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dc.contributor.authorJungreis, Irwin
dc.contributor.authorLin, Michael F.
dc.contributor.authorSpokony, Rebecca
dc.contributor.authorChan, Clara Sophia
dc.contributor.authorNegre, Nicolas
dc.contributor.authorVictorsen, Alec
dc.contributor.authorWhite, Kevin P.
dc.contributor.authorKellis, Manolis
dc.date.accessioned2012-09-18T15:15:14Z
dc.date.available2012-09-18T15:15:14Z
dc.date.issued2011-10
dc.date.submitted2010-12
dc.identifier.issn1088-9051
dc.identifier.urihttp://hdl.handle.net/1721.1/73035
dc.description.abstractWhile translational stop codon readthrough is often used by viral genomes, it has been observed for only a handful of eukaryotic genes. We previously used comparative genomics evidence to recognize protein-coding regions in 12 species of Drosophila and showed that for 149 genes, the open reading frame following the stop codon has a protein-coding conservation signature, hinting that stop codon readthrough might be common in Drosophila. We return to this observation armed with deep RNA sequence data from the modENCODE project, an improved higher-resolution comparative genomics metric for detecting protein-coding regions, comparative sequence information from additional species, and directed experimental evidence. We report an expanded set of 283 readthrough candidates, including 16 double-readthrough candidates; these were manually curated to rule out alternatives such as A-to-I editing, alternative splicing, dicistronic translation, and selenocysteine incorporation. We report experimental evidence of translation using GFP tagging and mass spectrometry for several readthrough regions. We find that the set of readthrough candidates differs from other genes in length, composition, conservation, stop codon context, and in some cases, conserved stem–loops, providing clues about readthrough regulation and potential mechanisms. Lastly, we expand our studies beyond Drosophila and find evidence of abundant readthrough in several other insect species and one crustacean, and several readthrough candidates in nematode and human, suggesting that functionally important translational stop codon readthrough is significantly more prevalent in Metazoa than previously recognized.en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (U54 HG00455-01)en_US
dc.description.sponsorshipNational Science Foundation (U.S.) (CAREER 0644282)en_US
dc.description.sponsorshipAlfred P. Sloan Foundationen_US
dc.language.isoen_US
dc.publisherCold Spring Harbor Laboratory Pressen_US
dc.relation.isversionofhttp://dx.doi.org/ 10.1101/gr.119974.110en_US
dc.rightsCreative Commons Attribution-NonCommercial 3.0 Unported Licenseen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc/3.0/en_US
dc.sourceGenome Researchen_US
dc.titleEvidence of abundant stop codon readthrough in Drosophila and other Metazoaen_US
dc.typeArticleen_US
dc.identifier.citationJungreis, I. et al. “Evidence of Abundant Stop Codon Readthrough in Drosophila and Other Metazoa.” Genome Research 21.12 (2011): 2096–2113. © 2011 by Cold Spring Harbor Laboratory Pressen_US
dc.contributor.departmentMassachusetts Institute of Technology. Computer Science and Artificial Intelligence Laboratoryen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biologyen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Electrical Engineering and Computer Scienceen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Mathematicsen_US
dc.contributor.mitauthorJungreis, Irwin
dc.contributor.mitauthorLin, Michael F.
dc.contributor.mitauthorChan, Clara Sophia
dc.contributor.mitauthorKellis, Manolis
dc.relation.journalGenome Researchen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsJungreis, I.; Lin, M. F.; Spokony, R.; Chan, C. S.; Negre, N.; Victorsen, A.; White, K. P.; Kellis, M.en
dc.identifier.orcidhttps://orcid.org/0000-0002-7852-4328
mit.licensePUBLISHER_CCen_US
mit.metadata.statusComplete


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