Evidence map›Paper›PMID 23580612›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2013

Regulation of Oct1/Pou2f1 transcription activity by O-GlcNAcylation.

Jinsuk Kang, Zuolian Shen, Jae-Min Lim, Hiroshi Handa, Lance Wells, Dean Tantin

Open access · greenAbstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
0.9field-weighted citation impact, top 25% 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

19 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
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  6. Review
  7. Characterization ofGenes · 2020
    Article
  8. Article
  9. Nutrient regulation of signaling and transcription.The Journal of biological chemistry · 2019
    Review
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  11. Article
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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

6 authors at 3 institutions in 2 countries.

Jinsuk KangDepartment of Pathology, University of Utah School of Medicine, Salt Lake City, UT 84112, USA.
Zuolian Shen
Jae-Min Lim
Hiroshi Handa
Lance Wells
Dean Tantin
University of Utah · USUniversity of Georgia · USTokyo Institute of Technology · JP

Funding

TR&D1: Stem Cell and Induced Pluripotent Stem Cell Resources (Pages 116-134)P41GM103490 · NIGMS · UNIVERSITY OF GEORGIA · PI PIERCE, J. MICHAEL · 2012 to 2018
$13.7M
ZINC DEFICIENCY &PROTEIN EXPRESSION IN RAT OLFACTORY BULBSP41RR018502 · NCRR · UNIVERSITY OF GEORGIA (UGA) · PI AZADI, PARASTOO · 2003 to 2011
$13.1M
Gene regulation of Oct1: implications of metabolism, stemness and cancerR21CA141009 · NCI · UNIVERSITY OF UTAH · PI TANTIN, DEAN · 2010 to 2011
$354k
NCI NIH HHS 1R21CA141009NCI NIH HHS R21 CA141009NCRR NIH HHS P41 RR018502NCRR NIH HHS P41RR018502NIGMS NIH HHS P41 GM103490
6 · The paper itself

Abstract

The Oct1 transcription factor is a potent regulator of stress responses, metabolism, and tumorigenicity. Although Oct1 is regulated by phosphorylation and ubiquitination, the presence and importance of other modifications is unknown. Here we show that Oct1 is modified by O-linked β-N-acetylglucosamine (O-GlcNAc) moieties. We map two sites of O-GlcNAcylation at positions T255 and S728 within human Oct1. Under anchorage-independent overgrowth conditions, Oct1 associates 3-fold more strongly with the Gadd45a promoter and mediates transcriptional repression. Increased binding correlates with quantitative reductions in Oct1 nuclear periphery-associated puncta, and a reduced association with lamin B1. The O-GlcNAc modification sites are important for both Gadd45a repression and anchorage-independent survival. In contrast to chronic overgrowth conditions, following acute nutrient starvation Oct1 mediates Gadd45a activation. The O-GlcNAc sites are also important for Gadd45a activation under these conditions. We also, for the first time, identify specific Oct1 ubiquitination sites. The findings suggest that Oct1 integrates metabolic and stress signals via O-GlcNAc modification to regulate target gene activity.

Indexed as

Transcriptional Activation3T3 CellsAcetylglucosamineAmino Acid SequenceAnimalsBinding SitesCell Cycle ProteinsEmbryo, MammalianFibroblastsGADD45 ProteinsGene Expression RegulationGreen Fluorescent ProteinsHeLa CellsHumansImmunoblottingMiceAcetylglucosamineCell Cycle ProteinsGADD45A protein, humanGADD45 ProteinsGreen Fluorescent ProteinsNuclear ProteinsPOU4F1 protein, humanTranscription Factor Brn-3AGadd45aLamin B

Identifiers

PMID23580612
PMCPMC3688745
OpenAlexW2144946280

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.