The molecular basis of integrated stress response silencing

Yang, Z.; Haakonsen, D.; Heider, M.; Witus, S. R.; Zelter, A.; Beschauner, T.; MacCoss, M. J.; Rape, M.

doi:10.1101/2024.12.02.626349

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bioRxiv · 10.1101/2024.12.02.626349

The molecular basis of integrated stress response silencing

Yang, Z.·Haakonsen, D.·Heider, M.·Witus, S. R.·Zelter, A.·Beschauner, T.·MacCoss, M. J.·Rape, M.

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Abstract

Chronic stress response activation impairs cell survival and causes devastating degenerative diseases. To counteract this, cells deploy dedicated silencing factors, such as the E3 ligase SIFI that terminates the mitochondrial stress response. How a single enzyme can sense stress across cells and elicit timely stress response inactivation is poorly understood. Here, we report the structure of human SIFI, which revealed how this 1.3MDa complex can target hundreds of proteins for accurate stress response silencing. SIFI attaches the first ubiquitin to substrates using flexible domains within an easily accessible scaffold, yet builds linkage-specific ubiquitin chains at distinct, sterically restricted elongation modules in its periphery. Ubiquitin handover via a ubiquitin-like domain couples versatile substrate modification to precise chain elongation. Stress response silencing therefore exploits a catalytic mechanism that is geared to process many diverse proteins and hence allows a single enzyme to monitor and, if appropriate, modulate a complex cellular state.

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Yang, Z., Haakonsen, D., Heider, M., Witus, S. R., Zelter, A., Beschauner, T., MacCoss, M. J., Rape, M.. 2024-12-02. The molecular basis of integrated stress response silencing. https://doi.org/10.1101/2024.12.02.626349

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