| Literature DB >> 26876939 |
Young Sung Yun1, Kwan Hyun Kim1, Barbara Tschida2, Zohar Sachs3, Klara E Noble-Orcutt4, Branden S Moriarity5, Teng Ai6, Rui Ding6, Jessica Williams6, Liqiang Chen6, David Largaespada7, Do-Hyung Kim8.
Abstract
Reduction of translational fidelity often occurs in cells with high rates of protein synthesis, generating defective ribosomal products. If not removed, such aberrant proteins can be a major source of cellular stress causing human diseases. Here, we demonstrate that mTORC1 promotes the formation of immunoproteasomes for efficient turnover of defective proteins and cell survival. mTORC1 sequesters precursors of immunoproteasome β subunits via PRAS40. When activated, mTORC1 phosphorylates PRAS40 to enhance protein synthesis and simultaneously to facilitate the assembly of the β subunits for forming immunoproteasomes. Consequently, the PRAS40 phosphorylations play crucial roles in clearing aberrant proteins that accumulate due to mTORC1 activation. Mutations of RAS, PTEN, and TSC1, which cause mTORC1 hyperactivation, enhance immunoproteasome formation in cells and tissues. Those mutations increase cellular dependence on immunoproteasomes for stress response and survival. These results define a mechanism by which mTORC1 couples elevated protein synthesis with immunoproteasome biogenesis to protect cells against protein stress.Entities:
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Year: 2016 PMID: 26876939 PMCID: PMC4870089 DOI: 10.1016/j.molcel.2016.01.013
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 17.970