Literature DB >> 32898476

The Rag GTPase Regulates the Dynamic Behavior of TSC Downstream of Both Amino Acid and Growth Factor Restriction.

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


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