Evidence map›Paper›PMID 22959271›Full record

ArticleMolecular cell2012

The G protein-coupled taste receptor T1R1/T1R3 regulates mTORC1 and autophagy.

Eric M Wauson, Elma Zaganjor, A-Young Lee, Marcy L Guerra, Anwesha B Ghosh, Angie L Bookout, Chris P Chambers, Arif Jivan, Kathleen McGlynn, Michele R Hutchison and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Molecular cell, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 100 papers.

0numbers the graph read from it
0cells of the map it votes in
100citing papers in PubMed
10.7field-weighted citation impact, top 1% 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

100 citing papers in PubMed, 187 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Animal amino acid sensor - A review.Animal bioscience · 2025
    Article
  9. Bitter taste receptors.Chemical senses · 2025
    Review
  10. Article
  11. L-Glutamate Regulates Npy via the mGluR4-CaInternational journal of molecular sciences · 2024
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. New Insights into the Regulation of mTOR Signaling via CaInternational journal of molecular sciences · 2023
    Review
  20. Review

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

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

12 authors at 1 institution in 1 country.

Eric M WausonDepartment of Pharmacology, University of Texas Southwestern Medical Center, Dallas, Dallas, TX 75390-9041, USA.
Elma Zaganjor
A-Young Lee
Marcy L Guerra
Anwesha B Ghosh
Angie L Bookout
Chris P Chambers
Arif Jivan
Kathleen McGlynn
Michele R Hutchison
Ralph J Deberardinis
Melanie H Cobb
The University of Texas Southwestern Medical Center · US

Funding

UT Southwestern Medical Center Simmons Comprehensive Cancer CenterP30CA142543 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI Sandi Leigh Pruitt · 2010 to 2026
$53.7M
MECHANISMS OF DRUG ACTION AND DISPOSITIONT32GM007062 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI MANGELSDORF, DAVID J · 1985 to 2020
$7.4M
Insulin-Regulated MAP Kinase PathwaysR37DK034128 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI COBB, MELANIE H. · 2007 to 2016
$5.1M
MAP Kinse in Islet FunctionR01DK055310 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI COBB, MELANIE H. · 1998 to 2014
$3.4M
METABOLIC REGULATORS OF TUMOR CELL GROWTHR01CA157996 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI DEBERARDINIS, RALPH J · 2011 to 2017
$2.2M
NCI NIH HHS P30 CA142543NCI NIH HHS R01 CA157996NIDDK NIH HHS R01 DK055310NIDDK NIH HHS R01 DK55310NIDDK NIH HHS R37 DK034128NIDDK NIH HHS R37 DK34128NIGMS NIH HHS 5-T32 GM007062NIGMS NIH HHS T32 GM007062
6 · The paper itself

Abstract

Cells continually assess their energy and nutrient state to maintain growth and survival and engage necessary homeostatic mechanisms. Cell-autonomous responses to the fed state require the surveillance of the availability of amino acids and other nutrients. The mammalian target of rapamycin complex 1 (mTORC1) integrates information on nutrient and amino acid availability to support protein synthesis and cell growth. We identify the G protein-coupled receptor (GPCR) T1R1/T1R3 as a direct sensor of the fed state and amino acid availability. Knocking down this receptor, which is found in most tissues, reduces the ability of amino acids to signal to mTORC1. Interfering with this receptor alters localization of mTORC1, downregulates expression of pathway inhibitors, upregulates key amino acid transporters, blocks translation initiation, and induces autophagy. These findings reveal a mechanism for communicating amino acid availability through a GPCR to mTORC1 in mammals.

Indexed as

AutophagyAmino AcidsAnimalsDown-RegulationExtracellular Signal-Regulated MAP KinasesInsulinInsulin-Secreting CellsMechanistic Target of Rapamycin Complex 1MiceMice, KnockoutMultiprotein ComplexesProtein BiosynthesisProteinsReceptors, G-Protein-CoupledRNA InterferenceRNA, Small InterferingAmino AcidsExtracellular Signal-Regulated MAP KinasesInsulinMechanistic Target of Rapamycin Complex 1Multiprotein ComplexesProteinsReceptors, G-Protein-CoupledRNA, Small Interferingtaste receptors, type 1TOR Serine-Threonine Kinases

Identifiers

PMID22959271
PMCPMC3749915
OpenAlexW2020179522

What OpenQuestion holds

Textmetadata
LicenceTDM
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.