Evidence map›Paper›PMID 21408204›Full record

ArticlePLoS genetics2011

Diverse roles and interactions of the SWI/SNF chromatin remodeling complex revealed using global approaches.

Ghia M Euskirchen, Raymond K Auerbach, Eugene Davidov, Tara A Gianoulis, Guoneng Zhong, Joel Rozowsky, Nitin Bhardwaj, Mark B Gerstein, Michael Snyder

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 150 papers.

0numbers the graph read from it
0cells of the map it votes in
150citing papers in PubMed
9.3field-weighted citation impact, top 1% 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

150 citing papers in PubMed, 219 citations in OpenAlex.

  1. Review
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  10. Identification and Development of BRD9 Chemical Probes.Pharmaceuticals (Basel, Switzerland) · 2024
    Review
  11. Article
  12. Review
  13. BCL11A Expression in Non-Small Cell Lung Cancers.International journal of molecular sciences · 2023
    Article
  14. Advances in the role of SWI/SNF complexes in tumours.Journal of cellular and molecular medicine · 2023
    Review
  15. Loss of the E3 ubiquitin ligases UBR-5 or HECD-1 restoresProceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. Article

90 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

9 authors at 4 institutions in 1 country.

Ghia M EuskirchenDepartment of Genetics, Stanford University School of Medicine, California, United States of America.
Raymond K Auerbach
Eugene Davidov
Tara A Gianoulis
Guoneng Zhong
Joel Rozowsky
Nitin Bhardwaj
Mark B Gerstein
Michael Snyder
Yale University · USStanford University · USHarvard University · USPerkinElmer (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A systems understanding of nuclear organization and events is critical for determining how cells divide, differentiate, and respond to stimuli and for identifying the causes of diseases. Chromatin remodeling complexes such as SWI/SNF have been implicated in a wide variety of cellular processes including gene expression, nuclear organization, centromere function, and chromosomal stability, and mutations in SWI/SNF components have been linked to several types of cancer. To better understand the biological processes in which chromatin remodeling proteins participate, we globally mapped binding regions for several components of the SWI/SNF complex throughout the human genome using ChIP-Seq. SWI/SNF components were found to lie near regulatory elements integral to transcription (e.g. 5' ends, RNA Polymerases II and III, and enhancers) as well as regions critical for chromosome organization (e.g. CTCF, lamins, and DNA replication origins). Interestingly we also find that certain configurations of SWI/SNF subunits are associated with transcripts that have higher levels of expression, whereas other configurations of SWI/SNF factors are associated with transcripts that have lower levels of expression. To further elucidate the association of SWI/SNF subunits with each other as well as with other nuclear proteins, we also analyzed SWI/SNF immunoprecipitated complexes by mass spectrometry. Individual SWI/SNF factors are associated with their own family members, as well as with cellular constituents such as nuclear matrix proteins, key transcription factors, and centromere components, implying a ubiquitous role in gene regulation and nuclear function. We find an overrepresentation of both SWI/SNF-associated regions and proteins in cell cycle and chromosome organization. Taken together the results from our ChIP and immunoprecipitation experiments suggest that SWI/SNF facilitates gene regulation and genome function more broadly and through a greater diversity of interactions than previously appreciated.

Indexed as

ChromatinChromosomal Proteins, Non-HistoneTranscription FactorsCell CycleChromatin Assembly and DisassemblyChromatin ImmunoprecipitationHeLa CellsHigh-Throughput Nucleotide SequencingHumansNuclear ProteinsProtein BindingSequence Analysis, DNAChromatinChromosomal Proteins, Non-HistoneNuclear ProteinsSWI-SNF-B chromatin-remodeling complexTranscription Factors

Identifiers

PMID21408204
PMCPMC3048368
OpenAlexW2069237225

What OpenQuestion holds

Textmetadata
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.