Evidence map›Paper›PMID 28178239›Full record

ArticleNature2017

EPRS is a critical mTORC1-S6K1 effector that influences adiposity in mice.

Abul Arif, Fulvia Terenzi, Alka A Potdar, Jie Jia, Jessica Sacks, Arnab China, Dalia Halawani, Kommireddy Vasu, Xiaoxia Li, J Mark Brown and 4 more

Abstract read
In one paragraph

Article in Nature, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 83 papers.

0numbers the graph read from it
0cells of the map it votes in
83citing papers in PubMed
6.4field-weighted citation impact, top 3% 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

83 citing papers in PubMed, 122 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. METTL1-mediated mOncogene · 2026
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  11. AKT-dependent nuclear localization of EPRS1 activates PARP1 in breast cancer cells.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. New Regulatory roles for Human Serum Amyloid A.International journal of research in oncology · 2024
    Article
  17. Article
  18. Article
  19. Review
  20. Multi-omic stratification of the missense variant cysteinome.bioRxiv : the preprint server for biology · 2023
    Article

23 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 4 institutions in 2 countries.

Abul ArifDepartment of Cellular and Molecular Medicine, Lerner Research Institute, Cleveland Clinic, Cleveland, Ohio 44195, USA.
Fulvia TerenziDepartment of Cellular and Molecular Medicine, Lerner Research Institute, Cleveland Clinic, Cleveland, Ohio 44195, USA.
Alka A PotdarF. Widjaja Foundation Inflammatory Bowel and Immunobiology Research Institute, Cedars-Sinai Medical Center, Los Angeles, California 90048, USA.
Jie JiaDepartment of Cellular and Molecular Medicine, Lerner Research Institute, Cleveland Clinic, Cleveland, Ohio 44195, USA.
Jessica SacksDepartment of Cellular and Molecular Medicine, Lerner Research Institute, Cleveland Clinic, Cleveland, Ohio 44195, USA.
Arnab ChinaDepartment of Cellular and Molecular Medicine, Lerner Research Institute, Cleveland Clinic, Cleveland, Ohio 44195, USA.
Dalia HalawaniDepartment of Cellular and Molecular Medicine, Lerner Research Institute, Cleveland Clinic, Cleveland, Ohio 44195, USA.
Kommireddy VasuDepartment of Cellular and Molecular Medicine, Lerner Research Institute, Cleveland Clinic, Cleveland, Ohio 44195, USA.
Xiaoxia LiDepartment of Immunology, Lerner Research Institute, Cleveland Clinic, Cleveland, Ohio 44195, USA.
J Mark BrownDepartment of Cellular and Molecular Medicine, Lerner Research Institute, Cleveland Clinic, Cleveland, Ohio 44195, USA.
Jie ChenDepartment of Cell and Developmental Biology, University of Illinois, Urbana, Illinois 61801, USA.
Sara C KozmaCatalan Institute of Oncology, ICO, Bellvitge Biomedical Research Institute, IDIBELL, Barcelona, Spain.
George ThomasCatalan Institute of Oncology, ICO, Bellvitge Biomedical Research Institute, IDIBELL, Barcelona, Spain.
Paul L FoxDepartment of Cellular and Molecular Medicine, Lerner Research Institute, Cleveland Clinic, Cleveland, Ohio 44195, USA.
Cleveland Clinic Lerner College of Medicine · USInstitut Català d'Oncologia · ESCedars-Sinai Medical Center · USUniversity of Illinois Urbana-Champaign · US

