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      Wolfram syndrome 1 gene negatively regulates ER stress signaling in rodent and human cells.

      The Journal of clinical investigation
      Activating Transcription Factor 6, genetics, metabolism, Animals, COS Cells, Calmodulin-Binding Proteins, Cell Line, Tumor, Cercopithecus aethiops, Endoplasmic Reticulum, pathology, Gene Expression Regulation, Humans, Insulin-Secreting Cells, Membrane Proteins, Mice, Proteasome Endopeptidase Complex, Rats, Signal Transduction, Trans-Activators, Ubiquitin, Ubiquitin-Protein Ligases, Ubiquitination, Unfolded Protein Response, Wolfram Syndrome

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          Abstract

          Wolfram syndrome is an autosomal-recessive disorder characterized by insulin-dependent diabetes mellitus, caused by nonautoimmune loss of beta cells, and neurological dysfunctions. We have previously shown that mutations in the Wolfram syndrome 1 (WFS1) gene cause Wolfram syndrome and that WFS1 has a protective function against ER stress. However, it remained to be determined how WFS1 mitigates ER stress. Here we have shown in rodent and human cell lines that WFS1 negatively regulates a key transcription factor involved in ER stress signaling, activating transcription factor 6alpha (ATF6alpha), through the ubiquitin-proteasome pathway. WFS1 suppressed expression of ATF6alpha target genes and repressed ATF6alpha-mediated activation of the ER stress response element (ERSE) promoter. Moreover, WFS1 stabilized the E3 ubiquitin ligase HRD1, brought ATF6alpha to the proteasome, and enhanced its ubiquitination and proteasome-mediated degradation, leading to suppression of ER stress signaling. Consistent with these data, beta cells from WFS1-deficient mice and lymphocytes from patients with Wolfram syndrome exhibited dysregulated ER stress signaling through upregulation of ATF6alpha and downregulation of HRD1. These results reveal a role for WFS1 in the negative regulation of ER stress signaling and in the pathogenesis of diseases involving chronic, unresolvable ER stress, such as pancreatic beta cell death in diabetes.

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