Evidence map›Paper›PMID 29386567›Full record

ArticleScientific reports2018

MGAT1 and Complex N-Glycans Regulate ERK Signaling During Spermatogenesis.

Barnali Biswas, Frank Batista, Subha Sundaram, Pamela Stanley

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

13 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Dysregulation of N-glycosylation byInternational journal of biological sciences · 2025
    Article
  3. Review
  4. Article
  5. Deletion ofFrontiers in cell and developmental biology · 2024
    Article
  6. Article
  7. Review
  8. Article
  9. Observational
  10. Article
  11. 3D Structure and Function of Glycosyltransferases Involved inInternational journal of molecular sciences · 2020
    Review
  12. Transgenic Rescue of Spermatogenesis in Males WithFrontiers in cell and developmental biology · 2020
    Article
  13. Roles for Golgi Glycans in Oogenesis and Spermatogenesis.Frontiers in cell and developmental biology · 2019
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 1 institution in 2 countries.

Barnali BiswasDepartment of Cell Biology, Albert Einstein College of Medicine, New York, NY, 10461, USA.
Frank BatistaDepartment of Cell Biology, Albert Einstein College of Medicine, New York, NY, 10461, USA.
Subha SundaramDepartment of Cell Biology, Albert Einstein College of Medicine, New York, NY, 10461, USA.
Pamela StanleyDepartment of Cell Biology, Albert Einstein College of Medicine, New York, NY, 10461, USA. pamela.stanley@einstein.yu.edu.ORCID http://orcid.org/0000-0001-5704-3747
Albert Einstein College of Medicine · US

Funding

Lectin Resistant Tumor Cells and Functional GlycomicsR01GM105399 · NIGMS · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI STANLEY, PAMELA M · 2013 to 2022
$3.6M
High-speed/resolution whole slide scanner supported by two core facilitiesS10OD019961 · OD · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI CONDEELIS, JOHN S · 2015 to 2015
$326k
NIGMS NIH HHS R01 GM105399NIH HHS S10 OD019961
6 · The paper itself

Abstract

Mechanisms that regulate spermatogenesis in mice are important to define as they often apply to fertility in man. We previously showed that conditional deletion of the mouse Mgat1 gene (Mgat1 cKO) in spermatogonia causes a germ-cell autonomous defect leading to infertility. MGAT1 is the N-acetylglucosaminyltransferase (GlcNAcT-I) that initiates the synthesis of complex N-glycans. Mechanistic bases of MGAT1 loss were investigated in germ cells from 22- and 23-day males, before any changes in germ cell morphology were apparent. Gene expression changes induced by deletion of Mgat1 were determined using the Affymetrix gene chip Mouse Mogene 2.0 ST array, and relationships were investigated by bioinformatics including Gene Ontology (GO), Ingenuity Pathway Analysis (IPA), and Gene Set Enrichment Analysis (GSEA). The loss of complex N-glycans promoted the premature up-regulation of genes normally expressed later in spermatogenesis and spermiogenesis, and IPA and GSEA implicated ERK signaling. EGFR and PDGFRA transcripts and ERK1/2 signaling were reduced in 22-day Mgat1 cKO germ cells. Basigin, a germ cell target of MGAT1, activated ERK1/2 in CHO cells, but not in a Lec1 CHO mutant that lacks MGAT1 and complex N-glycans. Thus, MGAT1 is required to regulate ERK1/2 signaling during spermatogenesis, potentially via different mechanisms.

Indexed as

MAP Kinase Signaling SystemSpermatogenesisAcyltransferasesAnimalsBasiginCells, CulturedCHO CellsCricetinaeCricetulusErbB ReceptorsMaleMiceMitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3N-AcetylglucosaminyltransferasesPolysaccharidesAcyltransferasesBasiginErbB ReceptorsMGAT1 protein, mouseMitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3N-AcetylglucosaminyltransferasesPolysaccharidesReceptor, Platelet-Derived Growth Factor alpha

Identifiers

PMID29386567
PMCPMC5792458
OpenAlexW2805357125

What OpenQuestion 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 OpenQuestion graph.