Overlapping and distinct functions for a Caenorhabditis elegans SIR2 and DAF-16/FOXO
| dc.contributor.author | Wang, Yamei | |
| dc.contributor.author | Tissenbaum, Heidi A. | |
| dc.date | 2022-08-11T08:10:15.000 | |
| dc.date.accessioned | 2022-08-23T17:00:59Z | |
| dc.date.available | 2022-08-23T17:00:59Z | |
| dc.date.issued | 2006-01-11 | |
| dc.date.submitted | 2011-04-19 | |
| dc.identifier.citation | Mech 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.issn | 0047-6374 (Linking) | |
| dc.identifier.doi | 10.1016/j.mad.2005.09.005 | |
| dc.identifier.pmid | 16280150 | |
| dc.identifier.uri | http://hdl.handle.net/20.500.14038/43909 | |
| dc.description.abstract | 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. | |
| dc.language.iso | en_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.url | http://dx.doi.org/10.1016/j.mad.2005.09.005 | |
| dc.subject | Aging | |
| dc.subject | Animals | |
| dc.subject | Caenorhabditis elegans | |
| dc.subject | Caenorhabditis elegans Proteins | |
| dc.subject | Gene Expression Regulation | |
| dc.subject | Mutation | |
| dc.subject | Sirtuins | |
| dc.subject | Time Factors | |
| dc.subject | Transcription Factors | |
| dc.subject | Genetics and Genomics | |
| dc.title | Overlapping and distinct functions for a Caenorhabditis elegans SIR2 and DAF-16/FOXO | |
| dc.type | Journal Article | |
| dc.source.journaltitle | Mechanisms of ageing and development | |
| dc.source.volume | 127 | |
| dc.source.issue | 1 | |
| dc.identifier.legacycoverpage | https://escholarship.umassmed.edu/pgfe_pp/120 | |
| dc.identifier.contextkey | 1946775 | |
| 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.submissionpath | pgfe_pp/120 | |
| dc.contributor.department | Program in Gene Function and Expression | |
| dc.source.pages | 48-56 |