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Establishment of sister chromatid cohesion at the S-cerevisiae replication fork
被引:234
作者:
Lengronne, Armelle
McIntyre, John
Katou, Yuki
Kanoh, Yutaka
Hopfner, Karl-Peter
Shirahige, Katsuhiko
Uhlmann, Frank
机构:
[1] Canc Res UK London Res Inst, Chromosome Segregat Lab, Lincolns Inn Fields Labs, London WC2A 3PX, England
[2] Tokyo Inst Technol, Div Gene Res, Ctr Biol Resources & Informat, Midori Ku, Yokohama, Kanagawa 2268501, Japan
[3] Univ Munich, Gene Ctr, D-81377 Munich, Germany
[4] Univ Munich, Dept Chem & Biochem, D-81377 Munich, Germany
[5] CNRS, Inst Genet Humaine, F-34396 Montpellier, France
关键词:
D O I:
10.1016/j.molcel.2006.08.018
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:
Two identical sister copies of eukaryotic chromosomes are synthesized during S phase. To facilitate their recognition as pairs for segregation in mitosis, sister chromatids are held together from their synthesis onward by the chromosomal cohesin complex. Replication fork progression is thought to be coupled to establishment of sister chromatid cohesion, facilitating identification of replication products, but evidence for this has remained circumstantial. Here we show that three proteins required for sister chromatid cohesion, Eco1, Ctf4, and Ctf18, are found at, and Ctf4 travels along chromosomes with, replication forks. The ring-shaped cohesin complex is loaded onto chromosomes before S phase in an ATP hydrolysis-dependent reaction. Cohesion establishment during DNA replication follows without further cohesin recruitment and without need for cohesin to reengage an ATP hydrolysis motif that is critical for its initial DNA binding. This provides evidence for cohesion establishment in the context of replication forks and imposes constraints on the mechanism involved.
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页码:787 / 799
页数:13
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