Global Patterns of Tissue-Specific Alternative Polyadenylation in Drosophila

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dc.contributor.authorSmibert, P.
dc.contributor.authorMiura, P.
dc.contributor.authorWestholm, J.O.
dc.contributor.authorShenker, S.
dc.contributor.authorMay, G.
dc.contributor.authorDuff, M.O.
dc.contributor.authorZhang, D.
dc.contributor.authorEads, B.D.
dc.contributor.authorCarlson, J.
dc.contributor.authorBrown, J.B.
dc.contributor.authorEisman, R.C.
dc.contributor.authorAndrews, J.
dc.contributor.authorKaufman, T.
dc.contributor.authorCherbas, P.
dc.contributor.authorCelniker, S.E.
dc.contributor.authorGraveley, B.R.
dc.contributor.authorLai, E.C.
dc.date.accessioned2014-12-09T19:46:38Z
dc.date.available2014-12-09T19:46:38Z
dc.date.issued2012
dc.description.abstractWe analyzed the usage and consequences of alternative cleavage and polyadenylation (APA) in $\textit{Drosophila melanogaster}$ by using >1 billion reads of stranded mRNA-seq across a variety of dissected tissues. Beyond demonstrating that a majority of fly transcripts are subject to APA, we observed broad trends for 3′ untranslated region (UTR) shortening in the testis and lengthening in the central nervous system (CNS); the latter included hundreds of unannotated extensions ranging up to 18 kb. Extensive northern analyses validated the accumulation of full-length neural extended transcripts, and in situ hybridization indicated their spatial restriction to the CNS. Genes encoding RNA binding proteins (RBPs) and transcription factors were preferentially subject to 3′ UTR extensions. Motif analysis indicated enrichment of miRNA and RBP sites in the neural extensions, and their termini were enriched in canonical cis elements that promote cleavage and polyadenylation. Altogether, we reveal broad tissue-specific patterns of APA in $\textit{Drosophila}$ and transcripts with unprecedented 3′ UTR length in the nervous system.
dc.identifier.citationSmibert, P., Miura, P., Westholm, J. O., Shenker, S., May, G., Duff, M. O., . . . Lai, E. C. (2012). Global patterns of tissue-specific alternative polyadenylation in drosophila. Cell Reports, 1(3), 277-289. http://dx.doi.org/10.1016/j.celrep.2012.01.001
dc.identifier.urihttps://hdl.handle.net/2022/19197
dc.language.isoen_US
dc.publisherCell Reports
dc.relation.isversionofhttps://doi.org/10.1016/j.celrep.2012.01.001
dc.rights© 2012 The Authors
dc.subjectmicroRNA
dc.subjectRNA binding protein
dc.subject3' untranslated region
dc.subjectalternative cleavage and polyadenylation
dc.subjectbinding site
dc.subjectDrosophila melanogaster
dc.subjectgene expression
dc.subjectin situ hybridization
dc.subjectnonhuman
dc.subjectNorthern blotting
dc.subjectpolyadenylation
dc.subjectprotein motif
dc.subjectRNA sequence
dc.subjecttissue specificity
dc.subjecttranscription regulation
dc.subjectAnimals
dc.subjectBase Sequence
dc.subjectBlotting, Northern
dc.subjectConserved Sequence
dc.subjectDNA-Binding Proteins
dc.subjectDrosophila melanogaster
dc.subjectEmbryo, Nonmammalian
dc.subjectGene Expression Regulation, Developmental
dc.subjectGenes, Insect
dc.subjectmale
dc.subjectMolecular Sequence Data
dc.subjectNeurons
dc.subjectNucleotide Motifs
dc.subjectOrgan Specificity
dc.subjectPoly A
dc.subjectpolyadenylation
dc.subjectProtein Isoforms
dc.subjectReproducibility of Results
dc.subjectRNA, Messenger
dc.subjectSequence Analysis, RNA
dc.subjectTestis
dc.subjectTranscriptome
dc.titleGlobal Patterns of Tissue-Specific Alternative Polyadenylation in Drosophila
dc.typeArticle

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