Rca1 inhibits APC-Cdh1Fzr and is required to prevent cyclin degradation in G2

被引：94

作者：

Grosskortenhaus, R ^{[1
]}

Sprenger, F ^{[1
]}

机构：

[1] Univ Cologne, Dept Genet, D-50931 Cologne, Germany

来源：

DEVELOPMENTAL CELL | 2002年 / 2卷 / 01期

关键词：

D O I：

10.1016/S1534-5807(01)00104-6

中图分类号：

Q2 [细胞生物学];

学科分类号：

071009 ; 090102 ;

摘要：

We demonstrate that Rca1 is an essential inhibitor of the anaphase-promoting complex/cyclosome (APC) in Drosophila. APC activity is restricted to mitotic stages and G1 by its activators Cdc20-Fizzy (Cdc20(Fzy)) and Cdh1-Fizzy-related (Cdh1(Fzr)), respectively. In rca1 mutants, cyclins are degraded prematurely in G2 by APC-Cdh1(Fzr)-dependent proteolysis, and cells fail to execute mitosis. Overexpression of Cdh1(Fzr) mimics the rca1 phenotype, and coexpression of Rca1 blocks this Cdh1(Fzr) function. We show that Rca1 and Cdh1(Fzr) are in a complex that also includes the APC component Cdc27. Previous studies have shown that phosphorylation of Cdh1 prevents its interaction with the APC. Our data reveal a different mode of APC regulation by Rca1 at the G2 stage, when low Cdk activity is unable to inhibit Cdh1(Fzr) interaction.

引用

页码：29 / 40

页数：12

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