Evidence map›Paper›PMID 22371499›Full record

ArticleThe Journal of biological chemistry2012

O-GlcNAc transferase is involved in glucocorticoid receptor-mediated transrepression.

Min-Dian Li, Hai-Bin Ruan, Jay P Singh, Lin Zhao, Tingting Zhao, Sascha Azarhoush, Jing Wu, Ronald M Evans, Xiaoyong Yang

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

25 citing papers in PubMed, 45 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Review
  6. Review
  7. Article
  8. Review
  9. Article
  10. Review
  11. Protein O-GlcNAcylation: emerging mechanisms and functions.Nature reviews. Molecular cell biology · 2017
    Review
  12. Article
  13. Review
  14. Review
  15. OGT-mediated O-GlcNAcylation promotes NF-κB activation and inflammation in acute pancreatitis.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2015
    Article
  16. Article
  17. Review
  18. Targeted placental deletion of OGT recapitulates the prenatal stress phenotype including hypothalamic mitochondrial dysfunction.Proceedings of the National Academy of Sciences of the United States of America · 2014
    Article
  19. Article
  20. O-GlcNAc: A Bittersweet Switch in Liver.Frontiers in endocrinology · 2014
    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

9 authors at 2 institutions in 3 countries.

Min-Dian LiDepartment of Cellular and Molecular Physiology, Section of Comparative Medicine and Program in Integrative Cell Signaling and Neurobiology of Metabolism, Yale University School of Medicine, New Haven, Connecticut 06520, USA.
Hai-Bin Ruan
Jay P Singh
Lin Zhao
Tingting Zhao
Sascha Azarhoush
Jing Wu
Ronald M Evans
Xiaoyong Yang
Yale University · USSalk Institute for Biological Studies · US

Funding

Viral Vector Core (VVC)P30CA014195 · NCI · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI Ye Zheng · 1985 to 2026
$82.8M
ProteomicsU19DK062434 · NIDDK · UNIVERSITY OF TEXAS SW MED CTR/DALLAS · PI MOORE, DAVID D · 2002 to 2011
$37.4M
Spatial Regulation of Developmental Gene ExpressionR01HL105278 · NHLBI · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI EVANS, RONALD M · 2011 to 2019
$4.0M
O-GlcNAc Modification in Metabolic HomeostasisR01DK089098 · NIDDK · YALE UNIVERSITY · PI YANG, XIAOYONG · 2010 to 2021
$3.0M
Glucocorticoid Regulation of NF-kB Function by O-GlcNAcF32DK066971 · NIDDK · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI YANG, XIAOYONG · 2004 to 2006
$149k
Howard Hughes Medical InstituteNCI NIH HHS CA014195-38NCI NIH HHS P30 CA014195NHLBI NIH HHS HL105278NHLBI NIH HHS R01 HL105278NIDDK NIH HHS DK062434NIDDK NIH HHS DK066971NIDDK NIH HHS DK089098NIDDK NIH HHS F32 DK066971NIDDK NIH HHS R01 DK089098NIDDK NIH HHS U19 DK062434
6 · The paper itself

Abstract

Recruitment of O-GlcNAc transferase (OGT) to promoters plays an important role in gene repression. Glucocorticoid signaling represses the transcriptional activities of NF-κB and AP-1 through direct binding, yet the molecular mechanisms remain to be elucidated. Here we report that OGT is an important component of GR-mediated transrepression. OGT associates with ligand-bound GR in a multi-protein repression complex. Overexpression of OGT potentiates the GR transrepression pathway, whereas depletion of endogenous OGT by RNA interference abolishes the repression. The recruitment of OGT by GR leads to increased O-GlcNAcylation and decreased phosphorylation of RNA polymerase II on target genes. Functionally, overexpression of OGT enhances glucocorticoid-induced apoptosis in resistant cell lines while knockdown of OGT prevents sensitive cell lines from apoptosis. These studies identify a molecular mechanism of GR transrepression, and highlight the function of O-GlcNAc in hormone signaling.

Indexed as

AcetylglucosamineAnti-Inflammatory AgentsApoptosisCell Line, TumorDrug DesignGene Expression Regulation, EnzymologicHEK293 CellsHumansHydrocortisoneLung NeoplasmsN-AcetylglucosaminyltransferasesNF-kappa BNuclear Receptor Coactivator 2Receptors, Cytoplasmic and NuclearReceptors, GlucocorticoidRNA Polymerase IIAcetylglucosamineAnti-Inflammatory AgentsHydrocortisoneN-AcetylglucosaminyltransferasesNCOA2 protein, humanNF-kappa BNuclear Receptor Coactivator 2O-GlcNAc transferaseReceptors, Cytoplasmic and NuclearReceptors, GlucocorticoidRNA Polymerase II

Identifiers

PMID22371499
PMCPMC3339970
OpenAlexW2068810487

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.