Evidence map›Paper›PMID 24616106›Full record

ArticleThe Journal of biological chemistry2014

O-GlcNAc transferase is critical for transducin-like enhancer of split (TLE)-mediated repression of canonical Wnt signaling.

Jing Wu, Damon B Bowe, Andrea Sadlonova, Thomas R Whisenhunt, Yong Hu, Anil K Rustgi, Yongzhan Nie, Andrew J Paterson, Xiaoyong Yang

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.4field-weighted citation impact, top 36% 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

11 citing papers in PubMed, 16 citations in OpenAlex.

  1. Inhibition ofeLife · 2024
    Article
  2. Inhibition ofbioRxiv : the preprint server for biology · 2024
    Article
  3. The world journal of men's health · 2023
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. The Wnt Transcriptional Switch: TLE Removal or Inactivation?BioEssays : news and reviews in molecular, cellular and developmental biology · 2018
    Review
  10. Proteomic analysis reveals O-GlcNAc modification on proteins with key regulatory functions inProceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  11. 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

9 authors at 5 institutions in 2 countries.

Jing WuCenter for Mitochondrial Biology and Medicine, the Key Laboratory of Biomedical Information Engineering of Ministry of Education, School of Life Science and Technology and Frontier Institute of Science and Technology, Xi'an Jiaotong University, Xi'an 710049, China; Section of Comparative Medicine and Department of Cellular and Molecular Physiology, Yale University School of Medicine, New Haven, Connecticut 06519.
Damon B BoweDivision of Endocrinology and Metabolism, University of Alabama at Birmingham, Birmingham, Alabama 35294.
Andrea SadlonovaDepartment of Pathology and Laboratory Medicine, Emory University, Atlanta, Georgia 30322.
Thomas R WhisenhuntDivision of Endocrinology and Metabolism, University of Alabama at Birmingham, Birmingham, Alabama 35294.
Yong HuDivision of Endocrinology and Metabolism, University of Alabama at Birmingham, Birmingham, Alabama 35294.
Anil K RustgiDepartment of Medicine (GI) and Genetics, Abramson Cancer Center, 600 CRB, University of Pennsylvania, Philadelphia, Pennsylvania 19104.
Yongzhan NieState Key Laboratory of Cancer Biology and Xijing Hospital of Digestive Diseases, Fourth Military Medical University, 127 West Changle Road, Xi'an, Shaanxi 710032, China.
Andrew J PatersonDivision of Endocrinology and Metabolism, University of Alabama at Birmingham, Birmingham, Alabama 35294.
Xiaoyong YangSection of Comparative Medicine and Department of Cellular and Molecular Physiology, Yale University School of Medicine, New Haven, Connecticut 06519. Electronic address: xiaoyong.yang@yale.edu.
University of Alabama at Birmingham · USYale University · USAir Force Medical University · CNEmory University · USUniversity of Pennsylvania · US

Funding

Yale Liver CenterP30DK034989 · NIDDK · YALE UNIVERSITY · PI YASUKO IWAKIRI · 1986 to 2026
$31.1M
Translational CoreP01DK057751 · NIDDK · YALE UNIVERSITY · PI NATHANSON, MICHAEL H · 2001 to 2020
$25.6M
O-GlcNAc Modification in Metabolic HomeostasisR01DK089098 · NIDDK · YALE UNIVERSITY · PI YANG, XIAOYONG · 2010 to 2021
$3.0M
O-Glycosylation in Breast CancerR01DK043652 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI PATERSON, ANDREW JAMES · 1991 to 2010
$2.6M
NIDDK NIH HHS DK043652NIDDK NIH HHS P01 DK057751NIDDK NIH HHS P30 DK034989NIDDK NIH HHS R01 DK043652NIDDK NIH HHS R01 DK089098
6 · The paper itself

Abstract

The Drosophila Groucho protein and its mammalian orthologues the transducin-like enhancers of split (TLEs) are critical transcriptional corepressors that repress Wnt and other signaling pathways. Although it is known that Groucho/TLEs are recruited to target genes by pathway-specific transcription factors, molecular events after the corepressor recruitment are largely unclear. We report that association of TLEs with O-GlcNAc transferase, an enzyme that catalyzes posttranslational modification of proteins by O-linked N-acetylglucosamine, is essential for TLE-mediated transcriptional repression. Removal of O-GlcNAc from Wnt-responsive gene promoters is critical for gene activation from Wnt-responsive promoters. Thus, these studies identify a molecular mechanism by which Groucho/TLEs repress gene transcription and provide a model whereby O-GlcNAc may control distinct intracellular signaling pathways.

Indexed as

Signal TransductionWnt Signaling PathwayAnimalsBase SequenceChromatin ImmunoprecipitationDNA PrimersDrosophilaHumansN-AcetylglucosaminyltransferasesReal-Time Polymerase Chain ReactionTransducinDNA PrimersN-AcetylglucosaminyltransferasesO-GlcNAc transferaseTransducinGene SilencingGroucho/TLEO-GlcNAcOGTSignal TransductionTranscription RepressorWnt Pathway

Identifiers

PMID24616106
PMCPMC4002120
OpenAlexW2069687733

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.