Regulation of mitotic progression by the spindle assembly checkpoint

被引:44
作者
Lischetti, Tiziana [1 ]
Nilsson, Jakob [1 ]
机构
[1] Univ Copenhagen, Novo Nordisk Fdn, Fac Hlth & Med Sci, Ctr Prot Res, Copenhagen, Denmark
关键词
APC/C; Kinetochore; Mitosis; SAC;
D O I
10.4161/23723548.2014.970484
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Equal segregation of sister chromatids during mitosis requires that pairs of kinetochores establish proper attachment to microtubules emanating from opposite poles of the mitotic spindle. The spindle assembly checkpoint (SAC) protects against errors in segregation by delaying sister separation in response to improper kinetochore-microtubule interactions, and certain checkpoint proteins help to establish proper attachments. Anaphase entry is inhibited by the checkpoint through assembly of the mitotic checkpoint complex (MCC) composed of the 2 checkpoint proteins, Mad2 and BubR1, bound to Cdc20. The outer kinetochore acts as a catalyst for MCC production through the recruitment and proper positioning of checkpoint proteins and recently there has been remarkable progress in understanding how this is achieved. Here, we highlight recent advances in our understanding of kinetochore-checkpoint protein interactions and inhibition of the anaphase promoting complex by the MCC.
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页数:11
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