Evidence map›Paper›PMID 18955569›Full record

ArticleThe Journal of experimental medicine2008

A novel genetic strategy reveals unexpected roles of the Swi-Snf-like chromatin-remodeling BAF complex in thymocyte development.

Anant Jani, Mimi Wan, Jianmin Zhang, Kairong Cui, Jie Wu, Paula Preston-Hurlburt, Rohini Khatri, Keji Zhao, Tian Chi

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

21 citing papers in PubMed, 33 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. The Loss of TET2 Promotes CD8Journal of immunology (Baltimore, Md. : 1950) · 2018
    Article
  8. BPTF Is Essential for T Cell Homeostasis and Function.Journal of immunology (Baltimore, Md. : 1950) · 2016
    Article
  9. Review
  10. Article
  11. Combined gene dosage requirement for SWI/SNF catalytic subunits during early mammalian development.Mammalian genome : official journal of the International Mammalian Genome Society · 2013
    Article
  12. Article
  13. Article
  14. Article
  15. ATP-dependent chromatin remodeling in T cells.Biochemistry and cell biology = Biochimie et biologie cellulaire · 2012
    Review
  16. Review
  17. Article
  18. 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

9 authors at 3 institutions in 1 country.

Anant JaniDepartment of Immunobiology, Yale University Medical School, New Haven, CT 06520, USA.
Mimi Wan
Jianmin Zhang
Kairong Cui
Jie Wu
Paula Preston-Hurlburt
Rohini Khatri
Keji Zhao
Tian Chi
Yale University · USNational Heart Lung and Blood Institute · USNational Institutes of Health · US

Funding

Genome-wide mapping of histone modificationsZIAHL005801 · NHLBI · NATIONAL HEART, LUNG, AND BLOOD INSTITUTE · PI ZHAO, KEJI · 2009 to 2025
$24.0M
BAF complexes in T cell developmentR01AI063554 · NIAID · YALE UNIVERSITY · PI CHI, TIAN H · 2005 to 2009
$1.9M
Intramural NIH HHSNIAID NIH HHS R01 AI063554NIAID NIH HHS R01AI063554-02
6 · The paper itself

Abstract

We have developed a general strategy for creating littermates bearing either a tissue-specific point mutation or deletion in any target gene, and used the method to dissect the roles of Brg, the ATPase subunit of the chromatin-remodeling Brg-associated factor (BAF) complex, in early thymocyte development. We found that a point mutation that inactivates the Brg ATPase recapitulates multiple defects previously described for Brg deletion (Chi, T.H., M. Wan, P.P. Lee, K. Akashi, D. Metzger, P. Chambon, C.B. Wilson, and G.R. Crabtree. 2003. Immunity. 19:169-182). However, the point mutant helps reveal unexpected roles of Brg in CD25 repression and CD4 activation. Surprisingly, CD4 activation occurs independently of the Brg ATPase and is perhaps mediated by physical interactions between Brg and the CD4 locus. Our study thus suggests that the BAF complex harbors novel activities that can be necessary and even sufficient for stimulating transcription from an endogenous chromatin template in the absence of Brg-dependent remodeling of that template. We conclude that conditional point mutants, rarely used in mammalian genetics, can help uncover important gene functions undetectable or overlooked in deletion mutants.

Indexed as

Chromosomal Proteins, Non-HistonePoint MutationThymus GlandTranscription FactorsAnimalsbcl-X ProteinCD4 AntigensChromatinDNA HelicasesGene DeletionGene Expression RegulationMiceMice, Inbred C57BLMice, TransgenicNuclear ProteinsPhenotypeBcl2l1 protein, mousebcl-X ProteinCD4 AntigensChromatinChromosomal Proteins, Non-HistoneDNA HelicasesNuclear ProteinsSmarca4 protein, mouseSWI-SNF-B chromatin-remodeling complexTranscription Factors

Identifiers

PMID18955569
PMCPMC2585832
OpenAlexW2137008073

What OpenQuestion holds

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LicenceCC BY-NC-SA
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.