Evidence map›Paper›PMID 18304804›Full record

ArticleThe Journal of steroid biochemistry and molecular biology2008

Differential recruitment of glucocorticoid receptor phospho-isoforms to glucocorticoid-induced genes.

Raymond D Blind, Michael J Garabedian

Open access · greenAbstract read
In one paragraph

Article in The Journal of steroid biochemistry and molecular biology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 70 papers.

0numbers the graph read from it
0cells of the map it votes in
70citing papers in PubMed
8.2field-weighted citation impact, top 2% 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

70 citing papers in PubMed, 119 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Crosstalk between p38 MAPK and GR Signaling.International journal of molecular sciences · 2022
    Review
  10. Article
  11. Review
  12. International journal of molecular medicine · 2021
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. The Glucocorticoid Receptor Is a Critical Regulator of HIV Latency in Human Microglial Cells.Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology · 2019
    Article
  20. Review

10 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

2 authors at 1 institution in 1 country.

Raymond D BlindDepartment of Microbiology, NYU Cancer Institute, NYU School of Medicine, 550 First Avenue, New York, NY 10016, United States.
Michael J Garabedian
New York University · US

Funding

REGULATION OF ANDROGEN RECEPTOR ACTIVITY IN THE PROSTATER01DK058024 · NIDDK · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI GARABEDIAN, MICHAEL J · 2000 to 2003
$1.1M
REGULATION OF GLUCOCORTICOID RECEPTOR BY PHOSPHORYLATIONR01DK054836 · NIDDK · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI GARABEDIAN, MICHAEL J · 1999 to 2002
$952k
NIDDK NIH HHS DK54836NIDDK NIH HHS R01 DK054836NIDDK NIH HHS R01 DK058024
6 · The paper itself

Abstract

The human glucocorticoid receptor (GR) is phosphorylated on its N-terminus at three major sites (S203, S211 and S226) within activation function 1 (AF1). Although GR has been shown to assemble at glucocorticoid responsive elements (GREs) in the presence of hormone, the timing and specificity of GR phospho-isoform recruitment to receptor target genes has not been established. Using chromatin immunoprecipitation (ChIP) and GR phosphorylation site-specific antibodies, we examined GR phospho-isoform recruitment to several glucocorticoid-induced genes including tyrosine aminotransferase (tat) and sulfonyltransferase-1A1 (sult) in rat hepatoma cells, and the glucocorticoid-induced leucine zipper (gilz) gene in human U2OS cells. GR P-S211 and GR P-S226 isoforms were efficiently recruited to the tat, sult and gilz GREs in a hormone-dependent manner. In contrast, the GR P-S203 isoform displayed no significant recruitment to any GREs of the genes analyzed, consistent with its lack of nuclear accumulation. Interestingly, the kinetics of GR P-S211 and GR P-S226 recruitment differed among genes. Our findings indicate that GR phospho-isoforms selectively occupy GR target genes, and suggests gene specific requirements for GR phosphorylation in receptor-dependent transcriptional activation.

Indexed as

AnimalsArylsulfotransferaseBase SequenceBinding SitesCell Line, TumorDexamethasoneDNADNA PrimersHumansPhosphorylationProtein IsoformsRatsReceptors, GlucocorticoidRNA, MessengerTranscriptional ActivationTranscription FactorsArylsulfotransferaseDexamethasoneDNADNA PrimersProtein IsoformsReceptors, GlucocorticoidRNA, MessengerTranscription FactorsTSC22D3 protein, humanTyrosine Transaminase

Identifiers

PMID18304804
PMCPMC2699583
OpenAlexW1990118125

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.