Evidence map›Paper›PMID 30201609›Full record

ArticleThe Journal of biological chemistry2018

mTORC2 modulates the amplitude and duration of GFAT1 Ser-243 phosphorylation to maintain flux through the hexosamine pathway during starvation.

Joseph G Moloughney, Nicole M Vega-Cotto, Sharon Liu, Chadni Patel, Peter K Kim, Chang-Chih Wu, Danielle Albaciete, Cedric Magaway, Austin Chang, Swati Rajput and 3 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
1.4field-weighted citation impact, top 18% 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

31 citing papers in PubMed, 39 citations in OpenAlex.

  1. Article
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  5. Food for thought: Nutrient metabolism controlling early T cell development.BioEssays : news and reviews in molecular, cellular and developmental biology · 2025
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  6. Metabolic adaptations in prostate cancer.British journal of cancer · 2024
    Review
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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

13 authors at 1 institution in 1 country.

Joseph G MoloughneyFrom the Department of Biochemistry and Molecular Biology, Robert Wood Johnson Medical School, Rutgers, The State University of New Jersey, Piscataway, New Jersey 08854 and.
Nicole M Vega-CottoFrom the Department of Biochemistry and Molecular Biology, Robert Wood Johnson Medical School, Rutgers, The State University of New Jersey, Piscataway, New Jersey 08854 and.
Sharon LiuFrom the Department of Biochemistry and Molecular Biology, Robert Wood Johnson Medical School, Rutgers, The State University of New Jersey, Piscataway, New Jersey 08854 and.
Chadni PatelFrom the Department of Biochemistry and Molecular Biology, Robert Wood Johnson Medical School, Rutgers, The State University of New Jersey, Piscataway, New Jersey 08854 and.
Peter K KimFrom the Department of Biochemistry and Molecular Biology, Robert Wood Johnson Medical School, Rutgers, The State University of New Jersey, Piscataway, New Jersey 08854 and.
Chang-Chih WuFrom the Department of Biochemistry and Molecular Biology, Robert Wood Johnson Medical School, Rutgers, The State University of New Jersey, Piscataway, New Jersey 08854 and.
Danielle AlbacieteFrom the Department of Biochemistry and Molecular Biology, Robert Wood Johnson Medical School, Rutgers, The State University of New Jersey, Piscataway, New Jersey 08854 and.
Cedric MagawayFrom the Department of Biochemistry and Molecular Biology, Robert Wood Johnson Medical School, Rutgers, The State University of New Jersey, Piscataway, New Jersey 08854 and.
Austin ChangFrom the Department of Biochemistry and Molecular Biology, Robert Wood Johnson Medical School, Rutgers, The State University of New Jersey, Piscataway, New Jersey 08854 and.
Swati RajputFrom the Department of Biochemistry and Molecular Biology, Robert Wood Johnson Medical School, Rutgers, The State University of New Jersey, Piscataway, New Jersey 08854 and.
Xiaoyang SuDepartment of Medicine, Division of Endocrinology, Child Health Institute of New Jersey, Rutgers, The State University of New Jersey, New Brunswick, New Jersey 08901.
Guy WerlenFrom the Department of Biochemistry and Molecular Biology, Robert Wood Johnson Medical School, Rutgers, The State University of New Jersey, Piscataway, New Jersey 08854 and.
Estela JacintoFrom the Department of Biochemistry and Molecular Biology, Robert Wood Johnson Medical School, Rutgers, The State University of New Jersey, Piscataway, New Jersey 08854 and jacintes@rwjms.rutgers.edu.ORCID 0000-0001-7118-1759
Rutgers, The State University of New Jersey · US

Funding

TRANSCRIPTIONAL PROFILINGP30CA072720 · NCI · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI Tracie Saunders · 1997 to 2026
$94.5M
Inter-University Doctoral Degree:Puerto Rico to RutgersR25GM058389 · NIGMS · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI LANGER, JEROME ALAN, RIOS-VELAZQUEZ, CARLOS · 1998 to 2016
$3.0M
The Regulation of Cell Metabolism and Proliferation by mTOR complex 2R01GM079176 · NIGMS · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI JACINTO, ESTELA · 2008 to 2017
$2.8M
Cotranslational Functions of MTORR01CA154674 · NCI · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI JACINTO, ESTELA · 2012 to 2017
$1.8M
NCI NIH HHS P30 CA072720NCI NIH HHS R01 CA154674NIGMS NIH HHS R01 GM079176NIGMS NIH HHS R25 GM058389
6 · The paper itself

Abstract

The mechanistic target of rapamycin (mTOR) controls metabolic pathways in response to nutrients. Recently, we have shown that mTOR complex 2 (mTORC2) modulates the hexosamine biosynthetic pathway (HBP) by promoting the expression of the key enzyme of the HBP, glutamine:fructose-6-phosphate aminotransferase 1 (GFAT1). Here, we found that GFAT1 Ser-243 phosphorylation is also modulated in an mTORC2-dependent manner. In response to glutamine limitation, active mTORC2 prolongs the duration of Ser-243 phosphorylation, albeit at lower amplitude. Blocking glycolysis using 2-deoxyglucose robustly enhances Ser-243 phosphorylation, correlating with heightened mTORC2 activation, increased AMPK activity, and

Indexed as

AcetylglucosamineAnimalsBiosynthetic PathwaysGlutamine-Fructose-6-Phosphate Transaminase (Isomerizing)HexosaminesHumansMechanistic Target of Rapamycin Complex 2PhosphorylationSerineStarvationUridine Diphosphate N-AcetylglucosamineAcetylglucosamineGlutamine-Fructose-6-Phosphate Transaminase (Isomerizing)HexosaminesMechanistic Target of Rapamycin Complex 2SerineUridine Diphosphate N-AcetylglucosamineAkt PKBcell metabolismglutamineglutaminolysishexosamine biosynthesishexosamine biosynthetic pathwaymetabolismmTORmTOR complex (mTORC)nutrientsprotein phosphorylation

Identifiers

PMID30201609
PMCPMC6200946
OpenAlexW2889994107

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.