Hos1 Deacetylates Smc3 to Close the Cohesin Acetylation Cycle

被引:89
作者
Borges, Vanessa [1 ]
Lehane, Chris [1 ]
Lopez-Serra, Lidia [1 ]
Flynn, Helen [2 ]
Skehel, Mark [2 ]
Ben-Shahar, Tom Rolef [1 ]
Uhlmann, Frank [1 ]
机构
[1] Canc Res UK London Res Inst, Chromosome Segregat Lab, Lincolns Inn Fields Labs, London WC2A 3PX, England
[2] Canc Res UK London Res Inst, Clare Hall Labs, S Mimms EN6 3LD, Herts, England
关键词
SISTER-CHROMATID COHESION; SACCHAROMYCES-CEREVISIAE; HISTONE DEACETYLASES; DNA-REPLICATION; S-PHASE; GENE ACTIVATION; YEAST; COMPLEX; ESTABLISHMENT; PROTEIN;
D O I
10.1016/j.molcel.2010.08.009
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
Cohesion between sister chromatids is mediated by the chromosomal cohesin complex. In budding yeast, cohesin is loaded onto chromosomes during the G1 phase of the cell cycle. During S phase, the replication fork-associated acetyltransferase Eco1 acetylates the cohesin subunit Smc3 to promote the establishment of sister chromatid cohesion. At the time of anaphase, Smc3 loses its acetylation again, but the Smc3 deacetylase and the possible importance of Smc3 deacetylation are unknown. Here, we show that the class I histone deacetylase family member Hos1 is responsible for Smc3 deacetylation. Cohesin is protected from deacetylation while bound to chromosomes but is deacetylated as soon as it dissociates from chromosomes at anaphase onset. Nonacetylated Smc3 is required as a substrate for cohesion establishment in the following cell cycle. Our results complete the description of an Smc3 acetylation cycle and provide unexpected insight into the importance of de novo Smc3 acetylation for cohesion establishment.
引用
收藏
页码:677 / 688
页数:12
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