Evidence map›Paper›PMID 25428989›Full record

ArticleMolecular biology of the cell2015

PAS kinase is activated by direct SNF1-dependent phosphorylation and mediates inhibition of TORC1 through the phosphorylation and activation of Pbp1.

Desiree DeMille, Bryan D Badal, J Brady Evans, Andrew D Mathis, Joseph F Anderson, Julianne H Grose

Abstract read
In one paragraph

Article in Molecular biology of the cell, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

28 citing papers in PubMed, 57 citations in OpenAlex.

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  10. Mid-Gestation lethality ofInternational journal of molecular sciences · 2020
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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

6 authors at 1 institution in 1 country.

Desiree DeMilleDepartment of Microbiology and Molecular Biology, Brigham Young University, Provo, UT 84602.
Bryan D BadalDepartment of Microbiology and Molecular Biology, Brigham Young University, Provo, UT 84602.
J Brady EvansDepartment of Microbiology and Molecular Biology, Brigham Young University, Provo, UT 84602.
Andrew D MathisDepartment of Chemistry, Brigham Young University, Provo, UT 84602.
Joseph F AndersonDepartment of Microbiology and Molecular Biology, Brigham Young University, Provo, UT 84602.
Julianne H GroseDepartment of Microbiology and Molecular Biology, Brigham Young University, Provo, UT 84602 julianne_grose@byu.edu.
Brigham Young University · US

Funding

Regulation and Function of PAS Kinase - PASsing glucose to control respiration, lipogenesis and cell cycleR15GM100376 · NIGMS · BRIGHAM YOUNG UNIVERSITY · PI GROSE, JULIANNE H. · 2012 to 2022
$1.3M
NIGMS NIH HHS R15 GM100376NIGMS NIH HHS R15 GM100376-01
6 · The paper itself

Abstract

We describe the interplay between three sensory protein kinases in yeast: AMP-regulated kinase (AMPK, or SNF1 in yeast), PAS kinase 1 (Psk1 in yeast), and the target of rapamycin complex 1 (TORC1). This signaling cascade occurs through the SNF1-dependent phosphorylation and activation of Psk1, which phosphorylates and activates poly(A)- binding protein binding protein 1 (Pbp1), which then inhibits TORC1 through sequestration at stress granules. The SNF1-dependent phosphorylation of Psk1 appears to be direct, in that Snf1 is necessary and sufficient for Psk1 activation by alternate carbon sources, is required for altered Psk1 protein mobility, is able to phosphorylate Psk1 in vitro, and binds Psk1 via its substrate-targeting subunit Gal83. Evidence for the direct phosphorylation and activation of Pbp1 by Psk1 is also provided by in vitro and in vivo kinase assays, including the reduction of Pbp1 localization at distinct cytoplasmic foci and subsequent rescue of TORC1 inhibition in PAS kinase-deficient yeast. In support of this signaling cascade, Snf1-deficient cells display increased TORC1 activity, whereas cells containing hyperactive Snf1 display a PAS kinase-dependent decrease in TORC1 activity. This interplay between yeast SNF1, Psk1, and TORC1 allows for proper glucose allocation during nutrient depletion, reducing cell growth and proliferation when energy is low.

Indexed as

Carrier ProteinsCell ProliferationDown-RegulationEnzyme ActivationGlucoseMechanistic Target of Rapamycin Complex 1Multiprotein ComplexesPhosphorylationProtein KinasesProtein Serine-Threonine KinasesSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsSignal TransductionTOR Serine-Threonine KinasesCarrier ProteinsGlucoseMechanistic Target of Rapamycin Complex 1Multiprotein ComplexesPBP1 protein, S cerevisiaeProtein KinasesProtein Serine-Threonine KinasesPSK1 protein, S cerevisiaeSaccharomyces cerevisiae ProteinsSNF1-related protein kinasesTOR Serine-Threonine Kinases

Identifiers

PMID25428989
PMCPMC4310746
OpenAlexW2149202384

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.