p62 is a key regulator of nutrient sensing in the mTORC1 pathway.

Titlep62 is a key regulator of nutrient sensing in the mTORC1 pathway.
Publication TypeJournal Article
Year of Publication2011
AuthorsDuran A, Amanchy R, Linares JF, Joshi J, Abu-Baker S, Porollo A, Hansen M, Moscat J, Diaz-Meco MT
JournalMol Cell
Volume44
Issue1
Pagination134-46
Date Published2011 Oct 07
ISSN1097-4164
KeywordsAdaptor Proteins, Signal Transducing, Animals, Autophagy, Carrier Proteins, Dimerization, GTP Phosphohydrolases, Heat-Shock Proteins, HEK293 Cells, Humans, Intracellular Signaling Peptides and Proteins, Lysosomes, Mechanistic Target of Rapamycin Complex 1, Mice, Multiprotein Complexes, NIH 3T3 Cells, Plasmids, Protein Kinase C, Proteins, Regulatory-Associated Protein of mTOR, Sequestosome-1 Protein, TOR Serine-Threonine Kinases
Abstract

The signaling adaptor p62 is a critical mediator of important cellular functions, owing to its ability to establish interactions with various signaling intermediaries. Here, we identify raptor as an interacting partner of p62. Thus, p62 is an integral part of the mTORC1 complex and is necessary to mediate amino acid signaling for the activation of S6K1 and 4EBP1. p62 interacts in an amino acid-dependent manner with mTOR and raptor. In addition, p62 binds the Rags proteins and favors formation of the active Rag heterodimer that is further stabilized by raptor. Interestingly, p62 colocalizes with Rags at the lysosomal compartment and is required for the interaction of mTOR with Rag GTPases in vivo and for translocation of the mTORC1 complex to the lysosome, a crucial step for mTOR activation.

DOI10.1016/j.molcel.2011.06.038
Alternate JournalMol Cell
PubMed ID21981924
PubMed Central IDPMC3190169
Grant ListR01CA134530 / CA / NCI NIH HHS / United States
R01CA132847 / CA / NCI NIH HHS / United States
Related Faculty: 
Jorge Moscat, Ph.D. Juan Francisco Linares Rodriguez, Ph.D. Maria Diaz-Meco Conde, Ph.D.

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