RapamycinFungusV1, Main, Exploration, bibRecord, 000A57

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

Identifieur interne : 000A57 ( Main/Exploration ); précédent : 000A56; suivant : 000A58

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

Auteurs : Hilla Weidberg [États-Unis] ; Fabien Moretto [Royaume-Uni] ; Gianpiero Spedale [Royaume-Uni] ; Angelika Amon [États-Unis] ; Folkert J. Van Werven [Royaume-Uni]

Source :

PLoS genetics [ 1553-7404 ] ; 2016.

RBID : pubmed:27272508

Descripteurs français

English descriptors

KwdEn :
- Cyclic AMP-Dependent Protein Kinases (antagonists & inhibitors), Cyclic AMP-Dependent Protein Kinases (genetics), Cyclic AMP-Dependent Protein Kinases (metabolism), DNA-Binding Proteins (genetics), Gametogenesis (genetics), Meiosis (genetics), Nuclear Proteins (antagonists & inhibitors), Nuclear Proteins (metabolism), Promoter Regions, Genetic (MeSH), Protein-Serine-Threonine Kinases (metabolism), Repressor Proteins (metabolism), Saccharomyces cerevisiae (genetics), Saccharomyces cerevisiae Proteins (antagonists & inhibitors), Saccharomyces cerevisiae Proteins (genetics), Saccharomyces cerevisiae Proteins (metabolism), Signal Transduction (genetics), Spores, Fungal (metabolism), Transcription Factors (antagonists & inhibitors), Transcription Factors (genetics), Transcription Factors (metabolism).
MESH :
- chemical , antagonists & inhibitors : Cyclic AMP-Dependent Protein Kinases, Nuclear Proteins, Saccharomyces cerevisiae Proteins, Transcription Factors.
- chemical , genetics : Cyclic AMP-Dependent Protein Kinases, DNA-Binding Proteins, Saccharomyces cerevisiae Proteins, Transcription Factors.
- chemical , metabolism : Cyclic AMP-Dependent Protein Kinases, Nuclear Proteins, Protein-Serine-Threonine Kinases, Repressor Proteins, Saccharomyces cerevisiae Proteins, Transcription Factors.
- genetics : Gametogenesis, Meiosis, Saccharomyces cerevisiae, Signal Transduction.
- metabolism : Spores, Fungal.
- Promoter Regions, Genetic.

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.

DOI: 10.1371/journal.pgen.1006075
PubMed: 27272508
PubMed Central: PMC4894626

Affiliations:

Links toward previous steps (curation, corpus...)

to stream Main, to step Corpus: 000A34
to stream Main, to step Curation: 000A34

Le document en format XML

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<term>DNA-Binding Proteins (genetics)</term>
<term>Gametogenesis (genetics)</term>
<term>Meiosis (genetics)</term>
<term>Nuclear Proteins (antagonists & inhibitors)</term>
<term>Nuclear Proteins (metabolism)</term>
<term>Promoter Regions, Genetic (MeSH)</term>
<term>Protein-Serine-Threonine Kinases (metabolism)</term>
<term>Repressor Proteins (metabolism)</term>
<term>Saccharomyces cerevisiae (genetics)</term>
<term>Saccharomyces cerevisiae Proteins (antagonists & inhibitors)</term>
<term>Saccharomyces cerevisiae Proteins (genetics)</term>
<term>Saccharomyces cerevisiae Proteins (metabolism)</term>
<term>Signal Transduction (genetics)</term>
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<term>Facteurs de transcription (antagonistes et inhibiteurs)</term>
<term>Facteurs de transcription (génétique)</term>
<term>Facteurs de transcription (métabolisme)</term>
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<term>Protéines nucléaires (métabolisme)</term>
<term>Régions promotrices (génétique) (MeSH)</term>
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<front><div type="abstract" xml:lang="en">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.</div>
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<Abstract><AbstractText>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.</AbstractText>
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Nutrient Control of Yeast Gametogenesis Is Mediated by TORC1, PKA and Energy Availability.

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

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