Molecular Basis of the Rapamycin Insensitivity of Target Of Rapamycin Complex 2.
Target of Rapamycin (TOR) plays central roles in the regulation of eukaryote growth as the hub of two essential multiprotein complexes: TORC1, which is rapamycin-sensitive, and the lesser characterized TORC2, which is not. TORC2 is a key regulator of lipid biosynthesis and Akt-mediated survival signaling. In spite of its importance, ... its structure and the molecular basis of its rapamycin insensitivity are unknown. Using crosslinking-mass spectrometry and electron microscopy, we determined the architecture of TORC2. TORC2 displays a rhomboid shape with pseudo-2-fold symmetry and a prominent central cavity. Our data indicate that the C-terminal part of Avo3, a subunit unique to TORC2, is close to the FKBP12-rapamycin-binding domain of Tor2. Removal of this sequence generated a FKBP12-rapamycin-sensitive TORC2 variant, which provides a powerful tool for deciphering TORC2 function in vivo. Using this variant, we demonstrate a role for TORC2 in G2/M cell-cycle progression.
Mesh Terms:
Antifungal Agents, Binding Sites, Biocatalysis, Blotting, Western, Carrier Proteins, Cell Cycle, Cell Cycle Proteins, Drug Resistance, Mass Spectrometry, Microscopy, Electron, Multiprotein Complexes, Mutation, Phosphatidylinositol 3-Kinases, Protein Structure, Tertiary, Saccharomyces cerevisiae, Saccharomyces cerevisiae Proteins, Sirolimus, TOR Serine-Threonine Kinases
Antifungal Agents, Binding Sites, Biocatalysis, Blotting, Western, Carrier Proteins, Cell Cycle, Cell Cycle Proteins, Drug Resistance, Mass Spectrometry, Microscopy, Electron, Multiprotein Complexes, Mutation, Phosphatidylinositol 3-Kinases, Protein Structure, Tertiary, Saccharomyces cerevisiae, Saccharomyces cerevisiae Proteins, Sirolimus, TOR Serine-Threonine Kinases
Mol. Cell
Date: Jun. 18, 2015
PubMed ID: 26028537
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