TORC1 Regulates Developmental Responses to Nitrogen Stress via Regulation of the GATA Transcription Factor Gaf1
Dana Laor1, Adiel Cohen2, Martin Kupiec1
1Department of Molecular Microbiology and Biotechnology, Tel Aviv University, Tel Aviv, Israel.
Unlabelled:
The TOR (target of rapamycin [sirolimus]) is a universally conserved kinase that couples nutrient availability to cell growth. TOR complex 1 (TORC1) in Schizosaccharomyces pombe positively regulates growth in response to nitrogen availability while suppressing cellular responses to nitrogen stress. Here we report the identification of the GATA transcription factor Gaf1 as a positive regulator of the nitrogen stress-induced gene isp7(+), via three canonical GATA motifs. We show that under nitrogen-rich conditions, TORC1 positively regulates the phosphorylation and cytoplasmic retention of Gaf1 via the PP2A-like phosphatase Ppe1. Under nitrogen stress conditions when TORC1 is inactivated, Gaf1 becomes dephosphorylated and enters the nucleus. Gaf1 was recently shown to negatively regulate the transcription induction of ste11(+), a major regulator of sexual development. Our findings support a model of a two-faceted role of Gaf1 during nitrogen stress. Gaf1 positively regulates genes that are induced early in the response to nitrogen stress, while inhibiting later responses, such as sexual development. Taking these results together, we identify Gaf1 as a novel target for TORC1 signaling and a step-like mechanism to modulate the nitrogen stress response.
Importance:
TOR complex 1 (TORC1) is an evolutionary conserved protein complex that positively regulates growth and proliferation, while inhibiting starvation responses. In fission yeast, the activity of TORC1 is downregulated in response to nitrogen starvation, and cells reprogram their transcriptional profile and prepare for sexual development. We identify Gaf1, a GATA-like transcription factor that regulates transcription and sexual development in response to starvation, as a downstream target for TORC1 signaling. Under nitrogen-rich conditions, TORC1 positively regulates the phosphorylation and cytoplasmic retention of Gaf1 via the PP2A-like phosphatase Ppe1. Under nitrogen stress conditions when TORC1 is inactivated, Gaf1 becomes dephosphorylated and enters the nucleus. Budding yeast TORC1 regulates GATA transcription factors via the phosphatase Sit4, a structural homologue of Ppe1. Thus, the TORC1-GATA transcription module appears to be conserved in evolution and may also be found in higher eukaryotes.
Insights
The target of rapamycin complex 1 (TORC1) pathway regulates the GATA transcription factor Gaf1. TORC1 controls Gaf1
Area of Science:
- Cellular Biology
- Molecular Biology
- Genetics
Background:
- The target of rapamycin (TOR) pathway is a central regulator of cell growth, nutrient sensing, and stress responses.
- TOR complex 1 (TORC1) in Schizosaccharomyces pombe (fission yeast) promotes growth under nutrient-rich conditions and suppresses stress responses.
- Nitrogen starvation inactivates TORC1, leading to transcriptional reprogramming and preparation for sexual development.
Purpose of the Study:
- To identify downstream targets of TORC1 signaling involved in nitrogen stress response.
- To elucidate the role of the GATA transcription factor Gaf1 in mediating TORC1's effects on nitrogen stress and sexual development.
- To investigate the mechanism by which TORC1 regulates Gaf1 activity and localization.
Main Methods:
- Identification of Gaf1 as a regulator of the nitrogen stress-induced gene isp7(+).
- Analysis of Gaf1 phosphorylation and nuclear localization under varying nitrogen conditions.
- Investigation of TORC1-mediated regulation of Gaf1 via the phosphatase Ppe1.
Main Results:
- Gaf1 directly regulates the nitrogen stress-induced gene isp7(+) through GATA motifs.
- TORC1 positively regulates Gaf1 phosphorylation and cytoplasmic retention via Ppe1 under nutrient-rich conditions.
- Upon nitrogen stress and TORC1 inactivation, Gaf1 is dephosphorylated, enters the nucleus, and modulates gene expression, including inhibiting sexual development regulators like ste11(+).
Conclusions:
- Gaf1 acts as a novel downstream target of TORC1 signaling, integrating nutrient availability with cellular stress responses.
- Gaf1 exhibits a dual role in nitrogen stress: promoting early stress gene induction while suppressing later sexual development.
- The TORC1-Gaf1 regulatory module represents a conserved mechanism for modulating stress responses, potentially conserved in higher eukaryotes.
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