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dc.contributor.authorRando, Oliver J.
dc.contributor.authorChang, Howard Y.
dc.date2022-08-11T08:09:39.000
dc.date.accessioned2022-08-23T16:38:38Z
dc.date.available2022-08-23T16:38:38Z
dc.date.issued2009-03-26
dc.date.submitted2010-03-26
dc.identifier.citation<p>Annu Rev Biochem. 2009;78:245-71. <a href="http://dx.doi.org/10.1146/annurev.biochem.78.071107.134639">Link to article on publisher's site</a></p>
dc.identifier.issn0066-4154 (Linking)
dc.identifier.doi10.1146/annurev.biochem.78.071107.134639
dc.identifier.pmid19317649
dc.identifier.urihttp://hdl.handle.net/20.500.14038/39291
dc.description.abstractEukaryotic genomes are packaged into a nucleoprotein complex known as chromatin, which affects most processes that occur on DNA. Along with genetic and biochemical studies of resident chromatin proteins and their modifying enzymes, mapping of chromatin structure in vivo is one of the main pillars in our understanding of how chromatin relates to cellular processes. In this review, we discuss the use of genomic technologies to characterize chromatin structure in vivo, with a focus on data from budding yeast and humans. The picture emerging from these studies is the detailed chromatin structure of a typical gene, where the typical behavior gives insight into the mechanisms and deep rules that establish chromatin structure. Important deviation from the archetype is also observed, usually as a consequence of unique regulatory mechanisms at special genomic loci. Chromatin structure shows substantial conservation from yeast to humans, but mammalian chromatin has additional layers of complexity that likely relate to the requirements of multicellularity such as the need to establish faithful gene regulatory mechanisms for cell differentiation.
dc.language.isoen_US
dc.relation<p><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=19317649&dopt=Abstract">Link to Article in PubMed</a></p>
dc.relation.urlhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2811691/
dc.subjectAnimals
dc.subjectChromatin
dc.subjectChromatin Assembly and Disassembly
dc.subjectGene Expression
dc.subject*Genome
dc.subjectGenome, Human
dc.subjectHumans
dc.subjectSaccharomyces cerevisiae
dc.subjectLife Sciences
dc.subjectMedicine and Health Sciences
dc.titleGenome-wide views of chromatin structure
dc.typeJournal Article
dc.source.journaltitleAnnual review of biochemistry
dc.source.volume78
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/oapubs/2090
dc.identifier.contextkey1246892
html.description.abstract<p>Eukaryotic genomes are packaged into a nucleoprotein complex known as chromatin, which affects most processes that occur on DNA. Along with genetic and biochemical studies of resident chromatin proteins and their modifying enzymes, mapping of chromatin structure in vivo is one of the main pillars in our understanding of how chromatin relates to cellular processes. In this review, we discuss the use of genomic technologies to characterize chromatin structure in vivo, with a focus on data from budding yeast and humans. The picture emerging from these studies is the detailed chromatin structure of a typical gene, where the typical behavior gives insight into the mechanisms and deep rules that establish chromatin structure. Important deviation from the archetype is also observed, usually as a consequence of unique regulatory mechanisms at special genomic loci. Chromatin structure shows substantial conservation from yeast to humans, but mammalian chromatin has additional layers of complexity that likely relate to the requirements of multicellularity such as the need to establish faithful gene regulatory mechanisms for cell differentiation.</p>
dc.identifier.submissionpathoapubs/2090
dc.contributor.departmentDepartment of Biochemistry and Molecular Pharmacology
dc.source.pages245-71


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