Evidence map›Paper›PMID 22495890›Full record

ArticleBiology of reproduction2012

Essential roles of the chromatin remodeling factor BRG1 in spermatogenesis in mice.

Jianguan Wang, Honggang Gu, Haifan Lin, Tian Chi

Open access · bronzeAbstract read
In one paragraph

Article in Biology of reproduction, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

30 citing papers in PubMed, 51 citations in OpenAlex.

  1. Characterization ofBiomolecules · 2026
    Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Exploring the potential ofCurrent research in toxicology · 2025
    Article
  7. Article
  8. Article
  9. Article
  10. Envisioning a role for nuclear actin in prophase I spermatocytes.Frontiers in cell and developmental biology · 2023
    Review
  11. Article
  12. Article
  13. Review
  14. Article
  15. Review
  16. Article
  17. BRG1 Is Dispensable for Sertoli Cell Development and Functions in Mice.International journal of molecular sciences · 2020
    Article
  18. CDK2 regulates the NRF1/The Journal of cell biology · 2019
    Article
  19. Article
  20. Article
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

4 authors at 2 institutions in 2 countries.

Jianguan WangDepartment of Cell Biology, Yale University, New Haven, Connecticut, USA.
Honggang Gu
Haifan Lin
Tian Chi
Yale University · USLonghua Hospital Shanghai University of Traditional Chinese Medicine · CN

Funding

Stem Cell Mechanism in the Murine GermlineR01HD042012 · NICHD · YALE UNIVERSITY · PI QI, HONGYING · 2002 to 2022
$4.2M
Epimutation at the CD4 locus: induction, propagation and repairR21AI094000 · NIAID · YALE UNIVERSITY · PI CHI, TIAN H · 2011 to 2012
$455k
NIAID NIH HHS 5R21AI094000-02NIAID NIH HHS R21 AI094000NICHD NIH HHS R01 HD042012NICHD NIH HHS R01HD42012
6 · The paper itself

Abstract

Mammalian spermatogenesis is a complex process that involves spatiotemporal regulation of gene expression and meiotic recombination, both of which require the modulation of chromatin structure. Proteins important for chromatin regulation during spermatogenesis remain poorly understood. Here we addressed the role of BRG1, the catalytic subunit of the mammalian Swi/Snf-like BAF chromatin-remodeling complex, during spermatogenesis in mice. BRG1 expression is dynamically regulated in the male germline, being weakly detectable in spermatogonia, highly expressed in pachytene spermatocytes, and turned off in maturing round spermatids. This expression pattern overlaps that of Brm, the Brg1 homolog. While Brm knockout males are known to be fertile, germline-specific Brg1 deletion completely arrests spermatogenesis at the midpachytene stage, which is associated with spermatocyte apoptosis and apparently also with impaired homologous recombination and meiotic sex chromosome inactivation. However, Brg1 is dispensable for gammaH2AX formation during meiotic recombination, contrary to its reported role in DNA repair in somatic cells. Our study reveals the essential role of Brg1 in meiosis and underscores the differences in the mechanisms of DNA repair between germ cells and somatic cells.

Indexed as

SpermatogenesisAnimalsApoptosisChromatin Assembly and DisassemblyDNA HelicasesGene DeletionGene Knockout TechniquesHistonesMaleMiceNuclear ProteinsPachytene StageRecombination, GeneticSpermatocytesTestisTranscription FactorsDNA Helicasesgamma-H2AX protein, mouseHistonesNuclear ProteinsSmarca2 protein, mouseSmarca4 protein, mouseTranscription Factors

Identifiers

PMID22495890
PMCPMC3386149
OpenAlexW2145375982

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.