Protein-protein interactions with G3BPs drive stress granule condensation and gene expression changes under cellular stress

Liboy-Lugo, J. M.; Espinoza, C. A.; Sheu-Gruttadauria, J.; Park, J. E.; Xu, A.; Jowhar, Z.; Gao, A. L.; Carmona-Negron, J. A.; Wittmann, T.; Jura, N.; Floor, S. N.

doi:10.1101/2024.02.06.579149

bioRxiv · 10.1101/2024.02.06.579149

Protein-protein interactions with G3BPs drive stress granule condensation and gene expression changes under cellular stress

Liboy-Lugo, J. M.·Espinoza, C. A.·Sheu-Gruttadauria, J.·Park, J. E.·Xu, A.·Jowhar, Z.·Gao, A. L.·Carmona-Negron, J. A.·Wittmann, T.·Jura, N.·Floor, S. N.

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Abstract

Stress granules (SGs) are macromolecular assemblies that form under cellular stress. Formation of these condensates is driven by the condensation of RNA and RNA-binding proteins such as G3BPs. G3BPs condense into SGs following stress-induced translational arrest. Three G3BP paralogs (G3BP1, G3BP2A, and G3BP2B) have been identified in vertebrates. However, the contribution of different G3BP paralogs to stress granule formation and stress-induced gene expression changes is incompletely understood. Here, we identified key residues for G3BP condensation such as V11. This conserved amino acid is required for formation of the G3BP-Caprin-1 complex, hence promoting SG assembly. Total RNA sequencing and ribosome profiling revealed that disruption of G3BP condensation corresponds to changes in mRNA levels and ribosome engagement during the integrated stress response (ISR). Moreover, we found that G3BP2B preferentially condenses and promotes changes in mRNA expression under endoplasmic reticulum (ER) stress. Together, this work suggests that stress granule assembly promotes changes in gene expression under cellular stress, which is differentially regulated by G3BP paralogs.

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Liboy-Lugo, J. M., Espinoza, C. A., Sheu-Gruttadauria, J., Park, J. E., Xu, A., Jowhar, Z., Gao, A. L., Carmona-Negron, J. A., Wittmann, T., Jura, N., Floor, S. N.. 2024-02-07. Protein-protein interactions with G3BPs drive stress granule condensation and gene expression changes under cellular stress. https://doi.org/10.1101/2024.02.06.579149

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