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Activation of Cdh1‐dependent APC is required for G 1 cell cycle arrest and DNA damage‐induced G 2 checkpoint in vertebrate cells
Author(s) -
Sudo Tamotsu,
Ota Yosuke,
Kotani Shuji,
Nakao Mitsuyoshi,
Takami Yasunari,
Takeda Shunichi,
Saya Hideyuki
Publication year - 2001
Publication title -
the embo journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.484
H-Index - 392
eISSN - 1460-2075
pISSN - 0261-4189
DOI - 10.1093/emboj/20.22.6499
Subject(s) - biology , cdc20 , microbiology and biotechnology , g2 m dna damage checkpoint , cell cycle checkpoint , mitosis , cdh1 , anaphase promoting complex , dna damage , cyclin b , cell cycle , anaphase , cyclin , genetics , dna , cell , cadherin
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 . Further more, 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.