Emi1 is a mitotic regulator that interacts with Cdc20 and inhibits the anaphase promoting complex

被引:317
作者
Reimann, JDR
Freed, E
Hsu, JY
Kramer, ER
Peters, JM
Jackson, PK
机构
[1] Stanford Univ, Sch Med, Dept Pathol, Stanford, CA 94305 USA
[2] Stanford Univ, Sch Med, Dept Microbiol & Immunol, Stanford, CA 94305 USA
[3] Stanford Univ, Sch Med, Dept Canc Biol, Stanford, CA 94305 USA
[4] Stanford Univ, Sch Med, Dept Biophys, Stanford, CA 94305 USA
[5] Res Inst Mol Pathol, A-1030 Vienna, Austria
关键词
D O I
10.1016/S0092-8674(01)00361-0
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
We have discovered an early mitotic inhibitor, Emi1, which regulates mitosis by inhibiting the anaphase promoting complex/cyclosome (APC). Emi1 is a conserved F box protein containing a zinc binding region essential for APC inhibition. Emi1 accumulates before mitosis and is ubiquitylated and destroyed in mitosis, independent of the APC. Emi1 immunodepletion from cycling Xenopus extracts strongly delays cyclin B accumulation and mitotic entry, whereas nondestructible Emi1 stabilizes APC substrates and causes a mitotic block. Emi1 binds the APC activator Cdc20, and Cdc20 can rescue an Emi1-induced block to cyclin B destruction. Our results suggest that Emi1 regulates progression through early mitosis by preventing premature APC activation, and may help explain the well-known delay between cyclin B/Cdc2 activation and cyclin B destruction.
引用
收藏
页码:645 / 655
页数:11
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