Identification of protein complexes required for efficient sister chromatid cohesion

被引:201
作者
Mayer, ML
Pot, I
Chang, M
Xu, H
Aneliunas, V
Kwok, T
Newitt, R
Aebersold, R
Boone, C
Brown, GW
Hieter, P [1 ]
机构
[1] Univ British Columbia, Ctr Mol Med & Therapeut, Vancouver, BC V5Z 4H4, Canada
[2] Univ British Columbia, Biotechnol Lab, Vancouver, BC V6T 1Z3, Canada
[3] Univ British Columbia, Dept Biochem & Mol Biol, Vancouver, BC V6T 1Z3, Canada
[4] Univ Toronto, Dept Biochem, Toronto, ON M5S 1A8, Canada
[5] Univ Toronto, Dept Med Genet & Microbiol, Toronto, ON M5S 1A8, Canada
[6] Univ Toronto, Banting & Best Dept Med Res, Toronto, ON M5G 1L6, Canada
[7] Inst Syst Biol, Seattle, WA 98105 USA
关键词
D O I
10.1091/mbc.E03-08-0619
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Ctf8p is a component of Ctf18-RFC, an alternative replication factor C-like complex required for efficient sister chromatid cohesion in Saccharomyces cerevisiae. We performed synthetic genetic array (SGA) analysis with a ctf8 deletion strain as a primary screen to identify other nonessential genes required for efficient sister chromatid cohesion. We then assessed proficiency of cohesion at three chromosomal loci in strains containing deletions of the genes identified in the ctf8 SGA screen. Deletion of seven genes (CHL1, CSM3, BIM1, KAR3, TOF1, CTF4, and VIK1) resulted in defective sister chromatid cohesion. Mass spectrometric analysis of immunoprecipitated complexes identified a physical association between Kar3p and Vik1p and an interaction between Csm3p and Tof1p that we confirmed by coimmunoprecipitation from cell extracts. These data indicate that synthetic genetic array analysis coupled with specific secondary screens can effectively identify protein complexes functionally related to a reference gene. Furthermore, we find that genes involved in mitotic spindle integrity and positioning have a previously unrecognized role in sister chromatid cohesion.
引用
收藏
页码:1736 / 1745
页数:10
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