Funding

Vascular Cell function and AtherosclerosisP01HL029582 · NHLBI · CLEVELAND CLINIC LERNER COM-CWRU · PI FOX, PAUL L · 1985 to 2019
$32.0M
Structural Determinants Of Ceruloplasmin Inflammatory ActivityP01HL076491 · NHLBI · CLEVELAND CLINIC LERNER COM-CWRU · PI PLOW, EDWARD FRANKLIN · 2004 to 2019
$27.3M
Targeting 15-PGDH in Colon Cancer Prognosis, Prediction, Treatment and PreventionP50CA150964 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI MARKOWITZ, SANFORD D. · 2011 to 2022
$24.6M
mTOR Signaling in Skeletal MyogenesisR01AR048914 · NIAMS · UNIVERSITY OF ILLINOIS URBANA-CHAMPAIGN · PI CHEN, JIE · 2003 to 2019
$4.8M
Phospholipase D signalingR01GM089771 · NIGMS · UNIVERSITY OF ILLINOIS AT URBANA-CHAMPAIGN · PI CHEN, JIE · 2011 to 2025
$3.9M
A protein-directed RNA switch that regulates translationR01GM086430 · NIGMS · CLEVELAND CLINIC LERNER COM-CWRU · PI FOX, PAUL L · 2009 to 2016
$2.6M
The Function of rpL5 and rpL11 in induction of p53R01CA158768 · NCI · UNIVERSITY OF CINCINNATI · PI THOMAS, GEORGE · 2012 to 2017
$1.5M
Mechanisms and Regulation of Programmed Translational ReadthroughR01GM115476 · NIGMS · CLEVELAND CLINIC LERNER COM-CWRU · PI FOX, PAUL L · 2016 to 2019
$1.2M
NCI NIH HHS P50 CA150964NCI NIH HHS R01 CA158768NHLBI NIH HHS P01 HL029582NHLBI NIH HHS P01 HL076491NIAMS NIH HHS R01 AR048914NIGMS NIH HHS R01 GM086430NIGMS NIH HHS R01 GM089771NIGMS NIH HHS R01 GM115476
6 · The paper itself

Abstract

Metabolic pathways that contribute to adiposity and ageing are activated by the mammalian target of rapamycin complex 1 (mTORC1) and p70 ribosomal protein S6 kinase 1 (S6K1) axis. However, known mTORC1-S6K1 targets do not account for observed loss-of-function phenotypes, suggesting that there are additional downstream effectors of this pathway. Here we identify glutamyl-prolyl-tRNA synthetase (EPRS) as an mTORC1-S6K1 target that contributes to adiposity and ageing. Phosphorylation of EPRS at Ser999 by mTORC1-S6K1 induces its release from the aminoacyl tRNA multisynthetase complex, which is required for execution of noncanonical functions of EPRS beyond protein synthesis. To investigate the physiological function of EPRS phosphorylation, we generated Eprs knock-in mice bearing phospho-deficient Ser999-to-Ala (S999A) and phospho-mimetic (S999D) mutations. Homozygous S999A mice exhibited low body weight, reduced adipose tissue mass, and increased lifespan, similar to S6K1-deficient mice and mice with adipocyte-specific deficiency of raptor, an mTORC1 constituent. Substitution of the Eprs

Indexed as

AdiposityAdaptor Proteins, Signal TransducingAdipocytesAgingAmino Acyl-tRNA SynthetasesAnimalsBody WeightCell MembraneFatty AcidsFatty Acid Transport ProteinsFemaleInsulinLongevityMaleMechanistic Target of Rapamycin Complex 1MiceAdaptor Proteins, Signal TransducingAmino Acyl-tRNA SynthetasesFatty AcidsFatty Acid Transport Proteinsglutamyl-prolyl-tRNA synthetaseInsulinMechanistic Target of Rapamycin Complex 1Multiprotein ComplexesPhosphoserineRegulatory-Associated Protein of mTORRibosomal Protein S6 Kinases, 90-kDaRps6ka1 protein, mouseRptor protein, mouseSlc27a1 protein, mouseTOR Serine-Threonine Kinases

Identifiers

PMID28178239
PMCPMC5480610
OpenAlexW2586533164

What OpenQuestion holds

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Registered trials

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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.