To cell cycle, swing the APC/C

被引:113
作者
van Leuken, Renske [1 ,2 ]
Clijsters, Linda [1 ]
Wolthuis, Rob [1 ]
机构
[1] Netherlands Canc Inst, Div Mol Biol, NL-1066 CX Amsterdam, Netherlands
[2] Univ Med Ctr, Dept Med Oncol, NL-3584 CG Utrecht, Netherlands
来源
BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON CANCER | 2008年 / 1786卷 / 01期
关键词
cyclin A; cyclin B1; Securin; Cdc20; Cdh1; pRb; Geminin; APC/C; Cyclosome; mitosis; cell cycle;
D O I
10.1016/j.bbcan.2008.05.002
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
For successful mitosis, Cyclin 131 and Securin must be degraded efficiently before anaphase. Destruction of these mitotic regulators by the 26S proteasome is the result of their poly-ubiquitination by a multi-subunit E3 ligase: the Anaphase-Promoting Complex or Cyclosome (APC/C). Clearly, the APC/C is not just important for mitosis. Destruction of APC/C substrates such as Cdc20, PIk1, Aurora A and Skp2 directs events in G1. Strikingly, the APC/C needs to stay active even in quiescent cells to keep them out of the cell cycle and forms an intriguing link with pRb. An inactive APC/C stabilizes Geminin, Cyclin A and Cyclin B1, thereby securing completion of DNA synthesis and progression through G2-phase. In prometaphase the APC/C becomes active again, but is controlled by the spindle assembly checkpoint. Here we discuss how the APC/C is either held in check or released. We argue that shedding more light on the APC/C is also important to understand cancer and could help the design of treatment. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:49 / 59
页数:11
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