Evidence map›Paper›PMID 25002487›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2014

TOR complex 2-Ypk1 signaling is an essential positive regulator of the general amino acid control response and autophagy.

Ariadne Vlahakis, Martin Graef, Jodi Nunnari, Ted Powers

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 2 pooled it
4.7field-weighted citation impact, top 5% 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

29 citing papers in PubMed, 2 syntheses or guidelines pooled it, 68 citations in OpenAlex.

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  10. mTORC2: a multifaceted regulator of autophagy.Cell communication and signaling : CCS · 2023
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  20. Express yourself: how PP2A-B55Current genetics · 2018
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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

4 authors at 1 institution in 1 country.

Ariadne VlahakisDepartment of Molecular and Cellular Biology, College of Biological Sciences, University of California, Davis, CA 95616.
Martin GraefDepartment of Molecular and Cellular Biology, College of Biological Sciences, University of California, Davis, CA 95616.
Jodi NunnariDepartment of Molecular and Cellular Biology, College of Biological Sciences, University of California, Davis, CA 95616.
Ted PowersDepartment of Molecular and Cellular Biology, College of Biological Sciences, University of California, Davis, CA 95616 tpowers@ucdavis.edu.
University of California, Davis · US

Funding

UC Davis MCB T32 Administrative Supplement to Recognize Excellence in Diversity, Equity, Inclusion, and Accessibility (DEIA) MentorshipT32GM007377 · NIGMS · UNIVERSITY OF CALIFORNIA DAVIS · PI CHEDIN, FREDERIC LOUIS · 1985 to 2023
$9.9M
The Mechanism of Mitochondrial Fission and Fusion.R01GM062942 · NIGMS · UNIVERSITY OF CALIFORNIA DAVIS · PI NUNNARI, JODI M. · 2001 to 2013
$3.9M
TOR Complex 2 and sphingolipid biosynthesis.R01GM086387 · NIGMS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI POWERS, TED · 2009 to 2012
$1.3M
Mechanisms controlling mitochondrial division and positioningR01GM097432 · NIGMS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI NUNNARI, JODI M. · 2011 to 2014
$1.2M
NIGMS NIH HHS GM086387NIGMS NIH HHS R01 GM062942NIGMS NIH HHS R01GM062942NIGMS NIH HHS R01 GM086387NIGMS NIH HHS R01 GM097432NIGMS NIH HHS R01GM097432NIGMS NIH HHS T32 GM007377
6 · The paper itself

Abstract

The highly conserved Target of Rapamycin (TOR) kinase is a central regulator of cell growth and metabolism in response to nutrient availability. TOR functions in two structurally and functionally distinct complexes, TOR Complex 1 (TORC1) and TOR Complex 2 (TORC2). Through TORC1, TOR negatively regulates autophagy, a conserved process that functions in quality control and cellular homeostasis and, in this capacity, is part of an adaptive nutrient deprivation response. Here we demonstrate that during amino acid starvation TOR also operates independently as a positive regulator of autophagy through the conserved TORC2 and its downstream target protein kinase, Ypk1. Under these conditions, TORC2-Ypk1 signaling negatively regulates the Ca(2+)/calmodulin-dependent phosphatase, calcineurin, to enable the activation of the amino acid-sensing eIF2α kinase, Gcn2, and to promote autophagy. Our work reveals that the TORC2 pathway regulates autophagy in an opposing manner to TORC1 to provide a tunable response to cellular metabolic status.

Indexed as

Amino AcidsAutophagyCalcineurinGlycogen Synthase Kinase 3Mechanistic Target of Rapamycin Complex 2Models, BiologicalMultiprotein ComplexesSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsSignal TransductionTOR Serine-Threonine KinasesAmino AcidsCalcineurinGlycogen Synthase Kinase 3MCK1 protein, S cerevisiaeMechanistic Target of Rapamycin Complex 2Multiprotein ComplexesSaccharomyces cerevisiae ProteinsTOR Serine-Threonine KinasesAtg8Gcn4

Identifiers

PMID25002487
PMCPMC4115538
OpenAlexW2092585317

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.