Evidence map›Paper›PMID 32277910›Full record

ArticleMolecular cell2020

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

Hon Wing Liu, Céline Bouchoux, Mélanie Panarotto, Yasutaka Kakui, Harshil Patel, Frank Uhlmann

Open access · hybridAbstract read
In one paragraph

Article in Molecular cell, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
3.6field-weighted citation impact, top 6% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

45 citing papers in PubMed, 66 citations in OpenAlex.

  1. Article
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  7. Biochemical Reconstitution of Replication-Coupled Cohesin Acetylation.Methods in molecular biology (Clifton, N.J.) · 2026
    Article
  8. Structure of the human CTF18-RFC clamp loader bound to PCNA.bioRxiv : the preprint server for biology · 2025
    Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Cryo-EM reveals a nearly complete PCNA loading process and unique features of the human alternative clamp loader CTF18-RFC.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  15. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 1 institution in 1 country.

Hon Wing LiuChromosome Segregation Laboratory, The Francis Crick Institute, 1 Midland Road, London NW1 1AT, UK.
Céline BouchouxChromosome Segregation Laboratory, The Francis Crick Institute, 1 Midland Road, London NW1 1AT, UK.
Mélanie PanarottoChromosome Segregation Laboratory, The Francis Crick Institute, 1 Midland Road, London NW1 1AT, UK.
Yasutaka KakuiChromosome Segregation Laboratory, The Francis Crick Institute, 1 Midland Road, London NW1 1AT, UK.
Harshil PatelBioinformatics and Biostatistics Science Technology Platform, The Francis Crick Institute, 1 Midland Road, London NW1 1AT, UK.
Frank UhlmannChromosome Segregation Laboratory, The Francis Crick Institute, 1 Midland Road, London NW1 1AT, UK. Electronic address: frank.uhlmann@crick.ac.uk.
The Francis Crick Institute · GB

Funding

Cancer Research UK FC001198Medical Research Council FC001198Wellcome TrustWellcome Trust FC001198
6 · The paper itself

Abstract

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.

Indexed as

DNA ReplicationAcetyltransferasesCell Cycle ProteinsChromatidsChromosomal Proteins, Non-HistoneChromosome SegregationChromosomes, FungalCohesinsNuclear ProteinsProliferating Cell Nuclear AntigenReplication Protein CSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsAcetyltransferasesCell Cycle ProteinsChromosomal Proteins, Non-HistoneCohesinsCTF18 protein, S cerevisiaeECO1 protein, S cerevisiaeNuclear ProteinsPOL30 protein, S cerevisiaeProliferating Cell Nuclear AntigenReplication Protein CRFC1 protein, S cerevisiaeSaccharomyces cerevisiae ProteinsChromosome SegregationCohesion EstablishmentCtf18DNA ReplicationEco1PCNAReplication Factor CRfc1S. cerevisiaeSister Chromatid Cohesion

Identifiers

PMID32277910
PMCPMC7242910
OpenAlexW3002073397

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.