Evidence map›Paper›PMID 16966374›Full record

ArticleMolecular and cellular biology2006

O-GlcNAc integrates the proteasome and transcriptome to regulate nuclear hormone receptors.

Damon B Bowe, Andrea Sadlonova, Clifford A Toleman, Zdenek Novak, Yong Hu, Ping Huang, Shibani Mukherjee, Timothy Whitsett, Andra R Frost, Andrew J Paterson and 1 more

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular biology, 2006. 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
2.0field-weighted citation impact, top 14% 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, 38 citations in OpenAlex.

  1. Review
  2. Article
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  5. Article
  6. O-GlcNAcylation in women's cancers: breast, endometrial and ovarian.Journal of bioenergetics and biomembranes · 2018
    Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Post-translational modification of cardiac proteasomes: functional delineation enabled by proteomics.American journal of physiology. Heart and circulatory physiology · 2012
    Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. Review
  19. Review
  20. Increased O-GlcNAc causes disrupted lens fiber cell differentiation and cataracts.Biochemical and biophysical research communications · 2009
    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

11 authors at 3 institutions in 1 country.

Damon B BoweDepartment of Pharmacology and Toxicology, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
Andrea Sadlonova
Clifford A Toleman
Zdenek Novak
Yong Hu
Ping Huang
Shibani Mukherjee
Timothy Whitsett
Andra R Frost
Andrew J Paterson
Jeffrey E Kudlow
University of Alabama at Birmingham · USChildren's of Alabama · USUniversity of California, San Diego · US

Funding

O-Glycosylation in Breast CancerR01DK043652 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI PATERSON, ANDREW JAMES · 1991 to 2010
$2.6M
NIDDK NIH HHS 2R01DK43652-14A1NIDDK NIH HHS R01 DK043652
6 · The paper itself

Abstract

Mechanisms controlling nuclear hormone receptors are a central question to mammalian developmental and disease processes. Herein, we show that a subtle increase in O-GlcNAc levels inhibits activation of nuclear hormone receptors. In vivo, increased levels of O-GlcNAc impair estrogen receptor activation and cause a decrease in mammary ductal side-branching morphogenesis associated with loss of progesterone receptors. Increased O-GlcNAc levels suppress transcriptional expression of coactivators and of the nuclear hormone receptors themselves. Surprisingly, increased O-GlcNAc levels are also associated with increased transcription of genes encoding corepressor proteins NCoR and SMRT. The association of the enzyme O-GlcNAc transferase with these corepressors contributes to specific regulation of nuclear hormone receptors by O-GlcNAc. Overall, transcriptional inhibition is related to the integrated effect of O-GlcNAc by direct modification of critical elements of the transcriptome and indirectly through O-GlcNAc modification of the proteasome.

Indexed as

Gene Expression RegulationTranscription, GeneticAnimalsCell Line, TumorHumansMammary Glands, HumanMiceMice, TransgenicModels, BiologicalN-AcetylglucosaminyltransferasesNuclear ProteinsNuclear Receptor Co-Repressor 1Proteasome Endopeptidase ComplexReceptors, Cytoplasmic and NuclearRepressor ProteinsTransfectionN-AcetylglucosaminyltransferasesNCOR1 protein, humanNcor1 protein, mouseNuclear ProteinsNuclear Receptor Co-Repressor 1O-GlcNAc transferaseProteasome Endopeptidase ComplexReceptors, Cytoplasmic and NuclearRepressor Proteins

Identifiers

PMID16966374
PMCPMC1636782
OpenAlexW2141948569

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.