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dc.contributor.authorYen, Kelvin
dc.contributor.authorNarasimhan, Sri Devi
dc.contributor.authorTissenbaum, Heidi A.
dc.date2022-08-11T08:10:16.000
dc.date.accessioned2022-08-23T17:01:41Z
dc.date.available2022-08-23T17:01:41Z
dc.date.issued2011-02-15
dc.date.submitted2011-04-19
dc.identifier.citationAntioxid Redox Signal. 2011 Feb 15;14(4):623-34. Epub 2010 Nov 30. <a href="http://dx.doi.org/10.1089/ars.2010.3490">Link to article on publisher's site</a>
dc.identifier.issn1523-0864 (Linking)
dc.identifier.doi10.1089/ars.2010.3490
dc.identifier.pmid20673162
dc.identifier.urihttp://hdl.handle.net/20.500.14038/44059
dc.description.abstractThe Caenorhabditis elegans Forkhead box O transcription factor (FOXO) homolog DAF-16 functions as a central mediator of multiple biological processes such as longevity, development, fat storage, stress resistance, and reproduction. In C. elegans, similar to other systems, DAF-16 functions as the downstream target of a conserved, well-characterized insulin/insulin-like growth factor (IGF)-1 signaling pathway. This cascade is comprised of an insulin/IGF-1 receptor, which signals through a conserved PI 3-kinase/AKT pathway that ultimately downregulates DAF-16/FOXO activity. Importantly, studies have shown that multiple pathways intersect with the insulin/IGF-1 signaling pathway and impinge on DAF-16 for their regulation. Therefore, in C. elegans, the single FOXO family member, DAF-16, integrates signals from several pathways and then regulates its many downstream target genes.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=20673162&dopt=Abstract">Link to Article in PubMed</a>
dc.relation.urlhttp://dx.doi.org/10.1089/ars.2010.3490
dc.rights<p>This is a copy of an article published in Antioxidants & Redox Signaling © 2010 Mary Ann Liebert, Inc. and available online at: http://www.liebertonline.com.</p>
dc.subjectCaenorhabditis elegans Proteins
dc.subjectTranscription Factors
dc.subjectForkhead Transcription Factors
dc.subjectInsulin-Like Growth Factor I
dc.subjectReceptor, IGF Type 1
dc.subjectGenetics and Genomics
dc.titleDAF-16/Forkhead box O transcription factor: many paths to a single Fork(head) in the road
dc.typeJournal Article
dc.source.journaltitleAntioxidants and redox signaling
dc.source.volume14
dc.source.issue4
dc.identifier.legacyfulltexthttps://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=1034&amp;context=pgfe_pp&amp;unstamped=1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/pgfe_pp/34
dc.identifier.contextkey1946687
refterms.dateFOA2022-08-23T17:01:41Z
html.description.abstract<p>The Caenorhabditis elegans Forkhead box O transcription factor (FOXO) homolog DAF-16 functions as a central mediator of multiple biological processes such as longevity, development, fat storage, stress resistance, and reproduction. In C. elegans, similar to other systems, DAF-16 functions as the downstream target of a conserved, well-characterized insulin/insulin-like growth factor (IGF)-1 signaling pathway. This cascade is comprised of an insulin/IGF-1 receptor, which signals through a conserved PI 3-kinase/AKT pathway that ultimately downregulates DAF-16/FOXO activity. Importantly, studies have shown that multiple pathways intersect with the insulin/IGF-1 signaling pathway and impinge on DAF-16 for their regulation. Therefore, in C. elegans, the single FOXO family member, DAF-16, integrates signals from several pathways and then regulates its many downstream target genes.</p>
dc.identifier.submissionpathpgfe_pp/34
dc.contributor.departmentProgram in Gene Function and Expression
dc.source.pages623-34


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