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...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:PLoS genetics 2006-04, Vol.2 (4), p.e23-e23
Hauptverfasser: 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
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page e23
container_issue 4
container_start_page e23
container_title PLoS genetics
container_volume 2
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
format Article
fullrecord <record><control><sourceid>gale_plos_</sourceid><recordid>TN_cdi_plos_journals_1313482863</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A146972402</galeid><doaj_id>oai_doaj_org_article_73e747585289450d9fbf58e975525f82</doaj_id><sourcerecordid>A146972402</sourcerecordid><originalsourceid>FETCH-LOGICAL-c872t-cc29d192049b6d3cd9cd93dbcebdd9f2da00e7f21dba51f54b28c425ca4763a83</originalsourceid><addsrcrecordid>eNqVk22L1DAQx4so3nn6DUQXhAPBrnlsknshLOfTwnEnp97bkCbT3Z5tU5vWh29vdrfqVhSVBDJMfvPPZIZJkvsYzTEV-Om1H7rGVPN2Bc0cIRI3vZEcYs5pKhhiN_fsg-ROCNcIUS6VuJ0c4CyTFBFymNA3AQbn0xpCgGYF3ezyfHEya9em6X0dZr6Y9WuY9Z1pgu3KNjrhbnKrMFWAe-N5lLx_-eLd6ev07OLV8nRxllopSJ9aS5TDiiCm8sxR61Tc1OUWcudUQZxBCERBsMsNxwVnOZGWEW4NExk1kh4lD3e6beWDHv8bNKaYMklkRiOx3BHOm2vddmVtuq_am1JvHb5badP1pa1ACwqCCS45kYpxFBPICy5BCc4JLySJWulOK3yGdsgnaqPrQ7RAc8EFySL_5I_88_JqsX19GHRsglAi4s_Gzwx5Dc5CE2taTaKmN0251iv_SWPGlNzmdzwKdP7jAKHXdRksVJVpwA9BZ0JxhBX_K4gFwRnPcAQf_QL-vsbzHbUysYxlU_iYno3LQV1a30BRRv8Cs0wJwtAm0ceTgMj08KVfmSEEvXx7-R_s-b-zF1dT9niPXYOp-nXw1dCXvglTkO1A2_kQOih-dAQjvZmz7zXRmznT45zFsAf73fwZNA4W_QapwCGi</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1313482863</pqid></control><display><type>article</type><title>Pseudo-messenger RNA: phantoms of the transcriptome</title><source>MEDLINE</source><source>DOAJ Directory of Open Access Journals</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>PubMed Central</source><source>SWEPUB Freely available online</source><source>Public Library of Science (PLoS)</source><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</creator><creatorcontrib>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</creatorcontrib><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><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 - genetics</subject><subject>Sequence Alignment</subject><subject>Transcription, Genetic</subject><issn>1553-7404</issn><issn>1553-7390</issn><issn>1553-7404</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><sourceid>D8T</sourceid><sourceid>DOA</sourceid><recordid>eNqVk22L1DAQx4so3nn6DUQXhAPBrnlsknshLOfTwnEnp97bkCbT3Z5tU5vWh29vdrfqVhSVBDJMfvPPZIZJkvsYzTEV-Om1H7rGVPN2Bc0cIRI3vZEcYs5pKhhiN_fsg-ROCNcIUS6VuJ0c4CyTFBFymNA3AQbn0xpCgGYF3ezyfHEya9em6X0dZr6Y9WuY9Z1pgu3KNjrhbnKrMFWAe-N5lLx_-eLd6ev07OLV8nRxllopSJ9aS5TDiiCm8sxR61Tc1OUWcudUQZxBCERBsMsNxwVnOZGWEW4NExk1kh4lD3e6beWDHv8bNKaYMklkRiOx3BHOm2vddmVtuq_am1JvHb5badP1pa1ACwqCCS45kYpxFBPICy5BCc4JLySJWulOK3yGdsgnaqPrQ7RAc8EFySL_5I_88_JqsX19GHRsglAi4s_Gzwx5Dc5CE2taTaKmN0251iv_SWPGlNzmdzwKdP7jAKHXdRksVJVpwA9BZ0JxhBX_K4gFwRnPcAQf_QL-vsbzHbUysYxlU_iYno3LQV1a30BRRv8Cs0wJwtAm0ceTgMj08KVfmSEEvXx7-R_s-b-zF1dT9niPXYOp-nXw1dCXvglTkO1A2_kQOih-dAQjvZmz7zXRmznT45zFsAf73fwZNA4W_QapwCGi</recordid><startdate>20060401</startdate><enddate>20060401</enddate><creator>Frith, Martin C</creator><creator>Wilming, Laurens G</creator><creator>Forrest, Alistair</creator><creator>Kawaji, Hideya</creator><creator>Tan, Sin Lam</creator><creator>Wahlestedt, Claes</creator><creator>Bajic, Vladimir B</creator><creator>Kai, Chikatoshi</creator><creator>Kawai, Jun</creator><creator>Carninci, Piero</creator><creator>Hayashizaki, Yoshihide</creator><creator>Bailey, Timothy L</creator><creator>Huminiecki, Lukasz</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>IOV</scope><scope>ISN</scope><scope>ISR</scope><scope>3V.