EB1 enables spindle microtubules to regulate centromeric recruitment of Aurora B

被引:44
作者
Banerjee, Budhaditya [1 ]
Kestner, Cortney A. [1 ]
Stukenberg, P. Todd [1 ]
机构
[1] Univ Virginia, Dept Biochem & Mol Genet, Charlottesville, VA 22908 USA
基金
美国国家卫生研究院;
关键词
CHROMOSOMAL PASSENGER COMPLEX; PHOSPHORYLATED HISTONE H3; SMALL-MOLECULE INHIBITOR; INNER CENTROMERE; STRUCTURAL BASIS; KINASE-ACTIVITY; PROTEIN INCENP; BUDDING YEAST; ACTIVATION; CHECKPOINT;
D O I
10.1083/jcb.201307119
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The Aurora B kinase coordinates kinetochore-microtubule attachments with spindle checkpoint signaling on each mitotic chromosome. We find that EB1, a microtubule plus end-tracking protein, is required to enrich Aurora B at inner centromeres in a microtubule-dependent manner. This regulates phosphorylation of both kinetochore and chromatin substrates. EB1 regulates the histone phosphorylation marks (histone H2A phospho-Thr120 and histone H3 phospho-Thr3) that localize Aurora B. The chromosomal passenger complex containing Aurora B can be found on a subset of spindle microtubules that exist near prometaphase kinetochores, known as preformed K-fibers (kinetochore fibers). Our data suggest that EB1 enables the spindle microtubules to regulate the phosphorylation of kinetochores through recruitment of the Aurora B kinase.
引用
收藏
页码:947 / 963
页数:17
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