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pubmed-article:20705812pubmed:dateCreated2010-10-8lld:pubmed
pubmed-article:20705812pubmed:abstractTextAurora B is a component of the chromosomal passenger complex (CPC) required for correct spindle-kinetochore attachments during chromosome segregation and for cytokinesis. The chromatin factors that recruit the CPC to centromeres are unknown, however. Here we show that phosphorylation of histone H3 threonine 3 (H3T3ph) by Haspin is necessary for CPC accumulation at centromeres and that the CPC subunit Survivin binds directly to H3T3ph. A nonbinding Survivin-D70A/D71A mutant does not support centromeric CPC concentration, and both Haspin depletion and Survivin-D70A/D71A mutation diminish centromere localization of the kinesin MCAK and the mitotic checkpoint response to taxol. Survivin-D70A/D71A mutation and microinjection of H3T3ph-specific antibody both compromise centromeric Aurora B functions but do not prevent cytokinesis. Therefore, H3T3ph generated by Haspin positions the CPC at centromeres to regulate selected targets of Aurora B during mitosis.lld:pubmed
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pubmed-article:20705812pubmed:authorpubmed-author:OshJ AJAlld:pubmed
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pubmed-article:20705812pubmed:authorpubmed-author:GorbskyGary...lld:pubmed
pubmed-article:20705812pubmed:authorpubmed-author:HigginsJonath...lld:pubmed
pubmed-article:20705812pubmed:authorpubmed-author:DaumJohn RJRlld:pubmed
pubmed-article:20705812pubmed:authorpubmed-author:WangFangweiFlld:pubmed
pubmed-article:20705812pubmed:authorpubmed-author:Niedzialkowsk...lld:pubmed
pubmed-article:20705812pubmed:authorpubmed-author:BanerjeeBudha...lld:pubmed
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