</scope><scope>7QP</scope><scope>7QR</scope><scope>7SS</scope><scope>7TK</scope><scope>7TM</scope><scope>7TO</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>P64</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><scope>ADTPV</scope><scope>AOWAS</scope><scope>DF2</scope><scope>D8T</scope><scope>ZZAVC</scope><scope>DOA</scope></search><sort><creationdate>20060401</creationdate><title>Pseudo-messenger RNA: phantoms of the transcriptome</title><author>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</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c872t-cc29d192049b6d3cd9cd93dbcebdd9f2da00e7f21dba51f54b28c425ca4763a83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Animals</topic><topic>Bioinformatics - Computational Biology</topic><topic>Biotechnology</topic><topic>DNA Transposable Elements</topic><topic>Evolution</topic><topic>Evolution, Molecular</topic><topic>Genes</topic><topic>Genetics</topic><topic>Genetics/Gene Expression</topic><topic>Genomics</topic><topic>Homo (Human)</topic><topic>Humans</topic><topic>MEDICIN</topic><topic>MEDICINE</topic><topic>Messenger RNA</topic><topic>Mice</topic><topic>Mus (Mouse)</topic><topic>Promoter Regions, Genetic</topic><topic>Proteins</topic><topic>Proteins - genetics</topic><topic>Pseudogenes</topic><topic>Reproducibility of Results</topic><topic>Ribonucleic acid</topic><topic>RNA</topic><topic>RNA, Messenger - genetics</topic><topic>Sequence Alignment</topic><topic>Transcription, Genetic</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><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><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Opposing Viewpoints</collection><collection>Gale In Context: Canada</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>SwePub</collection><collection>SwePub Articles</collection><collection>SWEPUB Uppsala universitet</collection><collection>SWEPUB Freely available online</collection><collection>SwePub Articles full text</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PLoS genetics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Frith, Martin C</au><au>Wilming, Laurens G</au><au>Forrest, Alistair</au><au>Kawaji, Hideya</au><au>Tan, Sin Lam</au><au>Wahlestedt, Claes</au><au>Bajic, Vladimir B</au><au>Kai, Chikatoshi</au><au>Kawai, Jun</au><au>Carninci, Piero</au><au>Hayashizaki, Yoshihide</au><au>Bailey, Timothy L</au><au>Huminiecki, Lukasz</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pseudo-messenger RNA: phantoms of the transcriptome</atitle><jtitle>PLoS genetics</jtitle><addtitle>PLoS Genet</addtitle><date>2006-04-01</date><risdate>2006</risdate><volume>2</volume><issue>4</issue><spage>e23</spage><epage>e23</epage><pages>e23-e23</pages><issn>1553-7404</issn><issn>1553-7390</issn><eissn>1553-7404</eissn><abstract>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.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>16683022</pmid><doi>10.1371/journal.pgen.0020023</doi><tpages>504</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1553-7404
ispartof PLoS genetics, 2006-04, Vol.2 (4), p.e23-e23
issn 1553-7404
1553-7390
1553-7404
language eng
recordid cdi_plos_journals_1313482863
source MEDLINE; DOAJ Directory of Open Access Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central; SWEPUB Freely available online; Public Library of Science (PLoS)
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
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-09T21%3A04%3A35IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_plos_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Pseudo-messenger%20RNA:%20phantoms%20of%20the%20transcriptome&rft.jtitle=PLoS%20genetics&rft.au=Frith,%20Martin%20C&rft.date=2006-04-01&rft.volume=2&rft.issue=4&rft.spage=e23&rft.epage=e23&rft.pages=e23-e23&rft.issn=1553-7404&rft.eissn=1553-7404&rft_id=info:doi/10.1371/journal.pgen.0020023&rft_dat=%3Cgale_plos_%3EA146972402%3C/gale_plos_%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1313482863&rft_id=info:pmid/16683022&rft_galeid=A146972402&rft_doaj_id=oai_doaj_org_article_73e747585289450d9fbf58e975525f82&rfr_iscdi=true