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dc.contributor.authorMunroe, David
dc.contributor.authorJacobson, Allan
dc.date2022-08-11T08:09:02.000
dc.date.accessioned2022-08-23T16:16:01Z
dc.date.available2022-08-23T16:16:01Z
dc.date.issued1990-07-16
dc.date.submitted2008-11-24
dc.identifier.citationGene. 1990 Jul 16;91(2):151-8.
dc.identifier.issn0378-1119 (Print)
dc.identifier.pmid1976572
dc.identifier.urihttp://hdl.handle.net/20.500.14038/34231
dc.description.abstractUntil recently, evidence to support a translational role for the 3'-poly(A) tract of eukaryotic mRNAs has been mostly indirect, including: a correlation between the adenylation status of individual mRNAs and their translatability in vivo or in vitro, the demonstration that exogenously added poly(A) is a potent competitive inhibitor of the translation of poly(A)+mRNA, but not poly(A)-mRNAs in vitro, and a correlation between the abundance and stability of poly(A)-binding proteins (PABPs) and the rate of translational initiation in vivo. However, more recent studies demonstrate directly that poly(A)+mRNAs can initiate translation more efficiently than poly(A)-mRNAs, and indicate that this effect is: (i) targeted to the formation of 80S initiation complexes, and (ii) likely to be mediated by the cytoplasmic PABP. We suggest that the 3'-poly(A) tail should be considered a translational enhancer which may stimulate translational initiation in much the same way that transcriptional enhancers are thought to stimulate transcriptional initiation.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=1976572&dopt=Abstract">Link to article in PubMed</a>
dc.relation.urlhttp://dx.doi.org/10.1016/0378-1119(90)90082-3
dc.subjectAnimals; Carrier Proteins; Cytoplasm; Gene Expression Regulation; Models, Genetic; Poly A; *Protein Biosynthesis; RNA, Messenger
dc.subjectLife Sciences
dc.subjectMedicine and Health Sciences
dc.titleTales of poly(A): a review
dc.typeJournal Article
dc.source.journaltitleGene
dc.source.volume91
dc.source.issue2
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/gsbs_sp/888
dc.identifier.contextkey671451
html.description.abstract<p>Until recently, evidence to support a translational role for the 3'-poly(A) tract of eukaryotic mRNAs has been mostly indirect, including: a correlation between the adenylation status of individual mRNAs and their translatability in vivo or in vitro, the demonstration that exogenously added poly(A) is a potent competitive inhibitor of the translation of poly(A)+mRNA, but not poly(A)-mRNAs in vitro, and a correlation between the abundance and stability of poly(A)-binding proteins (PABPs) and the rate of translational initiation in vivo. However, more recent studies demonstrate directly that poly(A)+mRNAs can initiate translation more efficiently than poly(A)-mRNAs, and indicate that this effect is: (i) targeted to the formation of 80S initiation complexes, and (ii) likely to be mediated by the cytoplasmic PABP. We suggest that the 3'-poly(A) tail should be considered a translational enhancer which may stimulate translational initiation in much the same way that transcriptional enhancers are thought to stimulate transcriptional initiation.</p>
dc.identifier.submissionpathgsbs_sp/888
dc.contributor.departmentDepartment of Molecular Genetics and Microbiology
dc.contributor.departmentGraduate School of Biomedical Sciences
dc.source.pages151-8


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