Evidence map›Paper›PMID 25173104›Full record

ArticleNature genetics2014

The Scc2-Scc4 complex acts in sister chromatid cohesion and transcriptional regulation by maintaining nucleosome-free regions.

Lidia Lopez-Serra, Gavin Kelly, Harshil Patel, Aengus Stewart, Frank Uhlmann

Open access · greenAbstract read
In one paragraph

Article in Nature genetics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 85 papers.

0numbers the graph read from it
0cells of the map it votes in
85citing papers in PubMed
7.1field-weighted citation impact, top 2% 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

85 citing papers in PubMed, 129 citations in OpenAlex.

  1. Trial
  2. Article
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  5. Article
  6. Aberrant cohesin function inbioRxiv : the preprint server for biology · 2025
    Article
  7. Article
  8. Review
  9. Review
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  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
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  18. Review
  19. SMC complexes: Lifting the lid on loop extrusion.Current opinion in cell biology · 2022
    Review
  20. Review

25 more citing papers are in PubMed but not listed here.

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

5 authors at 1 institution in 1 country.

Lidia Lopez-SerraChromosome Segregation Laboratory, Cancer Research UK London Research Institute, London, UK.
Gavin KellyBioinformatics and Biostatistics Service, Cancer Research UK London Research Institute, London, UK.
Harshil PatelBioinformatics and Biostatistics Service, Cancer Research UK London Research Institute, London, UK.
Aengus StewartBioinformatics and Biostatistics Service, Cancer Research UK London Research Institute, London, UK.
Frank UhlmannChromosome Segregation Laboratory, Cancer Research UK London Research Institute, London, UK.
Cancer Research UK · GB

Funding

Cancer Research UK 15671Cancer Research UK A3592European Research Council 249777
6 · The paper itself

Abstract

The cohesin complex is at the heart of many chromosomal activities, including sister chromatid cohesion and transcriptional regulation. Cohesin loading onto chromosomes depends on the Scc2-Scc4 cohesin loader complex, but the chromatin features that form cohesin loading sites remain poorly understood. Here we show that the RSC chromatin remodeling complex recruits budding yeast Scc2-Scc4 to broad nucleosome-free regions, which the cohesin loader helps to maintain. Consequently, inactivation of either the cohesin loader or the RSC complex has similar effects on nucleosome positioning, gene expression and sister chromatid cohesion. These results show an intimate link between local chromatin structure and higher-order chromosome architecture. Our findings pertain to the similarities between two severe human disorders, Cornelia de Lange syndrome, which is caused by alterations in the human cohesin loader, and Coffin-Siris syndrome, which results from alterations in human RSC complex components. Both syndromes can arise from gene misregulation due to related changes in the nucleosome landscape.

Indexed as

Gene Expression Regulation, FungalAbnormalities, MultipleBinding SitesChromatidsChromatinChromosomal Proteins, Non-HistoneChromosomes, FungalDe Lange SyndromeFaceGene Expression ProfilingHand Deformities, CongenitalHumansIntellectual DisabilityMicrognathismNeckNucleosomesChromatinChromosomal Proteins, Non-HistoneNucleosomesSaccharomyces cerevisiae ProteinsSCC2 protein, S cerevisiaeSCC4 protein, S cerevisiae

Identifiers

PMID25173104
PMCPMC4177232
OpenAlexW1996413778

What OpenQuestion holds

Textmetadata
LicenceTDM
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.