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dc.contributor.authorMurata-Hori, Maki
dc.contributor.authorSluder, Greenfield
dc.contributor.authorWang, Yu-Li
dc.date2022-08-11T08:09:47.000
dc.date.accessioned2022-08-23T16:43:34Z
dc.date.available2022-08-23T16:43:34Z
dc.date.issued2004-12-25
dc.date.submitted2008-04-14
dc.identifier.citationBMC Cell Biol. 2004 Dec 23;5(1):49. <a href="http://dx.doi.org/10.1186/1471-2121-5-49">Link to article on publisher's site</a>
dc.identifier.issn1471-2121 (Electronic)
dc.identifier.doi10.1186/1471-2121-5-49
dc.identifier.pmid15617574
dc.identifier.urihttp://hdl.handle.net/20.500.14038/40319
dc.description.abstractBACKGROUND: A number of proteins accumulate in the spindle midzone and midbody of dividing animal cells. Besides proteins essential for cytokinesis, there are also components essential for interphase functions, suggesting that the spindle midzone and/or midbody may play a role in regulating the following cell cycle. RESULTS: We microsurgically severed NRK epithelial cells during anaphase or telophase, such that the spindle midzone/midbody was associated with only one of the daughter cells. Time-lapse recording of cells severed during early anaphase indicated that the cell with midzone underwent cytokinesis-like cortical contractions and progressed normally through the interphase, whereas the cell without midzone showed no cortical contraction and an arrest or substantial delay in the progression of interphase. Similar microsurgery during telophase showed a normal progression of interphase for both daughter cells with or without the midbody. Microsurgery of anaphase cells treated with cytochalasin D or nocodazole indicated that interphase progression was independent of cortical ingression but dependent on microtubules. CONCLUSIONS: We conclude that the mitotic spindle is involved in not only the separation of chromosomes but also the regulation of cell cycle. The process may involve activation of components in the spindle midzone that are required for the cell cycle, and/or degradation of components that are required for cytokinesis but may interfere with the cell cycle.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=15617574&dopt=Abstract">Link to article in PubMed</a>
dc.subject*Anaphase
dc.subjectAnimals
dc.subject*Cell Cycle
dc.subjectCell Line
dc.subjectEpithelial Cells
dc.subjectInterphase
dc.subjectMicrosurgery
dc.subjectMitotic Spindle Apparatus
dc.subjectRats
dc.subjectCell Biology
dc.subjectLife Sciences
dc.subjectMedicine and Health Sciences
dc.titleRegulation of cell cycle by the anaphase spindle midzone
dc.typeJournal Article
dc.source.journaltitleBMC cell biology
dc.source.volume5
dc.source.issue1
dc.identifier.legacyfulltexthttps://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=1311&amp;context=oapubs&amp;unstamped=1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/oapubs/312
dc.identifier.contextkey489650
refterms.dateFOA2022-08-23T16:43:34Z
html.description.abstract<p>BACKGROUND: A number of proteins accumulate in the spindle midzone and midbody of dividing animal cells. Besides proteins essential for cytokinesis, there are also components essential for interphase functions, suggesting that the spindle midzone and/or midbody may play a role in regulating the following cell cycle.</p> <p>RESULTS: We microsurgically severed NRK epithelial cells during anaphase or telophase, such that the spindle midzone/midbody was associated with only one of the daughter cells. Time-lapse recording of cells severed during early anaphase indicated that the cell with midzone underwent cytokinesis-like cortical contractions and progressed normally through the interphase, whereas the cell without midzone showed no cortical contraction and an arrest or substantial delay in the progression of interphase. Similar microsurgery during telophase showed a normal progression of interphase for both daughter cells with or without the midbody. Microsurgery of anaphase cells treated with cytochalasin D or nocodazole indicated that interphase progression was independent of cortical ingression but dependent on microtubules.</p> <p>CONCLUSIONS: We conclude that the mitotic spindle is involved in not only the separation of chromosomes but also the regulation of cell cycle. The process may involve activation of components in the spindle midzone that are required for the cell cycle, and/or degradation of components that are required for cytokinesis but may interfere with the cell cycle.</p>
dc.identifier.submissionpathoapubs/312
dc.contributor.departmentDepartment of Cell Biology
dc.contributor.departmentDepartment of Physiology
dc.source.pages49


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