Evidence map›Paper›PMID 19196836›Full record

ArticleMolecular endocrinology (Baltimore, Md.)2009

Negative regulation of TSHalpha target gene by thyroid hormone involves histone acetylation and corepressor complex dissociation.

Dongqing Wang, Xianmin Xia, Ying Liu, Alexis Oetting, Robert L Walker, Yuelin Zhu, Paul Meltzer, Philip A Cole, Yun-Bo Shi, Paul M Yen

Open access · bronzeAbstract read
In one paragraph

Article in Molecular endocrinology (Baltimore, Md.), 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

17 citing papers in PubMed, 42 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Recent advances in central congenital hypothyroidism.The Journal of endocrinology · 2015
    Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Cardiac myosin heavy chain gene regulation by thyroid hormone involves altered histone modifications.American journal of physiology. Heart and circulatory physiology · 2010
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. 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

10 authors at 4 institutions in 1 country.

Dongqing WangEndocrinology Division, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD 21224, USA.
Xianmin Xia
Ying Liu
Alexis Oetting
Robert L Walker
Yuelin Zhu
Paul Meltzer
Philip A Cole
Yun-Bo Shi
Paul M Yen
Johns Hopkins Medicine · USNational Institutes of Health · USJohns Hopkins University · USNational Cancer Institute · US

Funding

Cancer Genomics Technology DevelopmentZIABC011091 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI MELTZER, PAUL S. · 2009 to 2025
$16.9M
Molecular mechanism of thyroid hormone receptor function during metamorphosisZIAHD001901 · NICHD · EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT · PI SHI, YUN-BO · 2009 to 2025
$13.1M
Regulation of Transcription by Thyroid Hormone ReceptorsR01DK069899 · NIDDK · JOHNS HOPKINS UNIVERSITY · PI YEN, PAUL M · 2005 to 2008
$1.2M
Intramural NIH HHSNIDDK NIH HHS 1R01 DK069899NIDDK NIH HHS R01 DK069899
6 · The paper itself

Abstract

Currently, little is known about histone modifications and molecular mechanisms of negatively regulated transcription. In pituitary cells, thyroid hormone (T(3)) decreased transcription, and surprisingly increased histone acetylation, of TSHalpha promoter. This increase was mediated directly by thyroid hormone receptor. Histone acetylation of H3K9 and H3K18 sites, two modifications usually associated with transcriptional activation, occur in negative regulation of TSHalpha promoter. T(3) also caused release of a corepressor complex composed of histone deacetylase 3 (HDAC3), transducin beta-like protein 1, and nuclear receptor coprepressor (NCoR)/ silencing mediator for retinoic and thyroid hormone receptor from TSHalpha promoter in chromatin immunoprecipitation assays. NCoR and HDAC3 overexpression selectively increased ligand-independent basal transcription. Two histone acetyltransferase inhibitors increased overall transcription but did not abrogate negative regulation or NCoR/HDAC3 complex release by T(3). Chromatin immunoprecipitation analyses of an endogenous positively regulated target gene showed increased histone acetylation and corepressor complex release with T(3) treatment. Finally, microarray analyses suggested there is a subset of negatively regulated genes with increased histone acetylation. These findings demonstrate the critical role of NCoR/HDAC3 complex in negative regulation of TSHalpha gene expression and show that similar complexes and overlapping epigenetic modifications can participate in both negative and positive transcriptional regulation.

Indexed as

AcetylationAnimalsCell LineChromatin ImmunoprecipitationGene Expression RegulationGlycoprotein Hormones, alpha SubunitHistonesOligonucleotide Array Sequence AnalysisPolymerase Chain ReactionPromoter Regions, GeneticProtein BindingRatsReceptors, Thyroid HormoneRepressor ProteinsTransducinTriiodothyronineGlycoprotein Hormones, alpha SubunitHistonesReceptors, Thyroid HormoneRepressor ProteinsTransducinTriiodothyronine

Identifiers

PMID19196836
PMCPMC2675953
OpenAlexW2153997114

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.