Evidence map›Paper›PMID 24076017›Full record

ReviewBiochimica et biophysica acta2013

O-GlcNAcylation at promoters, nutrient sensors, and transcriptional regulation.

Brian A Lewis

Abstract readReview
In one paragraph

Review in Biochimica et biophysica acta, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
–field-weighted citation impact
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

18 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. International journal of molecular sciences · 2019
    Article
  5. Targeted covalent inhibition of O-GlcNAc transferase in cells.Chemical communications (Cambridge, England) · 2019
    Article
  6. 'Molecules (Basel, Switzerland) · 2018
    Review
  7. Article
  8. Article
  9. The pol II CTD: new twists in the tail.Nature structural & molecular biology · 2016
    Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Review
  16. 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
  17. Article
  18. 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

1 author.

Brian A LewisMetabolism Branch, CCR/NCI/NIH, 9000 Rockville Pike, Bethesda, MD 20892, USA. Electronic address: lewisbri@mail.nih.gov.

Funding

Regulation of Transcription Initiation and Elongation by O-GlcNAcylation EnzymesZIABC011223 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI LEWIS, BRIAN · 2009 to 2016
$3.8M
Intramural NIH HHS ZIA BC011223
6 · The paper itself

Abstract

Post-translational modifications play important roles in transcriptional regulation. Among the less understood PTMs is O-GlcNAcylation. Nevertheless, O-GlcNAcylation in the nucleus is found on hundreds of transcription factors and coactivators and is often found in a mutually exclusive ying-yang relationship with phosphorylation. O-GlcNAcylation also links cellular metabolism directly to the proteome, serving as a conduit of metabolic information to the nucleus. This review serves as a brief introduction to O-GlcNAcylation, emphasizing its important thematic roles in transcriptional regulation, and highlights several recent and important additions to the literature that illustrate the connections between O-GlcNAc and transcription.

Indexed as

Gene Expression RegulationPromoter Regions, GeneticTranscription, GeneticAcetylglucosamineHumansRNA Polymerase IIAcetylglucosamineRNA Polymerase IINutrient sensorO-GlcNAcRNA polymerase IITranscription

Identifiers

PMID24076017
PMCPMC3833346

What OpenQuestion holds

Textmetadata
LicenceTDM
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.