Correcting improper chromosome-spindle attachments during cell division

被引:352
作者
Lampson, MA
Renduchitala, K
Khodjakov, A
Kapoor, TM
机构
[1] Rockefeller Univ, Lab Chem & Cell Biol, New York, NY 10021 USA
[2] New York State Dept Hlth, Wadsworth Ctr Labs & Res, Div Mol Med, Albany, NY 12201 USA
关键词
D O I
10.1038/ncb1102
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
For accurate segregation of chromosomes during cell division, microtubule fibres must attach sister kinetochores to opposite poles of the mitotic spindle (bi-orientation). Aurora kinases are linked to oncogenesis(1) and have been implicated in the regulation of chromosome-microtubule attachments(2). Although loss of Aurora kinase activity causes an accumulation of mal-orientated chromosomes in dividing cells(3,4), it is not known how the active kinase corrects improper chromosome attachments. The use of reversible small-molecule inhibitors allows activation of protein function in living vertebrate cells with temporal control. Here we show that by removal of small-molecule inhibitors, controlled activation of Aurora kinase during mitosis can correct chromosome attachment errors by selective disassembly of kinetochore-microtubule fibres, rather than by alternative mechanisms involving initial release of microtubules from either kinetochores or spindle poles(5-7). Observation of chromosomes and microtubule dynamics with real-time high-resolution microscopy showed that mal-orientated, but not bi-orientated, chromosomes move to the spindle pole as both kinetochore-microtubule fibres shorten, followed by alignment at the metaphase plate. Our results provide direct evidence for a mechanism required for the maintenance of genome integrity during cell division.
引用
收藏
页码:232 / 237
页数:6
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