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Measuring Replicative Life Span in the Budding Yeast
Published on: June 25, 2009
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The TORC1-Nem1/Spo7-Pah1/lipin axis regulates microautophagy induction in budding yeast
Muhammad Arifur Rahman1, Mashu Terasawa2, Md Golam Mostofa1
1Graduate School of Science and Technology, Shizuoka University, Ohya 836, Suruga-ku, Shizuoka, 422-8021, Japan.
Biochemical and Biophysical Research Communications
|September 12, 2018
Summary
Nutrient starvation inactivates the target of rapamycin complex 1 (TORC1) kinase, inducing both macroautophagy and microautophagy. This process requires the Nem1/Spo7-Pah1 pathway and Vps27, revealing a master regulator for yeast autophagy.
Area of Science:
- Cellular biology
- Molecular biology
- Yeast genetics
Background:
- Nutrient starvation and target of rapamycin complex 1 (TORC1) inhibition are known inducers of macroautophagy.
- Macroautophagy is a lipid-consuming cellular process.
- The regulation of microautophagy by TORC1 has been debated.
Purpose of the Study:
- To investigate the role of TORC1 signaling in the regulation of microautophagy.
- To identify key proteins and pathways involved in TORC1-mediated microautophagy induction.
Main Methods:
- Utilized budding yeast Saccharomyces cerevisiae as a model organism.
- Investigated the requirement of specific genes (Vps27, Atg1, Atg7, Atg8) in microautophagy induction.
- Examined the role of the Nem1/Spo7-Pah1 axis in TORC1 inactivation-induced microautophagy.
Main Results:
- TORC1 inactivation was found to induce microautophagy in budding yeast.
- Vps27 was identified as essential for TORC1 inactivation-induced microautophagy, while Atg1, Atg7, and Atg8 were not.
- The Nem1/Spo7-Pah1 protein phosphatase pathway was critical for microautophagy induction.
Conclusions:
- The TORC1 signaling pathway, through the Nem1/Spo7-Pah1 axis, acts as a master regulator of both macroautophagy and microautophagy in budding yeast.
- This study elucidates a conserved regulatory mechanism for different types of autophagy in response to nutrient availability.
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