Requirement of Skp1-Bub1 interaction for kinetochore- mediated activation of the spindle checkpoint

被引:40
作者
Kitagawa, K
Abdulle, R
Bansal, PK
Cagney, G
Fields, S
Hieter, P
机构
[1] St Jude Childrens Res Hosp, Dept Mol Pharmacol, Memphis, TN 38105 USA
[2] Univ Washington, Dept Genome Sci & Med, Seattle, WA 98195 USA
[3] Univ Washington, Howard Hughes Med Inst, Seattle, WA 98195 USA
[4] Univ British Columbia, UBC Biotechnol Lab, Dept Med Genet, Vancouver, BC V5Z 4H4, Canada
[5] Univ British Columbia, Ctr Mol Med & Therapeut, Vancouver, BC V5Z 4H4, Canada
关键词
D O I
10.1016/S1097-2765(03)00145-X
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
The spindle checkpoint transiently prevents cell cycle progression of cells that have incurred errors or failed to complete steps during mitosis, including those involving kinetochore function. The molecular nature of the primary signal transmitted from defective kinetochores and how it is detected by the spindle checkpoint are unknown. We report biochemical evidence that Bub1, a component of the spindle checkpoint, associates with centromere (CEN) DNA via Skp1, a core kinetochore component in budding yeast. The Skp1's interaction with Bub1 is required for the mitotic delay induced by kinetochore tension defects, but not for the arrest induced by spindle depolymerization, kinetochore assembly defects, or Mps1 overexpression. We propose that the Skp1-Bub1 interaction Is important for transmitting a signal to the spindle checkpoint pathway when insufficient tension is present at kinetochores.
引用
收藏
页码:1201 / 1213
页数:13
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