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

Autor: Hilla Weidberg, Angelika Amon, Fabien Moretto, Folkert J. van Werven, Gianpiero Spedale
Přispěvatelé: Koch Institute for Integrative Cancer Research at MIT, Weidberg, Hilla, Amon, Angelika B.
Jazyk: angličtina
Rok vydání: 2015
Předmět:
0301 basic medicine
Cell signaling
Cancer Research
Physiology
Signal transduction
Biochemistry
Gametogenesis
Fungal Reproduction
Reproductive Physiology
Transcription (biology)
Medicine and Health Sciences
Cell Cycle and Cell Division
Promoter Regions
Genetic

Fungal Sporulation
Genetics (clinical)
biology
Chromosome Biology
Organic Compounds
Messenger RNA
Monosaccharides
Nuclear Proteins
Signaling cascades
Spores
Fungal

PKA signaling cascade
DNA-Binding Proteins
Nucleic acids
Meiosis
Chemistry
Cell Processes
Physical Sciences
Energy source
Research Article
Cell biology
Saccharomyces cerevisiae Proteins
lcsh:QH426-470
Saccharomyces cerevisiae
Carbohydrates
Repressor
Mycology
Protein Serine-Threonine Kinases
Cell fate determination
Glucose Signaling
03 medical and health sciences
Genetics
Protein kinase A
Molecular Biology
Transcription factor
Ecology
Evolution
Behavior and Systematics

Biology and life sciences
Organic Chemistry
Chemical Compounds
biology.organism_classification
Cyclic AMP-Dependent Protein Kinases
Repressor Proteins
lcsh:Genetics
Glucose
030104 developmental biology
RNA
Transcription Factors
Zdroj: PLOS
PLoS Genetics, Vol 12, Iss 6, p e1006075 (2016)
PLoS Genetics
Popis: 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.
Jane Coffin Childs Memorial Fund for Medical Research
European Molecular Biology Organization (EMBO Long-term Fellowship)
Weizmann Institute of Science (Israel National Postdoctoral Program for Advancing Women in Science)
National Institutes of Health (U.S.) (NIH grant GM62207)
Francis Crick Institute
Databáze: OpenAIRE