RESETing ER proteostasis: selective stress pathway hidden in the secretory route |
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| Authors: | Andrés Couve Claudio Hetz |
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| Institution: | 1. Biomedical Neuroscience Institute, Faculty of Medicine, Universidad de Chile, , Santiago, Chile;2. Program of Physiology and Biophysics, Institute of Biomedical Sciences, Universidad de Chile, , Santiago, Chile;3. Program of Cellular and Molecular Biology, Center for Molecular Studies of the Cell, Institute of Biomedical Sciences, Universidad de Chile, , Santiago, Chile |
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| Abstract: | The efficient folding of membrane and secreted proteins relies on the unfolded protein response (UPR) to buffer fluctuations in the load of misfolded proteins. Although the UPR is thought to operate on a generic manner to maintain ER proteostasis, a recent study revealed the existence of a novel mechanism to eliminate misfolded GPI‐anchored proteins via the secretory pathway, termed ‘rapid ER stress‐induced export’ (RESET) (Satpute‐Krishnan et al, 2014 ). RESET involves the export of misfolded GPI proteins to the plasma membrane for subsequent degradation by the lysosome. |
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