Evidence map›Paper›PMID 18443284›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2008

Nuclear translocation of Gln3 in response to nutrient signals requires Golgi-to-endosome trafficking in Saccharomyces cerevisiae.

Rekha Puria, Sara A Zurita-Martinez, Maria E Cardenas

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

33 citing papers in PubMed, 50 citations in OpenAlex.

  1. Article
  2. Article
  3. Nutrient and Stress Sensing in Pathogenic Yeasts.Frontiers in microbiology · 2019
    Review
  4. Review
  5. Phosphate is the third nutrient monitored by TOR inProceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
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  12. Article
  13. Article
  14. Review
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  16. Article
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  18. Article
  19. Amino acids and mTORC1: from lysosomes to disease.Trends in molecular medicine · 2012
    Review
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors at 2 institutions in 1 country.

Rekha PuriaDepartment of Molecular Genetics and Microbiology, Duke University Medical Center, Durham, NC 27710, USA.
Sara A Zurita-Martinez
Maria E Cardenas
Duke Medical Center · USDuke University · US

Funding

Signaling mechanisms by the rapamycin target: Tor kinaseR01CA114107 · NCI · DUKE UNIVERSITY · PI CARDENAS-CORONA, MARIA E · 2005 to 2009
$1.3M
NCI NIH HHS CA114107NCI NIH HHS R01 CA114107
6 · The paper itself

Abstract

The yeast Saccharomyces cerevisiae has developed specialized mechanisms that enable growth on suboptimal nitrogen sources. Exposure of yeast cells to poor nitrogen sources or treatment with the Tor kinase inhibitor rapamycin elicits activation of Gln3 and transcription of nitrogen catabolite-repressed (NCR) genes whose products function in scavenging and metabolizing nitrogen. Here, we show that mutations in class C and D Vps components, which mediate Golgi-to-endosome vesicle transport, impair nuclear translocation of Gln3, NCR gene activation, and growth in poor nitrogen sources. In nutrient-replete conditions, a significant fraction of Gln3 is peripherally associated with light membranes and partially colocalizes with Vps10-containing foci. These results reveal a role for Golgi-to-endosome vesicular trafficking in TORC1-controlled nuclear translocation of Gln3 and support a model in which Tor-mediated signaling in response to nutrient cues occurs in these compartments. These findings have important implications for nutrient sensing and growth control via mTor pathways in metazoans.

Indexed as

Gene Expression Regulation, FungalActive Transport, Cell NucleusCell MembraneCell NucleusEndosomesGenes, FungalGolgi ApparatusModels, BiologicalMutationNitrogenRepressor ProteinsSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsSubcellular FractionsTranscriptional ActivationTranscription FactorsGLN3 protein, S cerevisiaeNitrogenPEP1 protein, S cerevisiaeRepressor ProteinsSaccharomyces cerevisiae ProteinsTranscription FactorsVesicular Transport Proteins

Identifiers

PMID18443284
PMCPMC2438226
OpenAlexW2042543993

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.