Evidence map›Paper›PMID 17502338›Full record

ArticleJournal of leukocyte biology2007

Modulation of NFAT-dependent gene expression by the RhoA signaling pathway in T cells.

Whitney S Helms, Jerry L Jeffrey, Derek A Holmes, Michael B Townsend, Neil A Clipstone, Lishan Su

Abstract read
In one paragraph

Article in Journal of leukocyte biology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
0.3field-weighted citation impact, top 41% 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

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 24 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Review
  8. Article
  9. Function and regulation of microRNA-31 in development and disease.Molecular reproduction and development · 2016
    Review
  10. Review
  11. Review
  12. Review
  13. GnRH regulation of Jun and Atf3 requires calcium, calcineurin, and NFAT.Molecular endocrinology (Baltimore, Md.) · 2012
    Article
  14. Review
  15. Review
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

6 authors at 2 institutions in 1 country.

Whitney S HelmsDepartment of Microbiology and Immunology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599-7295, USA.
Jerry L Jeffrey
Derek A Holmes
Michael B Townsend
Neil A Clipstone
Lishan Su
University of North Carolina at Chapel Hill · USUNC Lineberger Comprehensive Cancer Center

Funding

BASIC IMMUNE MECHANISMST32AI007273 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI TISCH, ROLAND M · 1985 to 2020
$5.6M
RHOA EFFECTOR IN HIV-1 REPLICATION AND PATHOGENESISR01AI048407 · NIAID · UNIVERSITY OF NORTH CAROLINA CHAPEL HILL · PI SU, LISHAN · 2000 to 2004
$1.6M
Treg in HIV-1 Replication and PathogenesisR01AI077454 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI SU, LISHAN · 2008 to 2011
$1.5M
Genetic Analy. of Chemokine Receptors in T Cell Develop.R21AI053804 · NIAID · UNIVERSITY OF NORTH CAROLINA CHAPEL HILL · PI SU, LISHAN · 2002 to 2003
$361k
NIAID NIH HHS 5T32AI07273NIAID NIH HHS AI04840704NIAID NIH HHS AI5380402NIAID NIH HHS R01 AI048407NIAID NIH HHS R01 AI077454NIAID NIH HHS T32 AI007273
6 · The paper itself

Abstract

We have reported previously that p115Rho guanine nucleotide exchange factor, its upstream activator Galpha13, and its effector RhoA are able to inhibit HIV-1 replication. Here, we show that RhoA is able to inhibit HIV-1 gene expression through the NFAT-binding site in the HIV long-terminal repeat. Constitutively active NFAT counteracts the inhibitory activity of RhoA, and inhibition of NFAT activation also inhibits HIV-1 gene expression. We have shown further that RhoA inhibits NFAT-dependent transcription and IL-2 production in human T cells. RhoA does not inhibit nuclear localization of NFAT but rather, inhibits its transcriptional activity. In addition, RhoA decreases the level of acetylated histone H3, but not NFAT occupancy, at the IL-2 promoter. These data suggest that activation of RhoA can modulate IL-2 gene expression by inhibiting the transcriptional activity of NFAT and chromatin structure at the IL-2 promoter during T cell activation.

Indexed as

Gene Expression RegulationSignal TransductionGenes, ReporterHIV Long Terminal RepeatHumansJurkat CellsLuciferasesNFATC Transcription FactorsRetroviridaerhoA GTP-Binding ProteinT-LymphocytesTransduction, GeneticLuciferasesNFATC Transcription FactorsrhoA GTP-Binding Protein

Identifiers

PMID17502338
PMCPMC4418492
OpenAlexW2058315397

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.