Evidence map›Paper›PMID 28007891›Full record

ArticleGenetics2017

General Amino Acid Control and 14-3-3 Proteins Bmh1/2 Are Required for Nitrogen Catabolite Repression-Sensitive Regulation of Gln3 and Gat1 Localization.

Jennifer J Tate, David Buford, Rajendra Rai, Terrance G Cooper

Open access · bronzeAbstract read
In one paragraph

Article in Genetics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
3.1field-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

21 citing papers in PubMed, 32 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. A Gene fromJournal of fungi (Basel, Switzerland) · 2023
    Article
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  6. Article
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  12. Review
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  15. Article
  16. Complete genome sequence and analysis of the industrial Saccharomyces cerevisiae strain N85 used in Chinese rice wine production.DNA research : an international journal for rapid publication of reports on genes and genomes · 2018
    Article
  17. Review
  18. Article
  19. QuantitativeMicrobial biotechnology · 2017
    Article
  20. Review
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.

Jennifer J TateDepartment of Microbiology, Immunology, and Biochemistry, University of Tennessee Health Science Center, Memphis, Tennessee 38163.
David BufordDepartment of Microbiology, Immunology, and Biochemistry, University of Tennessee Health Science Center, Memphis, Tennessee 38163.
Rajendra RaiDepartment of Microbiology, Immunology, and Biochemistry, University of Tennessee Health Science Center, Memphis, Tennessee 38163.
Terrance G CooperDepartment of Microbiology, Immunology, and Biochemistry, University of Tennessee Health Science Center, Memphis, Tennessee 38163 tcooper@uthsc.edu.
University of Tennessee Health Science Center · US

Funding

SYNTHESIS AND ASSEMBLY OF EUKARYOTIC MEMBRANESR01GM035642 · NIGMS · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI COOPER, TERRANCE G. · 1985 to 2015
$4.3M
NIGMS NIH HHS R01 GM035642
6 · The paper itself

Abstract

Nitrogen catabolite repression (NCR), the ability of Saccharomyces cerevisiae to use good nitrogen sources in preference to poor ones, derives from nitrogen-responsive regulation of the GATA family transcription activators Gln3 and Gat1 In nitrogen-replete conditions, the GATA factors are cytoplasmic and NCR-sensitive transcription minimal. When only poor nitrogen sources are available, Gln3 is nuclear, dramatically increasing GATA factor-mediated transcription. This regulation was originally attributed to mechanistic Tor protein kinase complex 1 (mTorC1)-mediated control of Gln3 However, we recently showed that two regulatory systems act cumulatively to maintain cytoplasmic Gln3 sequestration, only one of which is mTorC1. Present experiments demonstrate that the other previously elusive component is uncharged transfer RNA-activated, Gcn2 protein kinase-mediated general amino acid control (GAAC). Gcn2 and Gcn4 are required for NCR-sensitive nuclear Gln3-Myc

Indexed as

Protein Processing, Post-Translational14-3-3 ProteinsActive Transport, Cell NucleusAmino AcidsBasic-Leucine Zipper Transcription FactorsCatabolite RepressionCell NucleusEpistasis, GeneticGATA Transcription FactorsGlutathione PeroxidaseMechanistic Target of Rapamycin Complex 1Multiprotein ComplexesNitrogenPhosphorylationPrionsProtein Serine-Threonine Kinases14-3-3 ProteinsAmino AcidsBasic-Leucine Zipper Transcription FactorsGAT1 protein, S cerevisiaeGATA Transcription FactorsGCN2 protein, S cerevisiaeGCN4 protein, S cerevisiaeGLN3 protein, S cerevisiaeGlutathione PeroxidaseMechanistic Target of Rapamycin Complex 1Multiprotein ComplexesNitrogenPrionsProtein Serine-Threonine KinasesSaccharomyces cerevisiae ProteinsTOR Serine-Threonine KinasesTranscription FactorsURE2 protein, S cerevisiaeBmh1/2Gat1Gcn2Gln3nitrogen catabolite repression

Identifiers

PMID28007891
PMCPMC5289842
OpenAlexW2562339613

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.