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Published on: March 3, 2015
Pib2 is a cysteine sensor involved in TORC1 activation in Saccharomyces cerevisiae
Qingzhong Zeng1, Yasuhiro Araki2, Takeshi Noda3
1Graduate School of Frontier Biosciences, Osaka University, Osaka 565-0871, Japan.
Abstract:
Target of rapamycin complex 1 (TORC1) is a master regulator that monitors the availability of various amino acids to promote cell growth in Saccharomyces cerevisiae. It is activated via two distinct upstream pathways: the Gtr pathway, which corresponds to mammalian Rag, and the Pib2 pathway. This study shows that Ser3 was phosphorylated exclusively in a Pib2-dependent manner. Using Ser3 as an indicator of TORC1 activity, together with the established TORC1 substrate Sch9, we investigated which pathways were employed by individual amino acids. Different amino acids exhibited different dependencies on the Gtr and Pib2 pathways. Cysteine was most dependent on the Pib2 pathway and increased the interaction between TORC1 and Pib2 in vivo and in vitro. Moreover, cysteine directly bound to Pib2 via W632 and F635, two critical residues in the T(ail) motif that are necessary to activate TORC1. These results indicate that Pib2 functions as a sensor for cysteine in TORC1 regulation.
Insights
Target of rapamycin complex 1 (TORC1) regulates cell growth by sensing amino acids. This study reveals cysteine directly activates TORC1 via the Pib2 pathway, identifying Pib2 as a cysteine sensor.
Area of Science:
- Cellular biology
- Molecular mechanisms of nutrient sensing
- Yeast as a model organism
Background:
- Target of rapamycin complex 1 (TORC1) is crucial for cell growth, integrating nutrient availability signals.
- TORC1 activation in Saccharomyces cerevisiae involves the Gtr and Pib2 pathways.
- Amino acid availability dictates TORC1 pathway utilization.
Purpose of the Study:
- To elucidate the specific roles of the Gtr and Pib2 pathways in TORC1 activation by individual amino acids.
- To investigate the mechanism by which cysteine influences TORC1 signaling.
- To identify the direct interaction between cysteine and its sensor protein.
Main Methods:
- Phosphorylation analysis of TORC1 substrate Ser3 to indicate pathway activity.
- Assessing TORC1 activity using the substrate Sch9.
- In vivo and in vitro interaction studies between TORC1, Pib2, and cysteine.
- Site-directed mutagenesis to identify critical residues in Pib2.
Main Results:
- Different amino acids display distinct dependencies on the Gtr and Pib2 pathways for TORC1 activation.
- Cysteine exhibits a strong dependence on the Pib2 pathway.
- Cysteine directly binds to Pib2 at residues W632 and F635 within the T(ail) motif, enhancing TORC1-Pib2 interaction.
- Pib2 acts as a direct sensor for cysteine.
Conclusions:
- Pib2 is identified as a specific cysteine sensor for TORC1 regulation.
- Cysteine directly activates TORC1 through Pib2-mediated signaling.
- This study reveals a novel mechanism of amino acid sensing in nutrient-regulated growth.
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