Stress response silencing by an E3 ligase mutated in neurodegeneration by Diane L. Haakonsen & Michael Heider & Andrew J. Ingersoll & Kayla Vodehnal & Samuel R. Witus & Takeshi Uenaka & Marius Wernig & Michael Rapé ISBN 101038/S41586023069857 instant download

Stress response silencing by an E3 ligase mutated in neurodegeneration by Diane L. Haakonsen & Michael Heider & Andrew J. Ingersoll & Kayla Vodehnal & Samuel R. Witus & Takeshi Uenaka & Marius Wernig & Michael Rapé ISBN 101038/S41586023069857 instant download

Stress response pathways detect and alleviate adverse conditions to safeguard cell and tissue homeostasis, yet their prolonged activation induces apoptosis and disrupts organismal health1–3. How stress responses are turned of at the right time Check for updatesand place remains poorly understood. Here we report a ubiquitin-dependent mechanism that silences the cellular response to mitochondrial protein import stress. Crucial to this process is the silencing factor of the integrated stress response (SIFI), a large E3 ligase complex mutated in ataxia and in early-onset dementia that degrades both unimported mitochondrial precursors and stress response components. By recognizing bifunctional substrate motifs that equally encode protein localization and stability, the SIFI complex turns of a general stress response after a specifc stress event has been resolved. Pharmacological stress response silencing sustains cell survival even if stress resolution failed, which underscores the importance of signal termination and provides a roadmap for treating neurodegenerative diseases caused by mitochondrial import defects.