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dc.contributor.authorUmbarger, Mark A.
dc.contributor.authorToro, Esteban
dc.contributor.authorWright, Matthew A.
dc.contributor.authorPorreca, Gregory J.
dc.contributor.authorBau, Davide
dc.contributor.authorHong, Sun-Hae
dc.contributor.authorFero, Michael J.
dc.contributor.authorZhu, Lihua Julie
dc.contributor.authorMarti-Renom, Marc A.
dc.contributor.authorMcAdams, Harley H.
dc.contributor.authorShapiro, Lucy
dc.contributor.authorDekker, Job
dc.contributor.authorChurch, George M.
dc.date2022-08-11T08:10:15.000
dc.date.accessioned2022-08-23T17:01:13Z
dc.date.available2022-08-23T17:01:13Z
dc.date.issued2011-10-25
dc.date.submitted2011-11-08
dc.identifier.citationMol Cell. 2011 Oct 21;44(2):252-64. <a href="http://dx.doi.org/10.1016/j.molcel.2011.09.010">Link to article on publisher's site</a>
dc.identifier.issn1097-2765 (Linking)
dc.identifier.doi10.1016/j.molcel.2011.09.010
dc.identifier.pmid22017872
dc.identifier.urihttp://hdl.handle.net/20.500.14038/43960
dc.description.abstractWe have determined the three-dimensional (3D) architecture of the Caulobacter crescentus genome by combining genome-wide chromatin interaction detection, live-cell imaging, and computational modeling. Using chromosome conformation capture carbon copy (5C), we derive approximately 13 kb resolution 3D models of the Caulobacter genome. The resulting models illustrate that the genome is ellipsoidal with periodically arranged arms. The parS sites, a pair of short contiguous sequence elements known to be involved in chromosome segregation, are positioned at one pole, where they anchor the chromosome to the cell and contribute to the formation of a compact chromatin conformation. Repositioning these elements resulted in rotations of the chromosome that changed the subcellular positions of most genes. Such rotations did not lead to large-scale changes in gene expression, indicating that genome folding does not strongly affect gene regulation. Collectively, our data suggest that genome folding is globally dictated by the parS sites and chromosome segregation.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=22017872&dopt=Abstract">Link to Article in PubMed</a>
dc.relation.urlhttp://dx.doi.org/10.1016/j.molcel.2011.09.010
dc.subjectCaulobacter crescentus
dc.subjectGenome, Bacterial
dc.subjectChromosomes, Bacterial
dc.subjectImaging, Three-Dimensional
dc.subjectGenetics and Genomics
dc.titleThe three-dimensional architecture of a bacterial genome and its alteration by genetic perturbation
dc.typeJournal Article
dc.source.journaltitleMolecular cell
dc.source.volume44
dc.source.issue2
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/pgfe_pp/171
dc.identifier.contextkey2336483
html.description.abstract<p>We have determined the three-dimensional (3D) architecture of the Caulobacter crescentus genome by combining genome-wide chromatin interaction detection, live-cell imaging, and computational modeling. Using chromosome conformation capture carbon copy (5C), we derive approximately 13 kb resolution 3D models of the Caulobacter genome. The resulting models illustrate that the genome is ellipsoidal with periodically arranged arms. The parS sites, a pair of short contiguous sequence elements known to be involved in chromosome segregation, are positioned at one pole, where they anchor the chromosome to the cell and contribute to the formation of a compact chromatin conformation. Repositioning these elements resulted in rotations of the chromosome that changed the subcellular positions of most genes. Such rotations did not lead to large-scale changes in gene expression, indicating that genome folding does not strongly affect gene regulation. Collectively, our data suggest that genome folding is globally dictated by the parS sites and chromosome segregation.</p>
dc.identifier.submissionpathpgfe_pp/171
dc.contributor.departmentProgram in Systems Biology
dc.contributor.departmentDepartment of Biochemistry and Molecular Pharmacology
dc.contributor.departmentProgram in Gene Function and Expression
dc.source.pages252-64


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