Aurora A kinase activity is required to maintain an active spindle assembly checkpoint during prometaphase

被引:24
|
作者
Courtheoux, Thibault [1 ]
Diallo, Alghassimou [1 ]
Damodaran, Arun Prasath [1 ]
Reboutier, David [1 ]
Watrin, Erwan [1 ]
Prigent, Claude [1 ]
机构
[1] Univ Rennes, CNRS, IGDR, UMR 6290,Equipe Labellisee Ligue Canc 2014 2016, F-35000 Rennes, France
关键词
Aurora A; Spindle; Checkpoint; SMALL-MOLECULE INHIBITOR; A-KINASE; CHROMATIN CONDENSATION; CENTROSOME MATURATION; CELL-DIVISION; PHOSPHORYLATION; PROTEIN; CANCER; MCAK; AMPLIFICATION;
D O I
10.1242/jcs.191353
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
During the prometaphase stage of mitosis, the cell builds a bipolar spindle of microtubules that mechanically segregates sister chromatids between two daughter cells in anaphase. The spindle assembly checkpoint (SAC) is a quality control mechanism that monitors proper attachment of microtubules to chromosome kinetochores during prometaphase. Segregation occurs only when each chromosome is bi-oriented with each kinetochore pair attached to microtubules emanating from opposite spindle poles. Overexpression of the protein kinase Aurora A is a feature of various cancers and is thought to enable tumour cells to bypass the SAC, leading to aneuploidy. Here, we took advantage of a chemical and chemical-genetic approach to specifically inhibit Aurora A kinase activity in late prometaphase. We observed that a loss of Aurora A activity directly affects SAC function, that Aurora A is essential for maintaining the checkpoint protein Mad2 on unattached kinetochores and that inhibition of Aurora A leads to loss of the SAC, even in the presence of nocodazole or Taxol. This is a new finding that should affect the way Aurora A inhibitors are used in cancer treatments.
引用
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页数:12
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