Sister chromatid separation and chromosome re-duplication are regulated by different mechanisms in response to spindle damage

被引:167
作者
Alexandru, G [1 ]
Zachariae, W [1 ]
Schleiffer, A [1 ]
Nasmyth, K [1 ]
机构
[1] Res Inst Mol Pathol, A-1030 Vienna, Austria
关键词
Bub2; cell cycle arrest; Mad2; spindle checkpoint;
D O I
10.1093/emboj/18.10.2707
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
In yeast, anaphase entry depends on Pds1 proteolysis, while chromosome re-duplication in the subsequent S-phase involves degradation of mitotic cyclins such as Clb2, Sequential proteolysis of Pds1 and mitotic cyclins is mediated by the anaphase-promoting complex (APC), Lagging chromosomes or spindle damage are detected by surveillance mechanisms (checkpoints) which block anaphase onset, cytokinesis and DNA re-replication. Until now, the MAD and BUB genes implicated in this regulation were thought to function in a single pathway that blocks APC activity. We show that spindle damage blocks sister chromatid separation solely by inhibiting APC(Cdc20)-dependent Pds1 proteolysis and that this process requires Mad2. Blocking APC(Cdh1)-mediated Clb2 proteolysis and chromosome re-duplication does not require Mad2 but a different protein, Bub2, Our data imply that Mad1, Mad2, Mad3 and Bub1 regulate ApC(Cdc20), whereas Bub2 regulates ApC(Cdh1).
引用
收藏
页码:2707 / 2721
页数:15
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