene Regulation in Eukaryotes: "Protein-coding genes have
exons whose sequence encodes the polypeptide;
introns that will be removed from the mRNA before it is translated [Discussion];
a transcription start site
a promoter
the basal or core promoter located within about 40 bp of the start site
an 'upstream' promoter, which may extend over as many as 200 bp farther upstream
enhancers
silencers"

genome.gov | Education Kit (Homepage)

2005-10-27T21:36:00.000-04:00

genome.gov Education Kit (Homepage): "Human Genome Project released a free, multimedia educational kit for high school students and the interested public. . . the contents of the education kit were reformatted and are available on this website in two formats; download modules or online viewing."

hapMap

2005-10-27T21:32:00.000-04:00

International Consortium Completes Map Of Human Genetic Variation: "In a paper in the Oct. 27 issue of the journal Nature, more than 200 researchers from Canada, China, Japan, Nigeria, the United Kingdom and the United States describe the initial results from their public-private effort to chart the patterns of genetic variation that are common in the world's population. The results provide overwhelming evidence that variation in the human genome is organized into local neighborhoods, called haplotypes, that usually are inherited as intact blocks of information.
At the project's outset in October 2002, the consortium set an ambitious goal of creating a human haplotype map, or HapMap, within three years. The Nature paper marks the attainment of that goal with its detailed description of the Phase I HapMap, consisting of more than 1 million markers of genetic variation, called single nucleotide polymorphisms (SNPs). The consortium is also nearing completion of the Phase II HapMap that will contain nearly three times more markers than the initial version and will enable researchers to focus their gene searches even more precisely on specific regions of the genome."

Epigenetics Alters How Our Genes Behave

2005-10-27T21:25:00.000-04:00

'Epigenetics' Means What We Eat, How We Live And Love, Alters How Our Genes Behave: "The fact that gene behavior is far more malleable than once believed has critically shifted the scientific community's course in mining the human genome, said Jirtle. No longer are mutant genes sought as the sole cause of disease. "

Scientists Unpick Genetics Of First 15 Minutes Of Life

2005-10-27T16:22:00.000-04:00

Scientists Unpick Genetics Of First 15 Minutes Of Life: "THIRA, ‘chaperones’ the early processes that take place once a sperm enters an egg, giving it a crucial role in the most fundamental process in sexually reproducing animals.

The absence or mutation of this gene in the maternal (mother’s) genome explains why eggs fail to produce a zygote – or early embryo - despite the presence of ‘healthy’ sperm.

The researchers looked at the genetic makeup of the sésame mutant and identified what is known as a point mutation in the HIRA gene -- showing that HIRA is the gene responsible for chaperoning the assembly of the sperm pro-nucleus."

Tsix transcription- versus RNA-based mechanisms in Xist repression and epigenetic choice.

2005-10-10T15:56:00.000-04:00

Entrez PubMed: "Recent inquiries have revealed a surprisingly large number (>2500) of naturally occurring antisense transcripts, but their function remains largely undiscovered. A better understanding of antisense mechanisms is clearly needed because of their potentially diverse roles in gene regulation and disease. A well-documented case occurs in X inactivation, the mechanism by which X-linked gene expression is equalized between XX females and XY males. The antisense gene Tsix determines X chromosome choice and represses the noncoding silencer, Xist. In principle, Tsix action may involve RNA, the act of transcription, or local chromatin. Here, we create novel Tsix alleles to distinguish transcription- versus RNA-based mechanisms. When Tsix transcription is terminated before Xist (TsixTRAP), Tsix cannot block Xist upregulation, suggesting the importance of overlapping antisense transcription. To separate the act of transcription from RNA, we knocked in Tsix cDNA in the reverse orientation (Tsix(cDNA)) to restore RNA levels in cis without concurrent transcription across Xist. However, Tsix(cDNA) cannot complement TsixTRAP. Surprisingly, both mutations disrupt choice, indicating that this epigenetic step requires transcription. We conclude that the processed antisense RNA does not act alone and that Tsix function specifically requires antiparallel transcription through Xist. A mechanism of transcription-based feedback regulation is proposed."

Shibata S, Lee JT.
Tsix transcription- versus RNA-based mechanisms in Xist repression and epigenetic choice.
Curr Biol. 2004 Oct 5;14(19):1747-54.

