Affiliation
Department of Molecular and Cellular Biology, University of ArizonaIssue Date
2022
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eLife Sciences Publications Ltd.Citation
Wallace, R. L., Lu, E., Luo, X., & Capaldi, A. P. (2022). Ait1 regulates TORC1 signaling and localization in budding yeast. ELife, 11.Journal
eLifeRights
Copyright © Wallace, Lu et al. This article is distributed under the terms of the Creative Commons Attribution License.Collection Information
This item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.Abstract
The target of rapamycin complex I (TORC1) regulates cell growth and metabolism in eukaryotes. Previous studies have shown that nitrogen and amino acid signals activate TORC1 via the highly conserved small GTPases, Gtr1/2 (RagA/C in humans), and the GTPase activating complex SEAC/GATOR. However, it remains unclear if, and how, other proteins/pathways regulate TORC1 in simple eukaryotes like yeast. Here, we report that the previously unstudied GPCR-like protein, Ait1, binds to TORC1-Gtr1/2 in Saccharomyces cerevisiae and holds TORC1 around the vacuole during log-phase growth. Then, during amino acid starvation, Ait1 inhibits TORC1 via Gtr1/2 using a loop that resembles the RagA/C-binding domain in the human protein SLC38A9. Importantly, Ait1 is only found in the Saccharomycetaceae/codaceae, two closely related families of yeast that have lost the ancient TORC1 regulators Rheb and TSC1/2. Thus, the TORC1 circuit found in the Saccharomycetaceae/codaceae, and likely other simple eukaryotes, has undergone significant rewiring during evolution. © 2022, Wallace, Lu et al.Note
Open access journalISSN
2050-084XPubMed ID
36047762Version
Final published versionae974a485f413a2113503eed53cd6c53
10.7554/eLife.68773
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Except where otherwise noted, this item's license is described as Copyright © Wallace, Lu et al. This article is distributed under the terms of the Creative Commons Attribution License.
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