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dc.contributor.authorTomari, Yukihide
dc.contributor.authorDu, Tingting
dc.contributor.authorHaley, Benjamin
dc.contributor.authorSchwarz, Dianne S.
dc.contributor.authorBennett, Ryan
dc.contributor.authorCook, Heather A.
dc.contributor.authorKoppetsch, Birgit S.
dc.contributor.authorTheurkauf, William E.
dc.contributor.authorZamore, Phillip D.
dc.date2022-08-11T08:08:49.000
dc.date.accessioned2022-08-23T16:09:27Z
dc.date.available2022-08-23T16:09:27Z
dc.date.issued2004-03-24
dc.date.submitted2009-01-13
dc.identifier.citation<p>Cell. 2004 Mar 19;116(6):831-41.</p>
dc.identifier.issn0092-8674 (Print)
dc.identifier.doi10.1016/S0092-8674(04)00218-1
dc.identifier.pmid15035985
dc.identifier.urihttp://hdl.handle.net/20.500.14038/32698
dc.description.abstractThe putative RNA helicase, Armitage (Armi), is required to repress oskar translation in Drosophila oocytes; armi mutant females are sterile and armi mutations disrupt anteroposterior and dorsoventral patterning. Here, we show that armi is required for RNAi. armi mutant male germ cells fail to silence Stellate, a gene regulated endogenously by RNAi, and lysates from armi mutant ovaries are defective for RNAi in vitro. Native gel analysis of protein-siRNA complexes in wild-type and armi mutant ovary lysates suggests that armi mutants support early steps in the RNAi pathway but are defective in the production of active RNA-induced silencing complex (RISC), which mediates target RNA destruction in RNAi. Our results suggest that armi is required for RISC maturation.
dc.language.isoen_US
dc.relation<p><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=15035985&dopt=Abstract">Link to Article in PubMed</a></p>
dc.relation.urlhttps://doi.org/10.1016/S0092-8674(04)00218-1
dc.subjectAnimals; Body Patterning; Cell Differentiation; Drosophila Proteins; Drosophila melanogaster; Embryo, Nonmammalian; Female; Germ Cells; Insect Proteins; Male; Mutation; Oocytes; Protein Kinases; RNA Helicases; RNA Interference; RNA, Small Interfering; RNA-Induced Silencing Complex
dc.subjectLife Sciences
dc.subjectMedicine and Health Sciences
dc.titleRISC assembly defects in the Drosophila RNAi mutant armitage
dc.typeJournal Article
dc.source.journaltitleCell
dc.source.volume116
dc.source.issue6
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/gsbs_sp/1255
dc.identifier.contextkey693166
html.description.abstract<p>The putative RNA helicase, Armitage (Armi), is required to repress oskar translation in Drosophila oocytes; armi mutant females are sterile and armi mutations disrupt anteroposterior and dorsoventral patterning. Here, we show that armi is required for RNAi. armi mutant male germ cells fail to silence Stellate, a gene regulated endogenously by RNAi, and lysates from armi mutant ovaries are defective for RNAi in vitro. Native gel analysis of protein-siRNA complexes in wild-type and armi mutant ovary lysates suggests that armi mutants support early steps in the RNAi pathway but are defective in the production of active RNA-induced silencing complex (RISC), which mediates target RNA destruction in RNAi. Our results suggest that armi is required for RISC maturation.</p>
dc.identifier.submissionpathgsbs_sp/1255
dc.contributor.departmentProgram in Molecular Medicine
dc.contributor.departmentDepartment of Biochemistry and Molecular Pharmacology
dc.contributor.departmentGraduate School of Biomedical Sciences
dc.source.pages831-41


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