共 50 条
Clb2 and the APC/CCdh1 regulate Swe1 stability
被引:0
|作者:
Simpson-Lavy, Kobi J.
[1
]
Brandeis, Michael
[1
]
机构:
[1] Hebrew Univ Jerusalem, Dept Genet, Alexander Silberman Inst Life Sci, IL-91904 Jerusalem, Israel
来源:
关键词:
S;
cervisiae;
Swe;
1;
Clb;
2;
Hsl;
Cdc5;
ANAPHASE-PROMOTING COMPLEX;
CDK-DEPENDENT PHOSPHORYLATION;
SACCHAROMYCES-CEREVISIAE;
BUDDING YEAST;
TYROSINE PHOSPHORYLATION;
MORPHOGENESIS CHECKPOINT;
DNA-REPLICATION;
PROTEIN-KINASE;
CYCLIN CLB2;
S-PHASE;
D O I:
10.4161/cc.9.115.12457
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
Swe1/Wee1 regulates mitotic entry by inhibiting Clb2-Cdk1 and its accumulation is involved in stress induced G(2) arrest. The APC/C-Cdh1 substrates Cdc5, Clb2 and Hsl1 regulate Swe1 degradation. We observed that clb2 Delta cdh1 Delta double mutant S. cerevisiae does not express any detectable levels of Swe1, presumably due to its constitutive degradation. This effect of Cdh1 inactivation is due to stabilization of Cdc5 and Hsl1, as expression of the non-degradable Cdc5(T29A) in clb2 Delta cells prevented Swe1 accumulation. Strikingly, expression of non-degradable Hsl1(mdb/mkb) prevented Swe1 accumulation even in wild type Clb2 cells. Interestingly Swe1 accumulation could be reconstituted in all these mutants by eliciting a replication fork stress with hydroxyurea. Cells expressing the Clb2(ME) mutant, that cannot bind Swe1, behaved like clb2 Delta cells, and failed to accumulate Swe1 in the absence of Cdh1 or the presence of Cdc5(T29A). This suggests that for Swe1 to accumulate it must interact with Clb2. We further show that in the absence of Clb2, Hsl1 is no longer essential for Swe1 degradation. We hypothesize that Clb2-Cdk1 protects Swe1 from premature degradation until its Hsl1 mediated de-protection, which enables its Cdc5 mediated degradation. Swe1 levels are thus regulated by monitoring the levels of three major mitotic regulators.
引用
收藏
页码:3046 / 3053
页数:8
相关论文