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dc.contributor.authorDekker, Job
dc.date2022-08-11T08:11:00.000
dc.date.accessioned2022-08-23T17:27:47Z
dc.date.available2022-08-23T17:27:47Z
dc.date.issued2003-06-27
dc.date.submitted2012-08-10
dc.identifier.citationTrends Biochem Sci. 2003 Jun;28(6):277-80. <a href="http://dx.doi.org/10.1016/S0968-0004(03)00089-6">Link to article on publisher's site</a>
dc.identifier.issn0968-0004 (Linking)
dc.identifier.doi10.1016/S0968-0004(03)00089-6
dc.identifier.pmid12826398
dc.identifier.urihttp://hdl.handle.net/20.500.14038/49939
dc.description.abstractHigher-order chromosome organization is emerging as a major determinant of gene regulation. Although the structure of chromatin at the level of individual nucleosomes has been studied in considerable detail, less is known about higher levels of organization. Two new methods have been developed that can be used to obtain detailed information about the higher-order folding of chromatin. Using these methods, long-range looping interactions have been shown to occur upon activation of the murine beta-globin locus, explaining the long-standing question of how gene regulatory elements can act at large genomic distances from their 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=12826398&dopt=Abstract">Link to Article in PubMed</a>
dc.relation.urlhttp://dx.doi.org/10.1016/S0968-0004(03)00089-6
dc.subjectAnimals
dc.subjectBinding Sites
dc.subjectChromatin
dc.subjectChromosome Mapping
dc.subjectDNA
dc.subjectGlobins
dc.subjectHumans
dc.subjectLocus Control Region
dc.subjectBiochemistry, Biophysics, and Structural Biology
dc.subjectGenetics and Genomics
dc.subjectSystems Biology
dc.titleA closer look at long-range chromosomal interactions
dc.typeJournal Article
dc.source.journaltitleTrends in biochemical sciences
dc.source.volume28
dc.source.issue6
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/sysbio_pubs/6
dc.identifier.contextkey3201823
html.description.abstract<p>Higher-order chromosome organization is emerging as a major determinant of gene regulation. Although the structure of chromatin at the level of individual nucleosomes has been studied in considerable detail, less is known about higher levels of organization. Two new methods have been developed that can be used to obtain detailed information about the higher-order folding of chromatin. Using these methods, long-range looping interactions have been shown to occur upon activation of the murine beta-globin locus, explaining the long-standing question of how gene regulatory elements can act at large genomic distances from their target genes.</p>
dc.identifier.submissionpathsysbio_pubs/6
dc.contributor.departmentDepartment of Biochemistry and Molecular Pharmacology
dc.contributor.departmentProgram in Systems Biology
dc.contributor.departmentProgram in Gene Function and Expression
dc.source.pages277-80


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