Activation of Cdh1-dependent APC is required for G1 cell cycle arrest and DNA damage-induced G2 checkpoint in vertebrate cells

被引:128
作者
Sudo, T
Ota, Y
Kotani, S
Nakao, M
Takami, Y
Takeda, S
Saya, H
机构
[1] Kumamoto Univ, Sch Med, Dept Tumor Genet & Biol, Kumamoto 8600811, Japan
[2] RIKEN, Genome Sci Ctr, Bioinformat Grp, Tsurumi Ku, Yokohama, Kanagawa 2300045, Japan
[3] Miyazaki Med Coll, Dept Biochem, Miyazaki 8891692, Japan
[4] Kyoto Univ, Fac Med, Dept Radiat Genet, Sakyo Ku, Kyoto 6068501, Japan
关键词
Cdc27; DT40; mitotic cyclin; p27; rapamycin;
D O I
10.1093/emboj/20.22.6499
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
Anaphase-promoting complex (APC) is activated by two regulatory proteins, Cdc20 and Cdh1. In yeast and Drosophila, Cdh1-dependent APC (Cdh1-APC) activity targets mitotic cyclins from the end of mitosis to the G(1) phase. To investigate the function of Cdh1 in vertebrate cells, we generated clones of chicken DT40 cells disrupted in their Cdh1 loci. Cdh1 was dispensable for viability and cell cycle progression. However, similarly to yeast and Drosophila, loss of Cdh1 induced unscheduled accumulation of mitotic cyclins in G(1), resulting in abrogation of G(1) arrest caused by treatment with rapamycin, an inducer of p27(Kip1). Furthermore, we found that Cdh1(-/-) cells fail to maintain DNA damage-induced G(2) arrest and that Cdh1-APC is activated by X-irradiation-induced DNA damage. Thus, activation of Cdh1-APC plays a crucial role in both cdk inhibitor-dependent G(1) arrest and DNA damage-induced G(2) arrest.
引用
收藏
页码:6499 / 6508
页数:10
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