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dc.contributor.authorDong, Guogang
dc.contributor.authorYang, Qiong
dc.contributor.authorWang, Qiang
dc.contributor.authorKim, Yong-Ick
dc.contributor.authorWood, Thammajun L.
dc.contributor.authorOsteryoung, Katherine W.
dc.contributor.authorvan Oudenaarden, Alexander
dc.contributor.authorGolden, Susan S.
dc.date.accessioned2013-01-30T19:47:15Z
dc.date.available2013-01-30T19:47:15Z
dc.date.issued2010-02
dc.identifier.issn1097-4172
dc.identifier.issn0092-8674
dc.identifier.urihttp://hdl.handle.net/1721.1/76679
dc.descriptionavailable in PMC 2011 February 1.en_US
dc.description.abstractA circadian clock coordinates physiology and behavior in diverse groups of living organisms. Another major cyclic cellular event, the cell cycle, is regulated by the circadian clock in the few cases where linkage of these cycles has been studied. In the cyanobacterium Synechococcus elongatus, the circadian clock gates cell division by an unknown mechanism. Using timelapse microscopy, we confirm the gating of cell division in the wild-type and demonstrate the regulation of cytokinesis by key clock components. Specifically, a state of the oscillator protein KaiC that is associated with elevated ATPase activity closes the gate by acting through a known clock output pathway to inhibit FtsZ ring formation at the division site. An activity that stimulates KaiC phosphorylation independently of the KaiA protein was also uncovered. We propose a model that separates the functions of KaiC ATPase and phosphorylation in cell division gating and other circadian behaviors.en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (NIH (R01 GM62419))en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (grant P01 NS39546)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (grant R01 GM068957)en_US
dc.description.sponsorshipUnited States. American Recovery and Reinvestment Act of 2009en_US
dc.description.sponsorshipNational Science Foundation (U.S.) (PHY-0548484)en_US
dc.description.sponsorshipUnited States. Dept. of Energy (DE-FG-02-06ER15808)en_US
dc.language.isoen_US
dc.publisherElsevier B.V.en_US
dc.relation.isversionofhttp://dx.doi.org/10.1016/j.cell.2009.12.042en_US
dc.rightsCreative Commons Attribution-Noncommercial-Share Alike 3.0en_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/3.0/en_US
dc.sourcePMCen_US
dc.titleElevated ATPase Activity of KaiC Constitutes a Circadian Checkpoint of Cell Division in Synechococcus elongatusen_US
dc.typeArticleen_US
dc.identifier.citationDong, Guogang et al. “Elevated ATPase Activity of KaiC Applies a Circadian Checkpoint on Cell Division in Synechococcus Elongatus.” Cell 140.4 (2010): 529–539. Web.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Mathematicsen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Physicsen_US
dc.contributor.mitauthorvan Oudenaarden, Alexander
dc.relation.journalCellen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsDong, Guogang; Yang, Qiong; Wang, Qiang; Kim, Yong-Ick; Wood, Thammajun L.; Osteryoung, Katherine W.; van Oudenaarden, Alexander; Golden, Susan S.en
mit.licenseOPEN_ACCESS_POLICYen_US
mit.metadata.statusComplete


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