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dc.contributor.authorMacNeil, Lesley T.
dc.contributor.authorWatson, Emma
dc.contributor.authorArda, H. Efsun
dc.contributor.authorZhu, Lihua Julie
dc.contributor.authorWalhout, Albertha J. M.
dc.date2022-08-11T08:11:00.000
dc.date.accessioned2022-08-23T17:27:38Z
dc.date.available2022-08-23T17:27:38Z
dc.date.issued2013-03-28
dc.date.submitted2013-04-23
dc.identifier.citationCell. 2013 Mar 28;153(1):240-52. doi: 10.1016/j.cell.2013.02.049. <a href="http://dx.doi.org/10.1016/j.cell.2013.02.049" target="_blank"> Link to article on publisher's website</a></p>
dc.identifier.issn1097-4172
dc.identifier.doi10.1016/j.cell.2013.02.049
dc.identifier.pmid23540701
dc.identifier.urihttp://hdl.handle.net/20.500.14038/49906
dc.description.abstractDietary composition has major effects on physiology. Here, we show that developmental rate, reproduction, and lifespan are altered in C. elegans fed Comamonas DA1877 relative to those fed a standard E. coli OP50 diet. We identify a set of genes that change in expression in response to this diet and use the promoter of one of these (acdh-1) as a dietary sensor. Remarkably, the effects on transcription and development occur even when Comamonas DA1877 is diluted with another diet, suggesting that Comamonas DA1877 generates a signal that is sensed by the nematode. Surprisingly, the developmental effect is independent from TOR and insulin signaling. Rather, Comamonas DA1877 affects cyclic gene expression during molting, likely through the nuclear hormone receptor NHR-23. Altogether, our findings indicate that different bacteria elicit various responses via distinct mechanisms, which has implications for diseases such as obesity and the interactions between the human microbiome and intestinal cells.
dc.language.isoen_US
dc.publisherCell Press
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=23540701&dopt=Abstract">Link to article in PubMed</a>
dc.relation.urlhttp://dx.doi.org/10.1016/j.cell.2013.02.049
dc.subjectCaenorhabditis elegans
dc.subjectCaenorhabditis elegans Proteins
dc.subjectInsulin
dc.subjectGene Expression Regulation, Developmental
dc.subjectDiet
dc.subjectBiochemical Phenomena, Metabolism, and Nutrition
dc.subjectCell and Developmental Biology
dc.subjectGenetics and Genomics
dc.subjectSystems Biology
dc.titleDiet-Induced Developmental Acceleration Independent of TOR and Insulin in C. elegans
dc.typeJournal Article
dc.source.journaltitleCell
dc.source.volume153
dc.source.issue1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/sysbio_pubs/24
dc.identifier.contextkey4060070
html.description.abstract<p>Dietary composition has major effects on physiology. Here, we show that developmental rate, reproduction, and lifespan are altered in C. elegans fed Comamonas DA1877 relative to those fed a standard E. coli OP50 diet. We identify a set of genes that change in expression in response to this diet and use the promoter of one of these (acdh-1) as a dietary sensor. Remarkably, the effects on transcription and development occur even when Comamonas DA1877 is diluted with another diet, suggesting that Comamonas DA1877 generates a signal that is sensed by the nematode. Surprisingly, the developmental effect is independent from TOR and insulin signaling. Rather, Comamonas DA1877 affects cyclic gene expression during molting, likely through the nuclear hormone receptor NHR-23. Altogether, our findings indicate that different bacteria elicit various responses via distinct mechanisms, which has implications for diseases such as obesity and the interactions between the human microbiome and intestinal cells.</p>
dc.identifier.submissionpathsysbio_pubs/24
dc.contributor.departmentProgram in Gene Function and Expression
dc.contributor.departmentProgram in Molecular Medicine
dc.contributor.departmentProgram in Systems Biology
dc.source.pages240-52


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