| Literature DB >> 32898476 |
Shu Yang1, Yingbiao Zhang1, Chun-Yuan Ting1, Lucia Bettedi1, Kuikwon Kim1, Elena Ghaniam1, Mary A Lilly2.
Abstract
The dysregulation of the metabolic regulator TOR complex I (TORC1) contributes to a wide array of human pathologies. Tuberous sclerosis complex (TSC) is a potent inhibitor of TORC1. Here, we demonstrate that the Rag GTPase acts in both the amino-acid-sensing and growth factor signaling pathways to control TORC1 activity through the regulation of TSC dynamics in HeLa cells and Drosophila. We find that TSC lysosomal-cytosolic exchange increases in response to both amino acid and growth factor restriction. Moreover, the rate of exchange mirrors TSC function, with depletions of the Rag GTPase blocking TSC lysosomal mobility and rescuing TORC1 activity. Finally, we show that the GATOR2 complex controls the phosphorylation of TSC2, which is essential for TSC exchange. Our data support the model that the amino acid and growth factor signaling pathways converge on the Rag GTPase to inhibit TORC1 activity through the regulation of TSC dynamics. Published by Elsevier Inc.Entities:
Keywords: AKT1; Drosophila; GATOR2; HeLa cell; Rag GTPase; TORC1; TSC; amino acid signaling; growth factor signaling; lysosome
Year: 2020 PMID: 32898476 PMCID: PMC7657977 DOI: 10.1016/j.devcel.2020.08.006
Source DB: PubMed Journal: Dev Cell ISSN: 1534-5807 Impact factor: 12.270