Sensing centromere tension: Aurora B and the regulation of kinetochore function

被引:296
作者
Lampson, Michael A. [1 ]
Cheeseman, Iain M. [2 ,3 ]
机构
[1] Univ Penn, Dept Biol, Philadelphia, PA 19104 USA
[2] MIT, Dept Biol, Cambridge, MA 02142 USA
[3] MIT, Whitehead Inst Biomed Res, Cambridge, MA 02142 USA
基金
美国国家卫生研究院;
关键词
SPINDLE ASSEMBLY CHECKPOINT; PROTEIN PHOSPHATASE 1; MICROTUBULE-ATTACHMENT; INNER CENTROMERE; CHROMOSOME SEGREGATION; BUDDING YEAST; HISTONE H3; ORIENTED CHROMOSOMES; MITOTIC PROGRESSION; SURVIVIN FUNCTION;
D O I
10.1016/j.tcb.2010.10.007
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Maintaining genome integrity during cell division requires regulated interactions between chromosomes and spindle microtubules. To ensure that daughter cells inherit the correct chromosomes, the sister kinetochores must attach to opposite spindle poles. Tension across the centromere stabilizes correct attachments, whereas phosphorylation of kinetochore substrates by the conserved Ipl1/Aurora B kinase selectively eliminates incorrect attachments. Here, we review our current understanding of how mechanical forces acting on the kinetochore are linked to biochemical changes to control chromosome segregation. We discuss models for tension sensing and regulation of kinetochore function downstream of Aurora B, and mechanisms that specify Aurora B localization to the inner centromere and determine its interactions with substrates at distinct locations.
引用
收藏
页码:133 / 140
页数:8
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