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Autophagy ; 13(3): 464-472, 2017 Mar 04.
Article in English | MEDLINE | ID: mdl-28055300

ABSTRACT

The master regulator of lysosome biogenesis, TFEB, is regulated by MTORC1 through phosphorylation at S211, and a S211A mutation increases nuclear localization. However, TFEBS211A localizes diffusely in both cytoplasm and nucleus and, as we show, retains regulation by MTORC1. Here, we report that endogenous TFEB is phosphorylated at S122 in an MTORC1-dependent manner, that S122 is phosphorylated in vitro by recombinant MTOR, and that S122 is important for TFEB regulation by MTORC1. Specifically, nuclear localization following MTORC1 inhibition is blocked by a S122D mutation (despite S211 dephosphorylation). Furthermore, such a mutation inhibits lysosomal biogenesis induced by Torin1. These data reveal a novel mechanism of TFEB regulation by MTORC1 essential for lysosomal biogenesis.


Subject(s)
Basic Helix-Loop-Helix Leucine Zipper Transcription Factors/metabolism , Mechanistic Target of Rapamycin Complex 1/metabolism , Animals , Cell Nucleus/drug effects , Cell Nucleus/metabolism , HeLa Cells , Humans , Lysosomes/drug effects , Lysosomes/metabolism , Mice , Models, Biological , Naphthyridines/pharmacology , Organelle Biogenesis , Phosphorylation/drug effects , Phosphoserine/metabolism , Protein Transport/drug effects
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