Evidence map›Paper›PMID 10655495›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2000

The sentrin-conjugating enzyme mUbc9 interacts with GLUT4 and GLUT1 glucose transporters and regulates transporter levels in skeletal muscle cells.

F Giorgino, O de Robertis, L Laviola, C Montrone, S Perrini, K C McCowen, R J Smith

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing 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

52 citing papers in PubMed, 163 citations in OpenAlex.

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  16. Identifying the pathways that control resource allocation in higher plants.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  17. Article
  18. Article
  19. Article
  20. Post-translational modifications of transporters.Pharmacology & therapeutics · 2018
    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

7 authors at 3 institutions in 2 countries.

F GiorginoIstituto di Clinica Medica, Endocrinologia e Malattie Metaboliche, University of Bari School of Medicine, I-70124 Bari, Italy. giorginf@tin.it
O de Robertis
L Laviola
C Montrone
S Perrini
K C McCowen
R J Smith
University of Bari Aldo Moro · ITHarvard University · USJoslin Diabetes Center · US

Funding

SPECIAL ASSAY COREP30DK036836 · NIDDK · JOSLIN DIABETES CENTER · PI ROHIT N. KULKARNI · 1986 to 2026
$50.5M
NIDDK NIH HHS DK36836NIDDK NIH HHS P30 DK036836
6 · The paper itself

Abstract

Glucose transport in insulin-regulated tissues is mediated by the GLUT4 and GLUT1 transporters. Using the yeast two-hybrid system, we have cloned the sentrin-conjugating enzyme mUbc9 as a protein that interacts with the GLUT4 COOH-terminal intracellular domain. The mUbc9 enzyme was found to bind directly to GLUT4 and GLUT1 through an 11-aa sequence common to the two transporters and to modify both transporters covalently by conjugation with the mUbc9 substrate, sentrin. Overexpression of mUbc9 in L6 skeletal muscle cells decreased GLUT1 transporter abundance 65%, resulting in decreased basal glucose transport. By contrast, mUbc9 overexpression increased GLUT4 abundance 8-fold, leading to enhanced transport stimulation by insulin. A dominant-negative mUbc9 mutant lacking catalytic activity had effects opposite to those of wild-type mUbc9. The regulation of GLUT4 and GLUT1 was specific, as evidenced by an absence of mUbc9 interaction with or regulation of the GLUT3 transporter isoform in L6 skeletal muscle cells. The mUbc9 sentrin-conjugating enzyme represents a novel regulator of GLUT1 and GLUT4 protein levels with potential importance as a determinant of basal and insulin-stimulated glucose uptake in normal and pathophysiological states.

Indexed as

Gene Expression RegulationMuscle ProteinsUbiquitin-Conjugating Enzymes3T3 CellsAmino Acid SequenceAnimalsBiological Transport, ActiveGlucoseGlucose Transporter Type 1Glucose Transporter Type 4InsulinLigasesMacromolecular SubstancesMiceMolecular Sequence DataMonosaccharide Transport ProteinsGlucoseGlucose Transporter Type 1Glucose Transporter Type 4InsulinLigasesMacromolecular SubstancesMonosaccharide Transport ProteinsMuscle ProteinsRecombinant Fusion ProteinsSlc2a1 protein, mouseSlc2a1 protein, ratSlc2a4 protein, mouseSlc2a4 protein, ratSUMO-1 ProteinUbiquitin-Conjugating EnzymesUbiquitin-Conjugating Enzyme UBC9Ubiquitins

Identifiers

PMID10655495
PMCPMC15543
OpenAlexW2056883829

What Socratic 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 Socratic graph.