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dc.contributor.authorSharma, Upasna
dc.contributor.authorRando, Oliver J.
dc.date2022-08-11T08:09:21.000
dc.date.accessioned2022-08-23T16:27:09Z
dc.date.available2022-08-23T16:27:09Z
dc.date.issued2017-03-07
dc.date.submitted2017-05-25
dc.identifier.citationCell Metab. 2017 Mar 7;25(3):544-558. doi: 10.1016/j.cmet.2017.02.003. <a href="https://doi.org/10.1016/j.cmet.2017.02.003">Link to article on publisher's site</a>
dc.identifier.issn1550-4131 (Linking)
dc.identifier.doi10.1016/j.cmet.2017.02.003
dc.identifier.pmid28273477
dc.identifier.urihttp://hdl.handle.net/20.500.14038/36716
dc.description.abstractA number of molecular pathways play key roles in transmitting information in addition to the genomic sequence-epigenetic information-from one generation to the next. However, so-called epigenetic marks also impact an enormous variety of physiological processes, even under circumstances that do not result in heritable consequences. Perhaps inevitably, the epigenetic regulatory machinery is highly responsive to metabolic cues, as, for example, central metabolites are the substrates for the enzymes that catalyze the deposition of covalent modifications on histones, DNA, and RNA. Interestingly, in addition to the effects that metabolites exert over biological regulation in somatic cells, over the past decade multiple studies have shown that ancestral nutrition can alter the metabolic phenotype of offspring, raising the question of how metabolism regulates the epigenome of germ cells. Here, we review the widespread links between metabolism and epigenetic modifications, both in somatic cells and in the germline.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=28273477&dopt=Abstract">Link to Article in PubMed</a>
dc.relation.urlhttps://doi.org/10.1016/j.cmet.2017.02.003
dc.subjectBiochemistry
dc.subjectCell Biology
dc.subjectCellular and Molecular Physiology
dc.subjectMolecular Biology
dc.titleMetabolic Inputs into the Epigenome
dc.typeJournal Article
dc.source.journaltitleCell metabolism
dc.source.volume25
dc.source.issue3
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/metnet_pubs/84
dc.identifier.contextkey10212147
html.description.abstract<p>A number of molecular pathways play key roles in transmitting information in addition to the genomic sequence-epigenetic information-from one generation to the next. However, so-called epigenetic marks also impact an enormous variety of physiological processes, even under circumstances that do not result in heritable consequences. Perhaps inevitably, the epigenetic regulatory machinery is highly responsive to metabolic cues, as, for example, central metabolites are the substrates for the enzymes that catalyze the deposition of covalent modifications on histones, DNA, and RNA. Interestingly, in addition to the effects that metabolites exert over biological regulation in somatic cells, over the past decade multiple studies have shown that ancestral nutrition can alter the metabolic phenotype of offspring, raising the question of how metabolism regulates the epigenome of germ cells. Here, we review the widespread links between metabolism and epigenetic modifications, both in somatic cells and in the germline.</p>
dc.identifier.submissionpathmetnet_pubs/84
dc.contributor.departmentUMass Metabolic Network
dc.contributor.departmentDepartment of Biochemistry and Molecular Pharmacology
dc.source.pages544-558


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