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dc.contributor.authorRay, Samriddha
dc.contributor.authorKume, Kazunori
dc.contributor.authorGupta, Sneha
dc.contributor.authorGe, Wanzhong
dc.contributor.authorBalasubramanian, Mohan
dc.contributor.authorHirata, Dai
dc.contributor.authorMcCollum, Dannel
dc.date2022-08-11T08:08:55.000
dc.date.accessioned2022-08-23T16:12:06Z
dc.date.available2022-08-23T16:12:06Z
dc.date.issued2010-09-06
dc.date.submitted2014-03-18
dc.identifier.citationRay S, Kume K, Gupta S, Ge W, alasubramanian M, Hirata D, McCollum D. The mitosis-to-interphase transition is coordinated by cross talk between the SIN and MOR pathways in Schizosaccharomyces pombe. J Cell Biol. 2010 Sep 6;190(5):793-805. doi: 10.1083/jcb.201002055. <a href="http://dx.doi.org/10.1083/jcb.201002055">Link to article on publisher's site</a>
dc.identifier.issn0021-9525 (Linking)
dc.identifier.doi10.1083/jcb.201002055
dc.identifier.pmid20805322
dc.identifier.urihttp://hdl.handle.net/20.500.14038/33324
dc.description.abstractThe mechanisms that regulate cytoskeletal remodeling during the transition between mitosis and interphase are poorly understood. In fission yeast the MOR pathway promotes actin polarization to cell tips in interphase, whereas the SIN signaling pathway drives actomyosin ring assembly and cytokinesis. We show that the SIN inhibits MOR signaling in mitosis by interfering with Nak1 kinase-mediated activation of the most downstream MOR component, the NDR family kinase Orb6. Inactivation of the MOR may be a key function of the SIN because attenuation of MOR signaling rescued the cytokinetic defects of SIN mutants and allowed weak SIN signaling to trigger ectopic cytokinesis. Furthermore, failure to inhibit the MOR is toxic when the cell division apparatus is compromised. Together, our results reveal a mutually antagonistic relationship between the SIN and MOR pathways, which is important for completion of cytokinesis and coordination of cytoskeletal remodeling at the mitosis-to-interphase transition.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=20805322&dopt=Abstract">Link to Article in PubMed</a>
dc.rights<p>This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described athttp://creativecommons.org/licenses/by-nc-sa/3.0/).</p>
dc.subjectActins; Cell Division; Cytokinesis; Green Fluorescent Proteins; Interphase; *Mitosis; Recombinant Fusion Proteins; *Schizosaccharomyces; Schizosaccharomyces pombe Proteins; Signal Transduction
dc.subjectCell Biology
dc.subjectCellular and Molecular Physiology
dc.titleThe mitosis-to-interphase transition is coordinated by cross talk between the SIN and MOR pathways in Schizosaccharomyces pombe
dc.typeJournal Article
dc.source.journaltitleThe Journal of cell biology
dc.source.volume190
dc.source.issue5
dc.identifier.legacyfulltexthttps://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=2871&amp;context=gsbs_sp&amp;unstamped=1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/gsbs_sp/1851
dc.identifier.contextkey5351549
refterms.dateFOA2022-08-23T16:12:06Z
html.description.abstract<p>The mechanisms that regulate cytoskeletal remodeling during the transition between mitosis and interphase are poorly understood. In fission yeast the MOR pathway promotes actin polarization to cell tips in interphase, whereas the SIN signaling pathway drives actomyosin ring assembly and cytokinesis. We show that the SIN inhibits MOR signaling in mitosis by interfering with Nak1 kinase-mediated activation of the most downstream MOR component, the NDR family kinase Orb6. Inactivation of the MOR may be a key function of the SIN because attenuation of MOR signaling rescued the cytokinetic defects of SIN mutants and allowed weak SIN signaling to trigger ectopic cytokinesis. Furthermore, failure to inhibit the MOR is toxic when the cell division apparatus is compromised. Together, our results reveal a mutually antagonistic relationship between the SIN and MOR pathways, which is important for completion of cytokinesis and coordination of cytoskeletal remodeling at the mitosis-to-interphase transition.</p>
dc.identifier.submissionpathgsbs_sp/1851
dc.contributor.departmentDepartment of Molecular Genetics and Microbiology
dc.source.pages793-805
dc.contributor.studentSamriddha Ray; Sneha Gupta


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