4.8 Article

Division of Labor between PCNA Loaders in DNA Replication and Sister Chromatid Cohesion Establishment

Journal

MOLECULAR CELL
Volume 78, Issue 4, Pages 725-+

Publisher

CELL PRESS
DOI: 10.1016/j.molcel.2020.03.017

Keywords

-

Funding

  1. European Research Council (ERC) [670412]
  2. Francis Crick Institute
  3. Cancer Research UK [FC001198]
  4. UK Medical Research Council [FC001198]
  5. Wellcome Trust [FC001198]

Ask authors/readers for more resources

Concomitant with DNA replication, the chromosomal cohesin complex establishes cohesion between newly replicated sister chromatids. Several replication-fork-associated cohesion establishment factors,'' including the multifunctional Ctf18-RFC complex, aid this process in as yet unknown ways. Here, we show that Ctf18-RFC's role in sister chromatid cohesion correlates with PCNA loading but is separable from its role in the replication checkpoint. Ctf18-RFC loads PCNA with a slight preference for the leading strand, which is dispensable for DNA replication. Conversely, the canonical Rfc1-RFC complex preferentially loads PCNA onto the lagging strand, which is crucial for DNA replication but dispensable for sister chromatid cohesion. The downstream effector of Ctf18-RFC is cohesin acetylation, which we place toward a late step during replication maturation. Our results suggest that Ctf18-RFC enriches and balances PCNA levels at the replication fork, beyond the needs of DNA replication, to promote establishment of sister chromatid cohesion and possibly other post-replicative processes.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available