Fitting In: Newly Evolved Genes Adopt A Variety Of Strategies To Remain In The Gene Pool

2005-10-04T09:47:00.000-04:00

Fitting In: Newly Evolved Genes Adopt A Variety Of Strategies To Remain In The Gene Pool: "To determine the basis for the persistence of functional gene duplicates in the genome, three scientists at the Institute of Molecular Systems Biology at the Swiss Federal Institute of Technology in Zürich have collaborated on the largest systematic analysis of duplicated gene function to date. Using an integrative combination of computational and experimental approaches, they classified duplicate pairs of genes involved in yeast metabolism into four functional categories: (1) back-up, where a duplicate gene copy has acquired the ability to compensate in the absence of the other copy, (2) subfunctionalization, where a duplicate copy has evolved a completely new, non-overlapping function, (3) regulation, where the differential regulation of duplicates fine-tunes pathway usage, and (4) gene dosage, where the increased expression provided by the duplicate gene copy augments production of the corresponding protein.
Their results, which appear in the October issue of the journal Genome Research, indicate that no single role prevails but that all four of the mechanisms play a substantial role in maintaining duplicate genes in the genome."

Cold Spring Harbor Laboratory

Neuron: LEARNING AND MEMORY LTP makes dendrites excitable

2005-10-01T15:03:00.000-04:00

Since the pioneering work of Hebb, models to explain how memory traces are established have focused predominantly on plasticity at the synapse. However, it is becoming clear that changes in conductivity within the neuron are also important features of memory storage. It has already been shown that the induction of longterm potentiation (LTP) at a synapse can increase the intrinsic excitability of the postsynaptic neuron. Now, in Nature Neuroscience, Frick and colleagues propose a molecular mechanism to explain a link between LTP and dendritic excitability.

Frick et al. used a combination of calcium imaging and dendritic patchclamp recording to measure the activity of CA1 pyramidal neurons in slices of rat hippocampus. To gauge the excitability of individual dendrites, they measured the amplitude of action potentials that backpropagated from the soma into the dendritic tree. Before LTP was induced, the amplitude of the backpropagating action potential declined rapidly as it traveled towards the distal end of the dendrite.However, if LTP was induced at synapses within a dendrite, the propagation of the backpropagating action potential in that dendrite was enhanced. The attenuation of the backpropagating action potential that normally occurs along the dendrite has been attributed to a transient outward K+ current known as IA, which is mediated by A-type K+ channels. The authors asked whether the effect of LTP induction on backpropagating action potential amplitude was related to a change in IA, and they found that this current was indeed reduced around the potentiated synapses. The number of A-type K+ channels was unchanged, so Frick et al. concluded that LTP somehow brings about a change in the channel properties. What is the functional significance of this increase in dendritic excitability? Apart from the obvious effect of facilitating the transmission of information, it has been suggested that itbmight also prime the postsynaptic neuron to undergo subsequent plasticity — a phenomenon that is often referred to as metaplasticity. These findings illustrate that neuronal plasticity is a highly complex process that affects numerous aspects of neuronal activity, and the task of unravelling these complexities is set to keep researchers occupied for years to come.

Heather Wood
LEARNING AND MEMORY LTP makes dendrites excitable

References and links
ORIGINAL RESEARCH PAPER
Frick, A. et al.
LTP is accompanied by an enhanced local
excitability of pyramidal neuron dendrites.
Nature Neurosci. 7, 126–135 (2004)

FURTHER READING Stuart, G. et al.
Action potential initiation and backpropagation in neurons
of the mammalian CNS.
Trends Neurosci. 20, 125–131 (1997) |
Häusser, M. Storing memories in dendritic channels.
Nature Neurosci. 7, 98–100 (2004)
WEB SITES
Encyclopedia of Life Sciences:
http://www.els.net/
Long-term potentiation

Novel Mechanism For DNA Replication Discovered

2005-09-30T16:30:00.000-04:00

Novel Mechanism For DNA Replication Discovered: "Since the discovery of the structure of DNA by James Watson and Francis Crick in 1953, the paradigm for DNA replication has stated that the DNA itself codes for the appropriate pairings for replication. In other words, if a guanine base is on the original strand of DNA then its partner, a cytosine base, will pair to it on the replicated strand. In a study published in this week's issue of Science, researchers from Mount Sinai School of Medicine report on the first instance in which a protein, rather than the DNA, provides the coding information.

