Literature DB >> 9278476

Making (anti)sense of non-coding sequence conservation.

D J Lipman1.   

Abstract

A substantial fraction of vertebrate mRNAs contain long conserved blocks in their untranslated regions as well as long blocks without silent changes in their protein coding regions. These conserved blocks are largely comprised of unique sequence within the genome, leaving us with an important puzzle regarding their function. A large body of experimental data shows that these regions are associated with regulation of mRNA stability. Combining this information with the rapidly accumulating data on endogenous antisense transcripts, we propose that the conserved sequences form long perfect duplexes with antisense transcripts. The formation of such duplexes may be essential for recognition by post-transcriptional regulatory systems. The conservation may then be explained by selection against the dominant negative effect of allelic divergence.

Mesh:

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Year:  1997        PMID: 9278476      PMCID: PMC146938          DOI: 10.1093/nar/25.18.3580

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN: 0305-1048            Impact factor:   16.971


  53 in total

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5.  The nonamer UUAUUUAUU is the key AU-rich sequence motif that mediates mRNA degradation.

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Journal:  Mol Cell Biol       Date:  1995-04       Impact factor: 4.272

6.  Transcriptional regulation of the rat vascular endothelial growth factor gene by hypoxia.

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7.  Use of a marked erythropoietin gene for investigation of its cis-acting elements.

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8.  Regulation of vascular smooth muscle cell insulin-like growth factor I receptors by phosphorothioate oligonucleotides. Effects on cell growth and evidence that sense targeting at the ATG site increases receptor expression.

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Review 9.  Fascination with 2-5A-dependent RNase: a unique enzyme that functions in interferon action.

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Journal:  J Interferon Res       Date:  1994-06

10.  Hoxa 11 structure, extensive antisense transcription, and function in male and female fertility.

Authors:  H M Hsieh-Li; D P Witte; M Weinstein; W Branford; H Li; K Small; S S Potter
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  25 in total

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2.  Over 20% of human transcripts might form sense-antisense pairs.

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3.  The small introns of antisense genes are better explained by selection for rapid transcription than by "genomic design".

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4.  Highly expressed genes are associated with inverse antisense transcription in mouse.

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Review 5.  The silence RNA keeps: cis mechanisms of RNA mediated epigenetic silencing in mammals.

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Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2006-01-29       Impact factor: 6.237

6.  Evolutionary patterns of non-coding RNAs.

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7.  The antisense transcriptomes of human cells.

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Review 8.  Effects of length and location on the cellular response to double-stranded RNA.

Authors:  Qiaoqiao Wang; Gordon G Carmichael
Journal:  Microbiol Mol Biol Rev       Date:  2004-09       Impact factor: 11.056

Review 9.  Antisense RNA: function and fate of duplex RNA in cells of higher eukaryotes.

Authors:  M Kumar; G G Carmichael
Journal:  Microbiol Mol Biol Rev       Date:  1998-12       Impact factor: 11.056

10.  A conserved gene structure and expression regulation of miR-433 and miR-127 in mammals.

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Journal:  PLoS One       Date:  2009-11-25       Impact factor: 3.240

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