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dc.contributor.authorHung, Hui-Fang
dc.contributor.authorHehnly, Heidi
dc.contributor.authorDoxsey, Stephen J
dc.date2022-08-11T08:08:56.000
dc.date.accessioned2022-08-23T16:12:59Z
dc.date.available2022-08-23T16:12:59Z
dc.date.issued2015-09-12
dc.date.submitted2017-09-13
dc.identifier.citation<p>Methods Cell Biol. 2015;130:47-58. doi: 10.1016/bs.mcb.2015.03.024. Epub 2015 Jun 11. <a href="https://doi.org/10.1016/bs.mcb.2015.03.024">Link to article on publisher's site</a></p>
dc.identifier.issn0091-679X (Linking)
dc.identifier.doi10.1016/bs.mcb.2015.03.024
dc.identifier.pmid26360027
dc.identifier.urihttp://hdl.handle.net/20.500.14038/33512
dc.description.abstractFor some time, it has been known that recycling endosomes (REs) are organized in a nebulous "pericentrosomal" region in interphase cells. However, the collective use of previously developed methods, including centrosome isolation, live cell imaging, and electron microscopy, suggested that there is much more going on between the centrosome and the RE than previously imagined. By exploiting these approaches, we uncovered novel roles of the centrosome in RE function and, conversely, novel roles for REs in centrosome function. We first found that REs dynamically localized to the centrosome throughout the cell cycle. More specifically, we found that REs interacted with appendages of the older centriole in interphase cells to control endosome recycling, and this interaction was governed by RE-machinery including the small GTPase Rab11. We next determined that REs carry centrosome proteins to spindle poles as part of the "centrosome maturation" process. Here we discuss the methods used and materials needed to complete these types of studies.
dc.language.isoen_US
dc.relation<p><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=26360027&dopt=Abstract">Link to Article in PubMed</a></p>
dc.relation.urlhttps://doi.org/10.1016/bs.mcb.2015.03.024
dc.subjectAppendages
dc.subjectCenexin
dc.subjectCentriolin
dc.subjectCentrosome
dc.subjectCentrosome isolation
dc.subjectEvi5
dc.subjectFip3
dc.subjectMitosis
dc.subjectMother centriole
dc.subjectRab11
dc.subjectRab8
dc.subjectRecycling endosome
dc.subjectSpindle pole
dc.subjectCell Biology
dc.titleMethods to analyze novel liaisons between endosomes and centrosomes
dc.typeJournal Article
dc.source.journaltitleMethods in cell biology
dc.source.volume130
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/gsbs_sp/2037
dc.identifier.contextkey10740196
html.description.abstract<p>For some time, it has been known that recycling endosomes (REs) are organized in a nebulous "pericentrosomal" region in interphase cells. However, the collective use of previously developed methods, including centrosome isolation, live cell imaging, and electron microscopy, suggested that there is much more going on between the centrosome and the RE than previously imagined. By exploiting these approaches, we uncovered novel roles of the centrosome in RE function and, conversely, novel roles for REs in centrosome function. We first found that REs dynamically localized to the centrosome throughout the cell cycle. More specifically, we found that REs interacted with appendages of the older centriole in interphase cells to control endosome recycling, and this interaction was governed by RE-machinery including the small GTPase Rab11. We next determined that REs carry centrosome proteins to spindle poles as part of the "centrosome maturation" process. Here we discuss the methods used and materials needed to complete these types of studies.</p>
dc.identifier.submissionpathgsbs_sp/2037
dc.contributor.departmentProgram in Molecular Medicine
dc.source.pages47-58
dc.contributor.studentHui-Fang Hung


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