Evidence map›Paper›PMID 27272508›Full record

ArticlePLoS genetics2016

Nutrient Control of Yeast Gametogenesis Is Mediated by TORC1, PKA and Energy Availability.

Hilla Weidberg, Fabien Moretto, Gianpiero Spedale, Angelika Amon, Folkert J van Werven

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2016. 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 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

28 citing papers in PubMed, 42 citations in OpenAlex.

  1. Article
  2. Regulation of Translation by PKA Signaling Pathway.International journal of molecular sciences · 2026
    Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
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  9. Article
  10. Article
  11. eLife · 2022
    Article
  12. Article
  13. Article
  14. Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. mNature communications · 2019
    Article
  20. Article
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

5 authors at 3 institutions in 2 countries.

Hilla WeidbergDavid H. Koch Institute for Integrative Cancer Research and Howard Hughes Medical Institute, Massachusetts Institute of Technology, Cambridge, Massachusetts, United States of America.
Fabien MorettoCell Fate and Gene Regulation Laboratory, The Francis Crick Institute, London, United Kingdom.
Gianpiero SpedaleCell Fate and Gene Regulation Laboratory, The Francis Crick Institute, London, United Kingdom.
Angelika AmonDavid H. Koch Institute for Integrative Cancer Research and Howard Hughes Medical Institute, Massachusetts Institute of Technology, Cambridge, Massachusetts, United States of America.
Folkert J van WervenCell Fate and Gene Regulation Laboratory, The Francis Crick Institute, London, United Kingdom.
The Francis Crick Institute · GBHoward Hughes Medical Institute · USMassachusetts Institute of Technology · US

Funding

REGULATION OF THE MEIOTIC CELL CYCLER01GM062207 · NIGMS · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI AMON, ANGELIKA B · 2001 to 2016
$3.8M
Causes and consequences of aneuploidyR35GM118066 · NIGMS · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI AMON, ANGELIKA B · 2016 to 2020
$1.9M
Cancer Research UK 17576NIGMS NIH HHS R01 GM062207NIGMS NIH HHS R35 GM118066Wellcome Trust
6 · The paper itself

Abstract

Cell fate choices are tightly controlled by the interplay between intrinsic and extrinsic signals, and gene regulatory networks. In Saccharomyces cerevisiae, the decision to enter into gametogenesis or sporulation is dictated by mating type and nutrient availability. These signals regulate the expression of the master regulator of gametogenesis, IME1. Here we describe how nutrients control IME1 expression. We find that protein kinase A (PKA) and target of rapamycin complex I (TORC1) signalling mediate nutrient regulation of IME1 expression. Inhibiting both pathways is sufficient to induce IME1 expression and complete sporulation in nutrient-rich conditions. Our ability to induce sporulation under nutrient rich conditions allowed us to show that respiration and fermentation are interchangeable energy sources for IME1 transcription. Furthermore, we find that TORC1 can both promote and inhibit gametogenesis. Down-regulation of TORC1 is required to activate IME1. However, complete inactivation of TORC1 inhibits IME1 induction, indicating that an intermediate level of TORC1 signalling is required for entry into sporulation. Finally, we show that the transcriptional repressor Tup1 binds and represses the IME1 promoter when nutrients are ample, but is released from the IME1 promoter when both PKA and TORC1 are inhibited. Collectively our data demonstrate that nutrient control of entry into sporulation is mediated by a combination of energy availability, TORC1 and PKA activities that converge on the IME1 promoter.

Indexed as

Cyclic AMP-Dependent Protein KinasesDNA-Binding ProteinsGametogenesisMeiosisNuclear ProteinsPromoter Regions, GeneticProtein Serine-Threonine KinasesRepressor ProteinsSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsSignal TransductionSpores, FungalTranscription FactorsCyclic AMP-Dependent Protein KinasesDNA-Binding ProteinsIME1 protein, S cerevisiaeNuclear ProteinsProtein Serine-Threonine KinasesRepressor ProteinsSaccharomyces cerevisiae ProteinsSCH9 protein, S cerevisiaeTORC1 protein complex, S cerevisiaeTranscription FactorsTUP1 protein, S cerevisiae

Identifiers

PMID27272508
PMCPMC4894626
OpenAlexW2418873112

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.