Quantitative proteomic analysis of purified yeast kinetochores identifies a PP1 regulatory subunit

被引:84
作者
Akiyoshi, Bungo [1 ,2 ]
Nelson, Christian R. [1 ]
Ranish, Jeffrey A. [3 ]
Biggins, Sue [1 ]
机构
[1] Fred Hutchinson Canc Res Ctr, Div Basic Sci, Seattle, WA 98109 USA
[2] Univ Washington, Mol & Cellular Biol Program, Seattle, WA 98195 USA
[3] Inst Syst Biol, Seattle, WA 98103 USA
关键词
Kinetochore; Ipl1/Aurora B protein kinase; PP1/Glc7 protein phosphatase I; Fin1; 14-3-3; SILAC quantitative mass spectrometry; TYPE-1 PROTEIN PHOSPHATASE; BUDDING YEAST; SACCHAROMYCES-CEREVISIAE; SPINDLE CHECKPOINT; CELL-CYCLE; KINASE; COMPLEX; PHOSPHORYLATION; FIN1; ARCHITECTURE;
D O I
10.1101/gad.1865909
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The kinetochore is a macromolecular complex that controls chromosome segregation and cell cycle progression. When sister kinetochores make bioriented attachments to microtubules from opposite poles, the spindle checkpoint is silenced. Biorientation and the spindle checkpoint are regulated by a balance between the Ipl1/Aurora B protein kinase and the opposing activity of protein phosphatase I (PP1). However, little is known about the regulation of PP1 localization and activity at the kinetochore. Here, we developed a method to purify centromere-bound kinetochores and used quantitative proteomics to identify the Fin1 protein as a PP1 regulatory subunit. The Fin1/PP1 complex is regulated by phosphorylation and 14-3-3 protein binding. When Fin1 is mislocalized, bipolar spindles fail to assemble but the spindle checkpoint is inappropriately silenced due to PP1 activity. These data suggest that Fin1 is a PP1 regulatory subunit whose spatial and temporal activity must be precisely controlled to ensure genomic stability.
引用
收藏
页码:2887 / 2899
页数:13
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