Pseudo-messenger RNA: phantoms of the transcriptome
The mammalian transcriptome harbours shadowy entities that resist classification and analysis. In analogy with pseudogenes, we define pseudo-messenger RNA to be RNA molecules that resemble protein-coding mRNA, but cannot encode full-length proteins owing to disruptions of the reading frame. Using a...
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creator | Frith, Martin C Wilming, Laurens G Forrest, Alistair Kawaji, Hideya Tan, Sin Lam Wahlestedt, Claes Bajic, Vladimir B Kai, Chikatoshi Kawai, Jun Carninci, Piero Hayashizaki, Yoshihide Bailey, Timothy L Huminiecki, Lukasz |
description | The mammalian transcriptome harbours shadowy entities that resist classification and analysis. In analogy with pseudogenes, we define pseudo-messenger RNA to be RNA molecules that resemble protein-coding mRNA, but cannot encode full-length proteins owing to disruptions of the reading frame. Using a rigorous computational pipeline, which rules out sequencing errors, we identify 10,679 pseudo-messenger RNAs (approximately half of which are transposon-associated) among the 102,801 FANTOM3 mouse cDNAs: just over 10% of the FANTOM3 transcriptome. These comprise not only transcribed pseudogenes, but also disrupted splice variants of otherwise protein-coding genes. Some may encode truncated proteins, only a minority of which appear subject to nonsense-mediated decay. The presence of an excess of transcripts whose only disruptions are opal stop codons suggests that there are more selenoproteins than currently estimated. We also describe compensatory frameshifts, where a segment of the gene has changed frame but remains translatable. In summary, we survey a large class of non-standard but potentially functional transcripts that are likely to encode genetic information and effect biological processes in novel ways. Many of these transcripts do not correspond cleanly to any identifiable object in the genome, implying fundamental limits to the goal of annotating all functional elements at the genome sequence level. |
doi_str_mv | 10.1371/journal.pgen.0020023 |
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In analogy with pseudogenes, we define pseudo-messenger RNA to be RNA molecules that resemble protein-coding mRNA, but cannot encode full-length proteins owing to disruptions of the reading frame. Using a rigorous computational pipeline, which rules out sequencing errors, we identify 10,679 pseudo-messenger RNAs (approximately half of which are transposon-associated) among the 102,801 FANTOM3 mouse cDNAs: just over 10% of the FANTOM3 transcriptome. These comprise not only transcribed pseudogenes, but also disrupted splice variants of otherwise protein-coding genes. Some may encode truncated proteins, only a minority of which appear subject to nonsense-mediated decay. The presence of an excess of transcripts whose only disruptions are opal stop codons suggests that there are more selenoproteins than currently estimated. We also describe compensatory frameshifts, where a segment of the gene has changed frame but remains translatable. In summary, we survey a large class of non-standard but potentially functional transcripts that are likely to encode genetic information and effect biological processes in novel ways. Many of these transcripts do not correspond cleanly to any identifiable object in the genome, implying fundamental limits to the goal of annotating all functional elements at the genome sequence level.</description><identifier>ISSN: 1553-7404</identifier><identifier>ISSN: 1553-7390</identifier><identifier>EISSN: 1553-7404</identifier><identifier>DOI: 10.1371/journal.pgen.0020023</identifier><identifier>PMID: 16683022</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Animals ; Bioinformatics - Computational Biology ; Biotechnology ; DNA Transposable Elements ; Evolution ; Evolution, Molecular ; Genes ; Genetics ; Genetics/Gene Expression ; Genomics ; Homo (Human) ; Humans ; MEDICIN ; MEDICINE ; Messenger RNA ; Mice ; Mus (Mouse) ; Promoter Regions, Genetic ; Proteins ; Proteins - genetics ; Pseudogenes ; Reproducibility of Results ; Ribonucleic acid ; RNA ; RNA, Messenger - genetics ; Sequence Alignment ; Transcription, Genetic</subject><ispartof>PLoS genetics, 2006-04, Vol.2 (4), p.e23-e23</ispartof><rights>COPYRIGHT 2006 Public Library of Science</rights><rights>2006 Frith et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited: Frith MC, Wilming LG, Forrest A, Kawaji H, Tan SL, et al. (2006) Pseudo-Messenger RNA: Phantoms of the