Identification of RFC(Ctf18p, Ctf8p, Dcc1p):: An alternative RFC complex required for sister chromatid cohesion in S-cerevisiae

被引:281
作者
Mayer, ML
Gygi, SP
Aebersold, R
Hieter, P [1 ]
机构
[1] Johns Hopkins Univ, Sch Med, Grad Program Biochem Cellular & Mol Biol, Baltimore, MD 21205 USA
[2] Harvard Univ, Sch Med, Dept Cell Biol, Boston, MA 02115 USA
[3] Inst Syst Biol Seattle, Seattle, WA 98105 USA
[4] Univ British Columbia, Biotechnol Lab, Vancouver, BC V6T 1Z3, Canada
[5] Ctr Mol Med & Therapeut, Vancouver, BC V5Z 4H4, Canada
关键词
D O I
10.1016/S1097-2765(01)00254-4
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
We have identified and characterized an alternative RFC complex RFC(Ctf18p, Ctf8p, Dcc1p) that is required for sister chromatid cohesion and faithful chromosome transmission. Ctf18p, Ctf8p, and Dcc1p interact physically in a complex with Rfc2p, Rfc3p, Rfc4p, and Rfc5p but not with Rfc1p or Rad24p. Deletion of CTF18, CTF8, or DCC1 singly or in combination (ctf18 Delta ctf8 Delta dcc1 Delta) leads to sensitivity to microtubule depolymerizing drugs and a severe sister chromatid cohesion defect. Furthermore, temperature-sensitive mutations in RFC4 result in precocious sister chromatid separation. Our results highlight a novel function of the RFC proteins and support a model in which sister chromatid cohesion is established at the replication fork via a polymerase switching mechanism and a replication-coupled remodeling of chromatin.
引用
收藏
页码:959 / 970
页数:12
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