Evidence map›Paper›PMID 35654035›Full record

ArticleCurrent biology : CB2022

Mediator recruits the cohesin loader Scc2 to RNA Pol II-transcribed genes and promotes sister chromatid cohesion.

Mark Mattingly, Chris Seidel, Sofía Muñoz, Yan Hao, Ying Zhang, Zhihui Wen, Laurence Florens, Frank Uhlmann, Jennifer L Gerton

Open access · bronzeAbstract read
In one paragraph

Article in Current biology : CB, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

19 citing papers in PubMed, 29 citations in OpenAlex.

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  9. Liquid condensates: a new barrier to loop extrusion?Cellular and molecular life sciences : CMLS · 2025
    Review
  10. Article
  11. Article
  12. Cohesin organizes 3D DNA contacts surrounding active enhancers inbioRxiv : the preprint server for biology · 2024
    Article
  13. The Wild West of spike-in normalization.Nature biotechnology · 2024
    Article
  14. 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

9 authors at 2 institutions in 2 countries.

Mark MattinglyStowers Institute for Medical Research, Kansas City, MO 64110, USA.
Chris SeidelStowers Institute for Medical Research, Kansas City, MO 64110, USA.
Sofía MuñozChromosome Segregation Laboratory, The Francis Crick Institute, London NW1 1AT, UK.
Yan HaoStowers Institute for Medical Research, Kansas City, MO 64110, USA.
Ying ZhangStowers Institute for Medical Research, Kansas City, MO 64110, USA.
Zhihui WenStowers Institute for Medical Research, Kansas City, MO 64110, USA.
Laurence FlorensStowers Institute for Medical Research, Kansas City, MO 64110, USA.
Frank UhlmannChromosome Segregation Laboratory, The Francis Crick Institute, London NW1 1AT, UK.
Jennifer L GertonStowers Institute for Medical Research, Kansas City, MO 64110, USA; Department of Biochemistry and Molecular Biology, University of Kansas Medical Center, Kansas City, KS 66160, USA. Electronic address: jeg@stowers.org.
Stowers Institute for Medical Research · USThe Francis Crick Institute · GB

Funding

Cancer Research UK 15671Medical Research CouncilWellcome Trust FC001198
6 · The paper itself

Abstract

The ring-like cohesin complex plays an essential role in chromosome segregation, organization, and double-strand break repair through its ability to bring two DNA double helices together. Scc2 (NIPBL in humans) together with Scc4 functions as the loader of cohesin onto chromosomes. Chromatin adapters such as the RSC complex facilitate the localization of the Scc2-Scc4 cohesin loader. Here, we identify a broad range of Scc2-chromatin protein interactions that are evolutionarily conserved and reveal a role for one complex, Mediator, in the recruitment of the cohesin loader. We identified budding yeast Med14, a subunit of the Mediator complex, as a high copy suppressor of poor growth in Scc2 mutant strains. Physical and genetic interactions between Scc2 and Mediator are functionally substantiated in direct recruitment and cohesion assays. Depletion of Med14 results in defective sister chromatid cohesion and the decreased binding of Scc2 at RNA Pol II-transcribed genes. Previous work has suggested that Mediator, Nipbl, and cohesin connect enhancers and promoters of active mammalian genes. Our studies suggest an evolutionarily conserved fundamental role for Mediator in the direct recruitment of Scc2 to RNA Pol II-transcribed genes.

Indexed as

Chromosome SegregationSaccharomyces cerevisiae ProteinsAnimalsCell Cycle ProteinsChromatidsChromatinChromosomal Proteins, Non-HistoneCohesinsHumansMammalsRNA Polymerase IISaccharomyces cerevisiaeCell Cycle ProteinsChromatinChromosomal Proteins, Non-HistoneCohesinsNIPBL protein, humanRNA Polymerase IISaccharomyces cerevisiae ProteinsSCC2 protein, S cerevisiaeSCC4 protein, S cerevisiaechromatin adapterscohesincohesin loaderMed14MediatorSaccharomyces cerevisiaeScc2-Scc4sister chromatid cohesion

Identifiers

PMID35654035
PMCPMC9286023
OpenAlexW4281862425

What Socratic holds

Textmetadata
LicenceCC BY-NC
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 Socratic graph.