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dc.contributor.authorWang, Yamei
dc.contributor.authorTissenbaum, Heidi A.
dc.date2022-08-11T08:10:15.000
dc.date.accessioned2022-08-23T17:00:59Z
dc.date.available2022-08-23T17:00:59Z
dc.date.issued2006-01-11
dc.date.submitted2011-04-19
dc.identifier.citationMech Ageing Dev. 2006 Jan;127(1):48-56. Epub 2005 Nov 8. <a href="http://dx.doi.org/10.1016/j.mad.2005.09.005">Link to article on publisher's site</a>
dc.identifier.issn0047-6374 (Linking)
dc.identifier.doi10.1016/j.mad.2005.09.005
dc.identifier.pmid16280150
dc.identifier.urihttp://hdl.handle.net/20.500.14038/43909
dc.description.abstractThe conserved SIR2 protein regulates life span in both yeast and worms: in both organisms overexpression of SIR2 can extend life span and in Caenorhabditis elegans this life span extension is dependent on the forkhead transcription factor, DAF-16. Here, we have done extensive genetic analysis with sir-2.1(ok434), a null mutant of C. elegans sir-2.1, the closest homolog to yeast Sir2p and human SIRT1 to further elucidate its function in life span regulation. sir-2.1(ok434) mutants show a slight decrease in life span as well as sensitivity to various stresses. Our genetic analysis suggests that sir-2.1 is required for life span extension by caloric restriction, independent of the insulin/IGF-1 signaling pathway. Importantly, analysis with unc-13 mutants indicates that sir-2.1 and daf-16 have overlapping and distinct roles in life span regulation. Our expression analysis shows that sir-2.1 has overlapping and distinct expression pattern compared with daf-16, consistent with the results from our genetic data. Our data defines a central role for C. elegans SIR2 in regulation of life span by caloric restriction and demonstrates that sir-2.1 and daf-16 have both overlapping and distinct functions in regulation of C. elegans life span.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=16280150&dopt=Abstract">Link to Article in PubMed</a>
dc.relation.urlhttp://dx.doi.org/10.1016/j.mad.2005.09.005
dc.subjectAging
dc.subjectAnimals
dc.subjectCaenorhabditis elegans
dc.subjectCaenorhabditis elegans Proteins
dc.subjectGene Expression Regulation
dc.subjectMutation
dc.subjectSirtuins
dc.subjectTime Factors
dc.subjectTranscription Factors
dc.subjectGenetics and Genomics
dc.titleOverlapping and distinct functions for a Caenorhabditis elegans SIR2 and DAF-16/FOXO
dc.typeJournal Article
dc.source.journaltitleMechanisms of ageing and development
dc.source.volume127
dc.source.issue1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/pgfe_pp/120
dc.identifier.contextkey1946775
html.description.abstract<p>The conserved SIR2 protein regulates life span in both yeast and worms: in both organisms overexpression of SIR2 can extend life span and in Caenorhabditis elegans this life span extension is dependent on the forkhead transcription factor, DAF-16. Here, we have done extensive genetic analysis with sir-2.1(ok434), a null mutant of C. elegans sir-2.1, the closest homolog to yeast Sir2p and human SIRT1 to further elucidate its function in life span regulation. sir-2.1(ok434) mutants show a slight decrease in life span as well as sensitivity to various stresses. Our genetic analysis suggests that sir-2.1 is required for life span extension by caloric restriction, independent of the insulin/IGF-1 signaling pathway. Importantly, analysis with unc-13 mutants indicates that sir-2.1 and daf-16 have overlapping and distinct roles in life span regulation. Our expression analysis shows that sir-2.1 has overlapping and distinct expression pattern compared with daf-16, consistent with the results from our genetic data. Our data defines a central role for C. elegans SIR2 in regulation of life span by caloric restriction and demonstrates that sir-2.1 and daf-16 have both overlapping and distinct functions in regulation of C. elegans life span.</p>
dc.identifier.submissionpathpgfe_pp/120
dc.contributor.departmentProgram in Gene Function and Expression
dc.source.pages48-56


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