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dc.contributor.authorKotýnková, Kristýna
dc.contributor.authorSu, Kuan-Chung
dc.contributor.authorWest, Stephen C.
dc.contributor.authorPetronczki, Mark
dc.date.accessioned2017-03-15T15:29:25Z
dc.date.available2017-03-15T15:29:25Z
dc.date.issued2016-12
dc.identifier.issn22111247
dc.identifier.urihttp://hdl.handle.net/1721.1/107414
dc.description.abstractCytokinesis, the final step of cell division, begins with the formation of a cleavage furrow. How the mitotic spindle specifies the furrow at the equator in animal cells remains unknown. Current models propose that the concentration of the RhoGEF ECT2 at the spindle midzone and the equatorial plasma membrane directs furrow formation. Using chemical genetic and optogenetic tools, we demonstrate that the association of ECT2 with the plasma membrane during anaphase is required and sufficient for cytokinesis. Local membrane targeting of ECT2 leads to unilateral furrowing, highlighting the importance of local ECT2 activity. ECT2 mutations that prevent centralspindlin binding compromise concentration of ECT2 at the midzone and equatorial membrane but sustain cytokinesis. While the association of ECT2 with the plasma membrane is essential for cytokinesis, our data suggest that ECT2 recruitment to the spindle midzone is insufficient to account for equatorial furrowing and may act redundantly with yet-uncharacterized signals.en_US
dc.description.sponsorshipCancer Research UKen_US
dc.language.isoen_US
dc.publisherElsevieren_US
dc.relation.isversionofhttp://dx.doi.org/10.1016/j.celrep.2016.11.029en_US
dc.rightsCreative Commons Attribution 4.0 International Licenseen_US
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en_US
dc.sourceElsevieren_US
dc.titlePlasma Membrane Association but Not Midzone Recruitment of RhoGEF ECT2 Is Essential for Cytokinesisen_US
dc.typeArticleen_US
dc.identifier.citationKotýnková, Kristýna, Kuan-Chung Su, Stephen C. West, and Mark Petronczki. “Plasma Membrane Association but Not Midzone Recruitment of RhoGEF ECT2 Is Essential for Cytokinesis.” Cell Reports 17, no. 10 (December 2016): 2672–2686.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biologyen_US
dc.contributor.departmentWhitehead Institute for Biomedical Researchen_US
dc.contributor.mitauthorSu, Kuan-Chung
dc.relation.journalCell Reportsen_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.orderedauthorsKotýnková, Kristýna; Su, Kuan-Chung; West, Stephen C.; Petronczki, Marken_US
dspace.embargo.termsNen_US
mit.licensePUBLISHER_CCen_US


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