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dc.contributor.authorWatson, Emma
dc.contributor.authorMacNeil, Lesley T.
dc.contributor.authorArda, H. Efsun
dc.contributor.authorZhu, Lihua Julie
dc.contributor.authorWalhout, Albertha J. M.
dc.date2022-08-11T08:10:59.000
dc.date.accessioned2022-08-23T17:27:37Z
dc.date.available2022-08-23T17:27:37Z
dc.date.issued2013-03-28
dc.date.submitted2013-04-08
dc.identifier.citationCell. 2013 Mar 28;153(1):253-66. doi: 10.1016/j.cell.2013.02.050. <a href="http://dx.doi.org/10.1016/j.cell.2013.02.050" target="_blank">Link to article on publisher's site</a></p>
dc.identifier.issn0092-8674 (Linking)
dc.identifier.doi10.1016/j.cell.2013.02.050
dc.identifier.pmid23540702
dc.identifier.urihttp://hdl.handle.net/20.500.14038/49903
dc.description.abstractExpression profiles are tailored according to dietary input. However, the networks that control dietary responses remain largely uncharacterized. Here, we combine forward and reverse genetic screens to delineate a network of 184 genes that affect the C. elegans dietary response to Comamonas DA1877 bacteria. We find that perturbation of a mitochondrial network composed of enzymes involved in amino acid metabolism and the TCA cycle affects the dietary response. In humans, mutations in the corresponding genes cause inborn diseases of amino acid metabolism, most of which are treated by dietary intervention. We identify several transcription factors (TFs) that mediate the changes in gene expression upon metabolic network perturbations. Altogether, our findings unveil a transcriptional response system that is poised to sense dietary cues and metabolic imbalances, illustrating extensive communication between metabolic networks in the mitochondria and gene regulatory networks in the nucleus.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=23540702&dopt=Abstract">Link to Article in PubMed</a>
dc.relation.urlhttp://dx.doi.org/10.1016/j.cell.2013.02.050
dc.subjectGene Regulatory Networks
dc.subjectMetabolic Networks and Pathways
dc.subjectCaenorhabditis elegans
dc.subjectBiochemical Phenomena, Metabolism, and Nutrition
dc.subjectGenetics and Genomics
dc.subjectSystems Biology
dc.titleIntegration of Metabolic and Gene Regulatory Networks Modulates the C. elegans Dietary Response
dc.typeJournal Article
dc.source.journaltitleCell
dc.source.volume153
dc.source.issue1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/sysbio_pubs/21
dc.identifier.contextkey4007876
html.description.abstract<p>Expression profiles are tailored according to dietary input. However, the networks that control dietary responses remain largely uncharacterized. Here, we combine forward and reverse genetic screens to delineate a network of 184 genes that affect the C. elegans dietary response to Comamonas DA1877 bacteria. We find that perturbation of a mitochondrial network composed of enzymes involved in amino acid metabolism and the TCA cycle affects the dietary response. In humans, mutations in the corresponding genes cause inborn diseases of amino acid metabolism, most of which are treated by dietary intervention. We identify several transcription factors (TFs) that mediate the changes in gene expression upon metabolic network perturbations. Altogether, our findings unveil a transcriptional response system that is poised to sense dietary cues and metabolic imbalances, illustrating extensive communication between metabolic networks in the mitochondria and gene regulatory networks in the nucleus.</p>
dc.identifier.submissionpathsysbio_pubs/21
dc.contributor.departmentProgram in Molecular Medicine
dc.contributor.departmentProgram in Gene Function and Expression
dc.contributor.departmentProgram in Systems Biology
dc.source.pages253-66


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