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dc.contributor.authorLa Terra, Sabrina
dc.contributor.authorEnglish, Christopher N.
dc.contributor.authorHergert, Polla J.
dc.contributor.authorMcEwen, Bruce F.
dc.contributor.authorSluder, Greenfield
dc.contributor.authorKhodjakov, Alexey
dc.date2022-08-11T08:10:53.000
dc.date.accessioned2022-08-23T17:23:46Z
dc.date.available2022-08-23T17:23:46Z
dc.date.issued2005-03-02
dc.date.submitted2011-03-24
dc.identifier.citationJ Cell Biol. 2005 Feb 28;168(5):713-22. <a href="http://dx.doi.org/10.1083/jcb.200411126">Link to article on publisher's site</a>
dc.identifier.issn0021-9525 (Linking)
dc.identifier.doi10.1083/jcb.200411126
dc.identifier.pmid15738265
dc.identifier.urihttp://hdl.handle.net/20.500.14038/49036
dc.description.abstractIt has been reported that nontransformed mammalian cells become arrested during G1 in the absence of centrioles (Hinchcliffe, E., F. Miller, M. Cham, A. Khodjakov, and G. Sluder. 2001. Science. 291:1547-1550). Here, we show that removal of resident centrioles (by laser ablation or needle microsurgery) does not impede cell cycle progression in HeLa cells. HeLa cells born without centrosomes, later, assemble a variable number of centrioles de novo. Centriole assembly begins with the formation of small centrin aggregates that appear during the S phase. These, initially amorphous "precentrioles" become morphologically recognizable centrioles before mitosis. De novo-assembled centrioles mature (i.e., gain abilities to organize microtubules and replicate) in the next cell cycle. This maturation is not simply a time-dependent phenomenon, because de novo-formed centrioles do not mature if they are assembled in S phase-arrested cells. By selectively ablating only one centriole at a time, we find that the presence of a single centriole inhibits the assembly of additional centrioles, indicating that centrioles have an activity that suppresses the de novo pathway.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=15738265&dopt=Abstract">Link to Article in PubMed</a>
dc.subjectCell Cycle
dc.subjectCentrioles
dc.subjectGenes, Reporter
dc.subjectHela Cells
dc.subjectHumans
dc.subjectS Phase
dc.subjectCell Biology
dc.titleThe de novo centriole assembly pathway in HeLa cells: cell cycle progression and centriole assembly/maturation
dc.typeJournal Article
dc.source.journaltitleThe Journal of cell biology
dc.source.volume168
dc.source.issue5
dc.identifier.legacyfulltexthttps://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=1008&amp;context=sluder&amp;unstamped=1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/sluder/9
dc.identifier.contextkey1898090
refterms.dateFOA2022-08-23T17:23:46Z
html.description.abstract<p>It has been reported that nontransformed mammalian cells become arrested during G1 in the absence of centrioles (Hinchcliffe, E., F. Miller, M. Cham, A. Khodjakov, and G. Sluder. 2001. Science. 291:1547-1550). Here, we show that removal of resident centrioles (by laser ablation or needle microsurgery) does not impede cell cycle progression in HeLa cells. HeLa cells born without centrosomes, later, assemble a variable number of centrioles de novo. Centriole assembly begins with the formation of small centrin aggregates that appear during the S phase. These, initially amorphous "precentrioles" become morphologically recognizable centrioles before mitosis. De novo-assembled centrioles mature (i.e., gain abilities to organize microtubules and replicate) in the next cell cycle. This maturation is not simply a time-dependent phenomenon, because de novo-formed centrioles do not mature if they are assembled in S phase-arrested cells. By selectively ablating only one centriole at a time, we find that the presence of a single centriole inhibits the assembly of additional centrioles, indicating that centrioles have an activity that suppresses the de novo pathway.</p>
dc.identifier.submissionpathsluder/9
dc.contributor.departmentDepartment of Cell Biology
dc.source.pages713-22


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