The study offers a specific mechanism by which cells cope with some of the most destructive carcinogens in the environment, including those in cigarette smoke. Many of these carcinogens preferentially damage DNA at guanine -- one of the four bases in DNA -- blocking, in some cases, the ability of the guanine to partner with cytosine, which can lead to mistakes during replication.

Aneel Aggarwal, PhD, and Deepak Nair, PhD, of the Department of Physiology and Biophysics at Mount Sinai School of Medicine and their colleagues at University of Texas Medical Branch, Galveston discovered that a protein called Rev1 DNA polymerase itself codes for a cytosine to be placed on the replicating strand. The cytosine is inserted based upon the coding information in Rev1 regardless of whether a guanine or another base is present on the DNA.

"This is the first time we have seen a protein serving as a template for DNA synthesis," said Dr. Aggarwal. "This provides an entirely new mechanism by which cells can replicate through DNA damaged by certain carcinogens. It thus opens a novel area of study with the potential for innovative approaches to prevention and treatment of cancer.""

The Mount Sinai Hospital / Mount Sinai School of Medicine

Synaptic Plasticity: BIOCHEMICAL MECHANISMS FOR TRANSLATIONAL REGULATION IN SYNAPTIC PLASTICITY

2005-09-28T18:14:00.000-04:00

Nature Reviews Neuroscience - Reviews: "Changes in gene expression are required for long-lasting synaptic plasticity and long-term memory in both invertebrates and vertebrates. Regulation of local protein synthesis allows synapses to control synaptic strength independently of messenger RNA synthesis in the cell body. Recent reports indicate that several biochemical signalling cascades couple neurotransmitter and neurotrophin receptors to translational regulatory factors in protein synthesis-dependent forms of synaptic plasticity and memory. In this review, we highlight these translational regulatory mechanisms and the signalling pathways that govern the expression of synaptic plasticity in response to specific types of neuronal stimulation.

Translation factors and translational control mechanisms are downstream targets of several signalling pathways and are crucial in synaptic plasticity. Some forms of translational control alter general protein synthesis, whereas others regulate translation of specific messenger RNAs (mRNAs).
Translation initiation refers to the assembly of a translation-competent ribosome at the AUG start codon on an mRNA. The first step involves the binding of the translation-initiation factor eIF2, which is a G protein, to methionyl-transfer RNA in a GTP-dependent manner.eIF2 has three subunits (, and ), and the conversion of inactive eIF2GDP to active eIF2GTP by eIF2B is blocked by phosphorylation of eIF2. Four kinases that are present in the brain — PKR, HRI, PERK and GCN2 — phosphorylate eIF2 on Ser51.
The eIF2B enzyme complex consists of five polypeptides (–), with eIF2B catalysing guanine nucleotide exchange on eIF2. The importance of eIF2B function in the brain is highlighted by the fact that mutations in each eIF2B subunit can cause leukoencephalopathy with vanishing white matter.
The integrity of the eIF4F cap-binding complex and, therefore, translation efficiency, is regulated by 4E-BPs. Phosphorylation of 4E-BPs by the extracellular signal-regulated kinase (ERK), phosphoinositide 3-kinase (PI3K) and mammalian target of rapamycin (mTOR) signalling pathways is crucial for protein synthesis-dependent synaptic plasticity and memory.
The cap-binding protein eIF4E is phosphorylated by the protein kinases Mnk1 and Mnk2, which are phosphorylated and activated by ERK and p38. eIF4E phosphorylation is associated with synaptic plasticity and memory.
In addition to regulating 4E-BP phosphorylation and function, mTOR directly phosphorylates and activates the S6 kinase (S6K), which phosphorylates the ribosomal protein S6, an essential component of the small, 40S ribosomal subunit. S6K and S6 phosphorylation have been implicated in synaptic plasticity and memory.
The cytoplasmic polyadenylation element (CPE) in the 3'-untranslated region is important in extension of the poly(A) tail and translation activation. Recent evidence indicates a crucial role for CPE-binding protein in long-term facilitation in Aplysia californica and in hippocampal synaptic plasticity."

Eric Klann & Thomas E. Dever
BIOCHEMICAL MECHANISMS FOR TRANSLATIONAL REGULATION IN SYNAPTIC PLASTICITY
Nature Reviews Neuroscience 5, 931-942 (2004); doi:10.1038/nrn1557

2004-10-24T11:58:00.000-04:00

internal links

2004-10-10T17:28:00.000-04:00