Bub1 and CENP-U redundantly recruit Plk1 to stabilize kinetochore-microtubule attachments and ensure accurate chromosome segregation

被引:25
作者
Chen, Qinfu [1 ,2 ]
Zhang, Miao [2 ]
Pan, Xuan [2 ]
Yuan, Xueying [2 ]
Zhou, Linli [2 ]
Yan, Lu [2 ]
Zeng, Ling-Hui [1 ]
Xu, Junfen [3 ]
Yang, Bing [2 ]
Zhang, Long [2 ]
Huang, Jun [2 ]
Lu, Weiguo [3 ,4 ]
Fukagawa, Tatsuo [5 ]
Wang, Fangwei [2 ,3 ,4 ]
Yan, Haiyan [1 ]
机构
[1] Zhejiang Univ City Coll, Dept Pharmacol, Hangzhou 310015, Peoples R China
[2] Zhejiang Univ, Life Sci Inst, Key Lab Canc Mol Cell Biol Zhejiang Prov, MOE Key Lab Biosyst Homeostasis & Protect, Hangzhou 310058, Peoples R China
[3] Zhejiang Univ, Womens Hosp, Dept Gynecol Oncol, Sch Med, Hangzhou 310006, Peoples R China
[4] Zhejiang Univ, Canc Ctr, Hangzhou 310058, Peoples R China
[5] Osaka Univ, Grad Sch Frontier Biosci, Suita, Osaka 5650871, Japan
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
AURORA B KINASE; PROTECTS CENTROMERIC COHESION; SMALL-MOLECULE INHIBITOR; THR-3; PHOSPHORYLATION; ESSENTIAL GENES; LOCALIZATION; CHECKPOINT; COMPLEX; HASPIN; BINDING;
D O I
10.1016/j.celrep.2021.109740
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Bub1 is required for the kinetochore/centromere localization of two essential mitotic kinases Plk1 and Aurora B. Surprisingly, stable depletion of Bub1 by similar to 95% in human cells marginally affects whole chromosome segregation fidelity. We show that CENP-U, which is recruited to kinetochores by the CENP-P and CENP-Q subunits of the CENP-O complex, is required to prevent chromosome mis-segregation in Bub1-depleted cells. Mechanistically, Bub1 and CENP-U redundantly recruit Plk1 to kinetochores to stabilize kinetochoremicrotubule attachments, thereby ensuring accurate chromosome segregation. Furthermore, unlike its budding yeast homolog, the CENP-O complex does not regulate centromeric localization of Aurora B. Consistently, depletion of Bub1 or CENP-U sensitizes cells to the inhibition of Plk1 but not Aurora B kinase activity. Taken together, our findings provide mechanistic insight into the regulation of kinetochore function, which may have implications for targeted treatment of cancer cells with mutations perturbing kinetochore recruitment of Plk1 by Bub1 or the CENP-O complex.
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页数:24
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