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dc.contributor.author Seo, Mihwa -
dc.contributor.author Park, Sangsoon -
dc.contributor.author Nam, Hong Gil -
dc.contributor.author Lee, Seung-Jae V. -
dc.date.available 2017-05-11T01:46:39Z -
dc.date.created 2017-04-10 -
dc.date.issued 2016 -
dc.identifier.issn 1538-4101 -
dc.identifier.uri http://hdl.handle.net/20.500.11750/1649 -
dc.description.abstract ABSTRACT: RNA helicases, which unwind RNAs, are essential for RNA metabolism and homeostasis. However, the roles of RNA helicases in specific physiological processes remain poorly understood. We recently reported that an RNA helicase, HEL-1, promotes long lifespan conferred by reduced insulin/insulin-like growth factor-1 (IGF-1) signaling (IIS) in Caenorhabditis elegans. We also showed that HEL-1 induces the expression of longevity genes by physically interacting with Forkhead box O (FOXO) transcription factor. Thus, the HEL-1 RNA helicase appears to regulate lifespan by specifically activating FOXO in IIS. In the current study, we report another longevity-promoting RNA helicase, Suppressor of ACY-4 sterility 1 (SACY-1). SACY-1 contributed to the longevity of daf-2/insulin/IGF-1 receptor mutants. Unlike HEL-1, SACY-1 was also required for the longevity due to mutations in genes involved in non-IIS pathways. Thus, SACY-1 appears to function as a general longevity factor for various signaling pathways, which is different from the specific function of HEL-1. © 2016 Taylor & Francis. -
dc.language English -
dc.publisher Taylor and Francis Ltd. -
dc.title RNA helicase SACY-1 is required for longevity caused by various genetic perturbations in Caenorhabditis elegans -
dc.type Article -
dc.identifier.doi 10.1080/15384101.2016.1183845 -
dc.identifier.scopusid 2-s2.0-84973174670 -
dc.identifier.bibliographicCitation Cell Cycle, v.15, no.14, pp.1821 - 1829 -
dc.description.isOpenAccess FALSE -
dc.subject.keywordAuthor Aging -
dc.subject.keywordAuthor daf-2 -
dc.subject.keywordAuthor C -
dc.subject.keywordAuthor elegans -
dc.subject.keywordAuthor HEL-1 -
dc.subject.keywordAuthor insulin -
dc.subject.keywordAuthor IGF-1 signaling -
dc.subject.keywordAuthor RNA helicase -
dc.subject.keywordAuthor SACY-1 -
dc.subject.keywordPlus Aging -
dc.subject.keywordPlus Amino ACID Sequence -
dc.subject.keywordPlus Binding -
dc.subject.keywordPlus C -
dc.subject.keywordPlus C. Elegans -
dc.subject.keywordPlus Caenorhabditis Elegans -
dc.subject.keywordPlus Controlled Study -
dc.subject.keywordPlus DAF-16 -
dc.subject.keywordPlus DAF-2 -
dc.subject.keywordPlus DDX41 -
dc.subject.keywordPlus ELEGANS -
dc.subject.keywordPlus FAMILY -
dc.subject.keywordPlus Gene Mutation -
dc.subject.keywordPlus Heat Stress -
dc.subject.keywordPlus HEL-1 -
dc.subject.keywordPlus Igf-1 Signaling -
dc.subject.keywordPlus Insulin/IGF-1 Signaling -
dc.subject.keywordPlus LIFE-SPAN -
dc.subject.keywordPlus LONGEVITY -
dc.subject.keywordPlus Nonhuman -
dc.subject.keywordPlus Note -
dc.subject.keywordPlus OXIDATIVE STRESS -
dc.subject.keywordPlus PATHWAYS -
dc.subject.keywordPlus RNA Helicase -
dc.subject.keywordPlus RNA Helicase Suppressor of Acy 4 Sterility 1 -
dc.subject.keywordPlus SACY-1 -
dc.subject.keywordPlus Unclassified Drug -
dc.subject.keywordPlus IMMUNITY -
dc.subject.keywordPlus INHIBITION -
dc.subject.keywordPlus Insulin -
dc.subject.keywordPlus Insulin/IGF-1 -
dc.citation.endPage 1829 -
dc.citation.number 14 -
dc.citation.startPage 1821 -
dc.citation.title Cell Cycle -
dc.citation.volume 15 -
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Department of New Biology CBRG(Complex Biology Research Group) 1. Journal Articles

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