Evidence map›Paper›PMID 35304331›Full record

ArticleMolecular metabolism2022

A novel role for GalNAc-T2 dependent glycosylation in energy homeostasis.

Cristy R C Verzijl, Federico Oldoni, Natalia Loaiza, Justina C Wolters, Antoine Rimbert, E Tian, Weiming Yang, Dicky Struik, Marieke Smit, Niels J Kloosterhuis and 9 more

Open access · goldAbstract read
In one paragraph

Article in Molecular metabolism, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.9field-weighted citation impact, top 30% 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

7 citing papers in PubMed, 11 citations in OpenAlex.

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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

19 authors at 7 institutions in 3 countries.

Cristy R C VerzijlDepartment of Pediatrics, University of Groningen, University Medical Center Groningen, Groningen, the Netherlands.
Federico OldoniDepartment of Molecular Genetics, University of Texas Southwestern Medical Center, Dallas, TX, United States.
Natalia LoaizaDepartment of Pediatrics, University of Groningen, University Medical Center Groningen, Groningen, the Netherlands.
Justina C WoltersDepartment of Pediatrics, University of Groningen, University Medical Center Groningen, Groningen, the Netherlands.
Antoine RimbertNantes Université, CNRS, INSERM, l'institut du thorax, F-44000, Nantes, France.
E TianDevelopmental Glycobiology Section, NIDCR, National Institutes of Health, Bethesda, MD, United States.
Weiming YangSection on Biological Chemistry, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MD, United States.
Dicky StruikDepartment of Pediatrics, University of Groningen, University Medical Center Groningen, Groningen, the Netherlands.
Marieke SmitDepartment of Pediatrics, University of Groningen, University Medical Center Groningen, Groningen, the Netherlands.
Niels J KloosterhuisDepartment of Pediatrics, University of Groningen, University Medical Center Groningen, Groningen, the Netherlands.
Amy J FernandezDepartment of Biophysics and Biophysical Chemistry, Johns Hopkins University School of Medicine, Baltimore, MD, United States.
Nadine L SamaraStructural Biochemistry Unit, National Institutes of Health, Bethesda, MD, United States; Developmental Glycobiology Section, NIDCR, National Institutes of Health, Bethesda, MD, United States.
Kelly G Ten HagenDevelopmental Glycobiology Section, NIDCR, National Institutes of Health, Bethesda, MD, United States.
Kruti DalalSection on Biological Chemistry, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MD, United States.
Aliona ChernishSection on Biological Chemistry, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MD, United States.
Peggy McCluggageSection on Biological Chemistry, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MD, United States.
Lawrence A TabakSection on Biological Chemistry, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MD, United States.
Johan W JonkerDepartment of Pediatrics, University of Groningen, University Medical Center Groningen, Groningen, the Netherlands.
Jan Albert KuivenhovenDepartment of Pediatrics, University of Groningen, University Medical Center Groningen, Groningen, the Netherlands. Electronic address: j.a.kuivenhoven@umcg.nl.
National Institutes of Health · USUniversity of Groningen · NLUniversity Medical Center Groningen · NLNational Institute of Dental and Craniofacial Research · USInserm · FRJohns Hopkins Medicine · USThe University of Texas Southwestern Medical Center · US

Funding

Role of O-glycosylation in Animal DevelopmentZIADE000713 · NIDCR · NATIONAL INSTITUTE OF DENTAL & CRANIOFACIAL RESEARCH · PI TEN HAGEN, KELLY G · 2009 to 2025
$30.6M
Structure and Function of UDP-GalNAc:polypeptide alpha-GalNAc transferasesZIADE000739 · NIDCR · NATIONAL INSTITUTE OF DENTAL & CRANIOFACIAL RESEARCH · PI TABAK, LAWRENCE A. · 2012 to 2025
$12.9M
Role of O-glycosylation in Animal DevelopmentZ01DE000713 · NIDCR · NATIONAL INSTITUTE OF DENTAL & CRANIOFACIAL RESEARCH · PI TEN HAGEN, KELLY G · 2006 to 2008
$2.0M
Intramural NIH HHS Z01 DE000713Intramural NIH HHS ZIA DE000739Medical Research Council MC_PC_17228Medical Research Council MC_QA137853
6 · The paper itself

Abstract

objectiveGALNT2, encoding polypeptide N-acetylgalactosaminyltransferase 2 (GalNAc-T2), was initially discovered as a regulator of high-density lipoprotein metabolism. GalNAc-T2 is known to exert these effects through post-translational modification, i.e., O-linked glycosylation of secreted proteins with established roles in plasma lipid metabolism. It has recently become clear that loss of GALNT2 in rodents, cattle, nonhuman primates, and humans should be regarded as a novel congenital disorder of glycosylation that affects development and body weight. The role of GALNT2 in metabolic abnormalities other than plasma lipids, including insulin sensitivity and energy homeostasis, is poorly understood.

methodsGWAS data from the UK Biobank was used to study variation in the GALNT2 locus beyond changes in high-density lipoprotein metabolism. Experimental data were obtained through studies in Galnt2

resultsFirst, we uncovered associations between GALNT2 gene variation, adiposity, and body mass index in humans. In mice, we identify the insulin receptor as a novel substrate of GalNAc-T2 and demonstrate that Galnt2

conclusionsThis study identifies a novel role for GALNT2 in energy homeostasis, and our findings suggest that the local effects of GalNAc-T2 are mediated through posttranslational modification of the insulin receptor.

Indexed as

Lipoproteins, HDLReceptor, InsulinAnimalsCattleGlycosylationHomeostasisMiceN-AcetylgalactosaminyltransferasesPolypeptide N-acetylgalactosaminyltransferaseLipoproteins, HDLN-AcetylgalactosaminyltransferasesPolypeptide N-acetylgalactosaminyltransferaseReceptor, InsulinAdipose tissueEnergy metabolismGenetic disorderGlycosylationInsulin signaling

Identifiers

PMID35304331
PMCPMC9019398
OpenAlexW4220869025

What Socratic holds

Textmetadata
LicenceCC BY
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.