Evidence map›Paper›PMID 20233714›Full record

ArticleThe Journal of biological chemistry2010

Integration of general amino acid control and target of rapamycin (TOR) regulatory pathways in nitrogen assimilation in yeast.

Kirk A Staschke, Souvik Dey, John M Zaborske, Lakshmi Reddy Palam, Jeanette N McClintick, Tao Pan, Howard J Edenberg, Ronald C Wek

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 69 papers.

0numbers the graph read from it
0cells of the map it votes in
69citing papers in PubMed
5.4field-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

69 citing papers in PubMed, 129 citations in OpenAlex.

  1. Article
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  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Multiple Roles of the Stress Sensor GCN2 in Immune Cells.International journal of molecular sciences · 2023
    Review
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  11. Article
  12. Effect of Shock Waves on the Growth ofJournal of fungi (Basel, Switzerland) · 2022
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Review

9 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

8 authors at 3 institutions in 1 country.

Kirk A StaschkeDepartment of Biochemistry and Molecular Biology, Indiana University School of Medicine, Indianapolis, Indiana 46202, USA.
Souvik Dey
John M Zaborske
Lakshmi Reddy Palam
Jeanette N McClintick
Tao Pan
Howard J Edenberg
Ronald C Wek
Indiana University School of MedicineUniversity of Chicago · USIndiana University – Purdue University Indianapolis · US

Funding

Metabolic stress responses andeIF2 kinase GCN2R01GM049164 · NIGMS · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI WEK, RONALD C · 1998 to 2019
$6.3M
NIGMS NIH HHS R01 GM049164NIGMS NIH HHS R01GM49164
6 · The paper itself

Abstract

Two important nutrient-sensing and regulatory pathways, the general amino acid control (GAAC) and the target of rapamycin (TOR), participate in the control of yeast growth and metabolism during changes in nutrient availability. Amino acid starvation activates the GAAC through Gcn2p phosphorylation of translation factor eIF2 and preferential translation of GCN4, a transcription activator. TOR senses nitrogen availability and regulates transcription factors such as Gln3p. We used microarray analyses to address the integration of the GAAC and TOR pathways in directing the yeast transcriptome during amino acid starvation and rapamycin treatment. We found that GAAC is a major effector of the TOR pathway, with Gcn4p and Gln3p each inducing a similar number of genes during rapamycin treatment. Although Gcn4p activates a common core of 57 genes, the GAAC directs significant variations in the transcriptome during different stresses. In addition to inducing amino acid biosynthetic genes, Gcn4p in conjunction with Gln3p activates genes required for the assimilation of secondary nitrogen sources such as gamma-aminobutyric acid (GABA). Gcn2p activation upon shifting to secondary nitrogen sources is suggested to occur by means of a dual mechanism. First, Gcn2p is induced by the release of TOR repression through a mechanism involving Sit4p protein phosphatase. Second, this eIF2 kinase is activated by select uncharged tRNAs, which were shown to accumulate during the shift to the GABA medium. This study highlights the mechanisms by which the GAAC and TOR pathways are integrated to recognize changing nitrogen availability and direct the transcriptome for optimal growth adaptation.

Indexed as

Gene Expression RegulationAmino Acidsgamma-Aminobutyric AcidGene Expression ProfilingIntracellular Signaling Peptides and ProteinsModels, BiologicalNitrogenPhosphorylationProtein BiosynthesisProtein Phosphatase 2Protein Serine-Threonine KinasesRNA, TransferSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsSpecies SpecificityTOR Serine-Threonine KinasesAmino Acidsgamma-Aminobutyric AcidGCN2 protein, S cerevisiaeIntracellular Signaling Peptides and ProteinsNitrogenProtein Phosphatase 2Protein Serine-Threonine KinasesRNA, TransferSaccharomyces cerevisiae ProteinsSIT4 protein, S cerevisiaeTOR Serine-Threonine Kinases

Identifiers

PMID20233714
PMCPMC2878067
OpenAlexW2001007338

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.