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dc.contributor.authorShen, Haihong
dc.contributor.authorZheng, Xuexiu
dc.contributor.authorShen, Jingping
dc.contributor.authorZhang, Lingdi
dc.contributor.authorZhao, Rui
dc.contributor.authorGreen, Michael R.
dc.date2022-08-11T08:10:16.000
dc.date.accessioned2022-08-23T17:01:56Z
dc.date.available2022-08-23T17:01:56Z
dc.date.issued2008-07-03
dc.date.submitted2011-04-19
dc.identifier.citationGenes Dev. 2008 Jul 1;22(13):1796-803. <a href="http://dx.doi.org/10.1101/gad.1657308">Link to article on publisher's site</a>
dc.identifier.issn0890-9369 (Linking)
dc.identifier.doi10.1101/gad.1657308
dc.identifier.pmid18593880
dc.identifier.urihttp://hdl.handle.net/20.500.14038/44115
dc.description.abstractThe essential splicing factor human UAP56 (hUAP56) is a DExD/H-box protein known to promote prespliceosome assembly. Here, using a series of hUAP56 mutants that are defective for ATP-binding, ATP hydrolysis, or dsRNA unwindase/helicase activity, we assess the relative contributions of these biochemical functions to pre-mRNA splicing. We show that prespliceosome assembly requires hUAP56's ATP-binding and ATPase activities, which, unexpectedly, are required for hUAP56 to interact with U2AF(65) and be recruited into splicing complexes. Surprisingly, we find that hUAP56 is also required for mature spliceosome assembly, which requires, in addition to the ATP-binding and ATPase activities, hUAP56's dsRNA unwindase/helicase activity. We demonstrate that hUAP56 directly contacts U4 and U6 snRNAs and can promote unwinding of the U4/U6 duplex, and that both these activities are dependent on U2AF(65). Our results indicate that hUAP56 first interacts with U2AF(65) in an ATP-dependent manner, and subsequently with U4/U6 snRNAs to facilitate stepwise assembly of the spliceosome.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=18593880&dopt=Abstract">Link to Article in PubMed</a>
dc.relation.urlhttp://dx.doi.org/10.1101/gad.1657308
dc.subjectAdenosine Triphosphate
dc.subjectDEAD-box RNA Helicases
dc.subjectHela Cells
dc.subjectHumans
dc.subjectHydrolysis
dc.subjectMutation
dc.subjectNuclear Proteins
dc.subjectProtein Binding
dc.subjectRNA Precursors
dc.subjectRNA Splicing
dc.subjectRNA, Double-Stranded
dc.subjectRNA, Small Nuclear
dc.subjectRibonucleoprotein, U4-U6 Small Nuclear
dc.subjectRibonucleoproteins
dc.subjectSpliceosomes
dc.subjectGenetics and Genomics
dc.titleDistinct activities of the DExD/H-box splicing factor hUAP56 facilitate stepwise assembly of the spliceosome
dc.typeJournal Article
dc.source.journaltitleGenes and development
dc.source.volume22
dc.source.issue13
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/pgfe_pp/89
dc.identifier.contextkey1946744
html.description.abstract<p>The essential splicing factor human UAP56 (hUAP56) is a DExD/H-box protein known to promote prespliceosome assembly. Here, using a series of hUAP56 mutants that are defective for ATP-binding, ATP hydrolysis, or dsRNA unwindase/helicase activity, we assess the relative contributions of these biochemical functions to pre-mRNA splicing. We show that prespliceosome assembly requires hUAP56's ATP-binding and ATPase activities, which, unexpectedly, are required for hUAP56 to interact with U2AF(65) and be recruited into splicing complexes. Surprisingly, we find that hUAP56 is also required for mature spliceosome assembly, which requires, in addition to the ATP-binding and ATPase activities, hUAP56's dsRNA unwindase/helicase activity. We demonstrate that hUAP56 directly contacts U4 and U6 snRNAs and can promote unwinding of the U4/U6 duplex, and that both these activities are dependent on U2AF(65). Our results indicate that hUAP56 first interacts with U2AF(65) in an ATP-dependent manner, and subsequently with U4/U6 snRNAs to facilitate stepwise assembly of the spliceosome.</p>
dc.identifier.submissionpathpgfe_pp/89
dc.contributor.departmentProgram in Gene Function and Expression
dc.contributor.departmentProgram in Molecular Medicine
dc.source.pages1796-803


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