Transcriptome. PLoS Genet 2(4): e23. doi:10.1371/journal.pgen.0020023</rights><rights>2006 Frith et al. 2006</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c872t-cc29d192049b6d3cd9cd93dbcebdd9f2da00e7f21dba51f54b28c425ca4763a83</citedby><cites>FETCH-LOGICAL-c872t-cc29d192049b6d3cd9cd93dbcebdd9f2da00e7f21dba51f54b28c425ca4763a83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1449882/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1449882/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,550,723,776,780,860,881,2096,2915,23845,27901,27902,53766,53768,79342,79343</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16683022$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-155797$$DView record from Swedish Publication Index$$Hfree_for_read</backlink><backlink>$$Uhttp://kipublications.ki.se/Default.aspx?queryparsed=id:1949827$$DView record from Swedish Publication Index$$Hfree_for_read</backlink></links><search><creatorcontrib>Frith, Martin C</creatorcontrib><creatorcontrib>Wilming, Laurens G</creatorcontrib><creatorcontrib>Forrest, Alistair</creatorcontrib><creatorcontrib>Kawaji, Hideya</creatorcontrib><creatorcontrib>Tan, Sin Lam</creatorcontrib><creatorcontrib>Wahlestedt, Claes</creatorcontrib><creatorcontrib>Bajic, Vladimir B</creatorcontrib><creatorcontrib>Kai, Chikatoshi</creatorcontrib><creatorcontrib>Kawai, Jun</creatorcontrib><creatorcontrib>Carninci, Piero</creatorcontrib><creatorcontrib>Hayashizaki, Yoshihide</creatorcontrib><creatorcontrib>Bailey, Timothy L</creatorcontrib><creatorcontrib>Huminiecki, Lukasz</creatorcontrib><title>Pseudo-messenger RNA: phantoms of the transcriptome</title><title>PLoS genetics</title><addtitle>PLoS Genet</addtitle><description>The mammalian transcriptome harbours shadowy entities that resist classification and analysis. In analogy with pseudogenes, we define pseudo-messenger RNA to be RNA molecules that resemble protein-coding mRNA, but cannot encode full-length proteins owing to disruptions of the reading frame. Using a rigorous computational pipeline, which rules out sequencing errors, we identify 10,679 pseudo-messenger RNAs (approximately half of which are transposon-associated) among the 102,801 FANTOM3 mouse cDNAs: just over 10% of the FANTOM3 transcriptome. These comprise not only transcribed pseudogenes, but also disrupted splice variants of otherwise protein-coding genes. Some may encode truncated proteins, only a minority of which appear subject to nonsense-mediated decay. The presence of an excess of transcripts whose only disruptions are opal stop codons suggests that there are more selenoproteins than currently estimated. We also describe compensatory frameshifts, where a segment of the gene has changed frame but remains translatable. In summary, we survey a large class of non-standard but potentially functional transcripts that are likely to encode genetic information and effect biological processes in novel ways. Many of these transcripts do not correspond cleanly to any identifiable object in the genome, implying fundamental limits to the goal of annotating all functional elements at the genome sequence level.</description><subject>Animals</subject><subject>Bioinformatics - Computational Biology</subject><subject>Biotechnology</subject><subject>DNA Transposable Elements</subject><subject>Evolution</subject><subject>Evolution, Molecular</subject><subject>Genes</subject><subject>Genetics</subject><subject>Genetics/Gene Expression</subject><subject>Genomics</subject><subject>Homo (Human)</subject><subject>Humans</subject><subject>MEDICIN</subject><subject>MEDICINE</subject><subject>Messenger RNA</subject><subject>Mice</subject><subject>Mus (Mouse)</subject><subject>Promoter Regions, Genetic</subject><subject>Proteins</subject><subject>Proteins - genetics</subject><subject>Pseudogenes</subject><subject>Reproducibility of Results</subject><subject>Ribonucleic acid</subject><subject>RNA</subject><subject>RNA, Messenger - 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subjects | Animals Bioinformatics - Computational Biology Biotechnology DNA Transposable Elements Evolution Evolution, Molecular Genes Genetics Genetics/Gene Expression Genomics Homo (Human) Humans MEDICIN MEDICINE Messenger RNA Mice Mus (Mouse) Promoter Regions, Genetic Proteins Proteins - genetics Pseudogenes Reproducibility of Results Ribonucleic acid RNA RNA, Messenger - genetics Sequence Alignment Transcription, Genetic |
title | Pseudo-messenger RNA: phantoms of the transcriptome |
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