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dc.contributor.authorChan, Leon Y.
dc.contributor.authorAmon, Angelika B
dc.date.accessioned2013-12-10T21:31:13Z
dc.date.available2013-12-10T21:31:13Z
dc.date.issued2010-08
dc.identifier.issn10972765
dc.identifier.urihttp://hdl.handle.net/1721.1/82909
dc.description.abstractHow spatial information is translated into a chemical signal is a fundamental problem in all organisms. The spindle position checkpoint is a prime example of this problem. This checkpoint senses spindle position and, in budding yeast, inhibits the mitotic exit network (MEN), a signaling pathway that promotes exit from mitosis. We find that spindle position is sensed by a system composed of MEN-inhibitory and -activating zones and a sensor that moves between them. The MEN inhibitory zone is located in the mother cell, the MEN-activating zone in the bud, and the spindle pole body (SPB), where the components of the MEN reside, functions as the sensor. Only when an SPB escapes the MEN inhibitor Kin4 in the mother cell and moves into the bud where the MEN activator Lte1 resides can exit from mitosis occur. In this manner, spatial information is sensed and translated into a chemical signal.en_US
dc.description.sponsorshipNational Science Foundation (U.S.) (NSF Predoctoral Fellowship)en_US
dc.description.sponsorshipHoward Hughes Medical Institute (Investigator)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (GM056800)en_US
dc.language.isoen_US
dc.publisherElsevier B.V.en_US
dc.relation.isversionofhttp://dx.doi.org/10.1016/j.molcel.2010.07.032en_US
dc.rightsArticle is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.en_US
dc.sourceElsevier Open Archiveen_US
dc.titleSpindle Position Is Coordinated with Cell-Cycle Progression through Establishment of Mitotic Exit-Activating and -Inhibitory Zonesen_US
dc.typeArticleen_US
dc.identifier.citationChan, Leon Y., and Angelika Amon. “Spindle Position Is Coordinated with Cell-Cycle Progression through Establishment of Mitotic Exit-Activating and -Inhibitory Zones.” Molecular Cell 39, no. 3 (August 2010): 444-454.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biologyen_US
dc.contributor.departmentKoch Institute for Integrative Cancer Research at MITen_US
dc.contributor.mitauthorAmon, Angelika B.en_US
dc.contributor.mitauthorChan, Leon Y.en_US
dc.relation.journalMolecular Cellen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsChan, Leon Y.; Amon, Angelikaen_US
dc.identifier.orcidhttps://orcid.org/0000-0001-9837-0314
mit.licensePUBLISHER_POLICYen_US
mit.metadata.statusComplete


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