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dc.contributor.authorSchwarz, Dianne S.
dc.contributor.authorHutvagner, Gyorgy
dc.contributor.authorDu, Tingting
dc.contributor.authorXu, Zuoshang
dc.contributor.authorAronin, Neil
dc.contributor.authorZamore, Phillip D.
dc.date2022-08-11T08:08:48.000
dc.date.accessioned2022-08-23T16:08:43Z
dc.date.available2022-08-23T16:08:43Z
dc.date.issued2003-10-22
dc.date.submitted2008-12-10
dc.identifier.citation<p>Cell. 2003 Oct 17;115(2):199-208.</p>
dc.identifier.issn0092-8674 (Print)
dc.identifier.doi10.1016/S0092-8674(03)00759-1
dc.identifier.pmid14567917
dc.identifier.urihttp://hdl.handle.net/20.500.14038/32517
dc.description.abstractA key step in RNA interference (RNAi) is assembly of the RISC, the protein-siRNA complex that mediates target RNA cleavage. Here, we show that the two strands of an siRNA duplex are not equally eligible for assembly into RISC. Rather, both the absolute and relative stabilities of the base pairs at the 5' ends of the two siRNA strands determine the degree to which each strand participates in the RNAi pathway. siRNA duplexes can be functionally asymmetric, with only one of the two strands able to trigger RNAi. Asymmetry is the hallmark of a related class of small, single-stranded, noncoding RNAs, microRNAs (miRNAs). We suggest that single-stranded miRNAs are initially generated as siRNA-like duplexes whose structures predestine one strand to enter the RISC and the other strand to be destroyed. Thus, the common step of RISC assembly is an unexpected source of asymmetry for both siRNA function and miRNA biogenesis.
dc.language.isoen_US
dc.relation<p><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=14567917&dopt=Abstract">Link to Article in PubMed</a></p>
dc.relation.urlhttps://doi.org/10.1016/S0092-8674(03)00759-1
dc.subjectAdenosine Diphosphate; Adenosine Triphosphate; Animals; Base Pair Mismatch; Base Pairing; Base Sequence; Drosophila melanogaster; Hydrogen Bonding; Kinetics; MicroRNAs; Models, Biological; Phosphorylation; RNA Helicases; *RNA Interference; RNA, Antisense; RNA, Double-Stranded; RNA, Messenger; RNA, Small Interfering; RNA, Untranslated; RNA-Induced Silencing Complex; Superoxide Dismutase
dc.subjectLife Sciences
dc.subjectMedicine and Health Sciences
dc.titleAsymmetry in the assembly of the RNAi enzyme complex
dc.typeJournal Article
dc.source.journaltitleCell
dc.source.volume115
dc.source.issue2
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/gsbs_sp/1084
dc.identifier.contextkey679622
html.description.abstract<p>A key step in RNA interference (RNAi) is assembly of the RISC, the protein-siRNA complex that mediates target RNA cleavage. Here, we show that the two strands of an siRNA duplex are not equally eligible for assembly into RISC. Rather, both the absolute and relative stabilities of the base pairs at the 5' ends of the two siRNA strands determine the degree to which each strand participates in the RNAi pathway. siRNA duplexes can be functionally asymmetric, with only one of the two strands able to trigger RNAi. Asymmetry is the hallmark of a related class of small, single-stranded, noncoding RNAs, microRNAs (miRNAs). We suggest that single-stranded miRNAs are initially generated as siRNA-like duplexes whose structures predestine one strand to enter the RISC and the other strand to be destroyed. Thus, the common step of RISC assembly is an unexpected source of asymmetry for both siRNA function and miRNA biogenesis.</p>
dc.identifier.submissionpathgsbs_sp/1084
dc.contributor.departmentDepartment of Medicine, Division of Endocrinology and Metabolism
dc.contributor.departmentDepartment of Biochemistry and Molecular Pharmacology
dc.contributor.departmentGraduate School of Biomedical Sciences
dc.source.pages199-208


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