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      CHOP induces death by promoting protein synthesis and oxidation in the stressed endoplasmic reticulum.

      Genes & development

      toxicity, Tunicamycin, physiology, metabolism, Transcription Factors, Transcription Factor CHOP, Reverse Transcriptase Polymerase Chain Reaction, Protein Phosphatase 1, Protein Biosynthesis, Neoplasm Proteins, Mice, chemically induced, Kidney Tubular Necrosis, Acute, pathology, Kidney, Immunoprecipitation, Immunoblotting, Gene Expression Regulation, Fibroblasts, Eukaryotic Initiation Factor-2, Endoplasmic Reticulum, Cell Death, Cell Cycle Proteins, Caenorhabditis elegans, CCAAT-Enhancer-Binding Proteins, Antigens, Differentiation, Animals, Analysis of Variance

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          Unfolded and malfolded client proteins impose a stress on the endoplasmic reticulum (ER), which contributes to cell death in pathophysiological conditions. The transcription factor C/EBP homologous protein (CHOP) is activated by ER stress, and CHOP deletion protects against its lethal consequences. We find that CHOP directly activates GADD34, which promotes ER client protein biosynthesis by dephosphorylating phospho-Ser 51 of the alpha-subunit of translation initiation factor 2 (eIF2alpha) in stressed cells. Thus, impaired GADD34 expression reduces client protein load and ER stress in CHOP(-/-) cells exposed to perturbations that impair ER function. CHOP(-/-) and GADD34 mutant cells accumulate less high molecular weight protein complexes in their stressed ER than wild-type cells. Furthermore, mice lacking GADD34-directed eIF2alpha dephosphorylation, like CHOP(-/-) mice, are resistant to renal toxicity of the ER stress-inducing drug tunicamycin. CHOP also activates ERO1alpha, which encodes an ER oxidase. Consequently, the ER of stressed CHOP(-/-) cells is relatively hypo-oxidizing. Pharmacological and genetic manipulations that promote a hypo-oxidizing ER reduce abnormal high molecular weight protein complexes in the stressed ER and protect from the lethal consequences of ER stress. CHOP deletion thus protects cells from ER stress by decreasing ER client protein load and changing redox conditions within the organelle.

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