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bioRxiv · 10.1101/2024.07.30.605914

The integrated stress response regulates 18S nonfunctional rRNA decay in mammals

Coria, A. R.·Shah, A.·Shafieinour, M.·Taylor, S. J.·Guiblet, W.·Miller, J. T.·Mani Sharma, I.·Wu, C. C.-C.
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Abstract

18S nonfunctional rRNA decay (NRD) detects and eliminates translationally nonfunctional 18S rRNA. While this process is critical for ribosome quality control, the mechanisms underlying nonfunctional 18S rRNA turnover remain elusive. NRD was originally identified and has exclusively been studied in Saccharomyces cerevisiae. Here, we show that 18S NRD is conserved in mammals. Using genome-wide CRISPR genetic interaction screens, we find that mammalian NRD acts through the integrated stress response (ISR) via GCN2 and ribosomal protein ubiquitination by RNF10. Selective ribosome profiling reveals nonfunctional 18S rRNA induces translational arrest at start sites. Indeed, biochemical analyses demonstrate that ISR activation limits translation initiation and attenuates collisions between scanning 43S preinitiation complexes and nonfunctional 80S ribosomes arrested at start sites. Overall, the ISR promotes nonfunctional 18S rRNA and 40S ribosomal protein turnover by RNF10-mediated ubiquitination. These findings establish a dynamic feedback mechanism by which the GCN2-RNF10 axis surveils ribosome functionality at translation initiation.

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Coria, A. R., Shah, A., Shafieinour, M., Taylor, S. J., Guiblet, W., Miller, J. T., Mani Sharma, I., Wu, C. C.-C.. 2024-07-30. The integrated stress response regulates 18S nonfunctional rRNA decay in mammals. https://doi.org/10.1101/2024.07.30.605914

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