Dynamic RNA binding and unfolding by nonsense-mediated mRNA decay factor UPF2

Szeto, J.-Y. A.; Vivoli Vega, M.; Mailliot, J.; Orriss, G.; Sun, L.; Bufton, J. C.; Powers, K. T.; Yadav, S. K. N.; Berger, I.; Schaffitzel, C.

doi:10.1101/2024.10.26.620407

bioRxiv · 10.1101/2024.10.26.620407

Dynamic RNA binding and unfolding by nonsense-mediated mRNA decay factor UPF2

Szeto, J.-Y. A.·Vivoli Vega, M.·Mailliot, J.·Orriss, G.·Sun, L.·Bufton, J. C.·Powers, K. T.·Yadav, S. K. N.·Berger, I.·Schaffitzel, C.

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Abstract

Nonsense-mediated mRNA decay (NMD) is an mRNA surveillance pathway involved in translational control and gene expression regulation. Core NMD factors UPF1, UPF2 and UPF3B are conserved from yeast to humans and essential to target mcRNAs with a premature stop codon for decay. UPF2 binding to UPF1 activates UPF1s ATPase and helicase activities, and UPF2 binding to UPF3B is important for its association with the exon-junction complex and efficient NMD. However, UPF2s association with RNA remains largely uncharacterized. Here, we analyze nucleic acid binding, identifying the first and third MIF4G domains of UPF2 as main RNA-/DNA-binding modules. We find that UPF2s MIF4G domain-3 has RNA annealing activity while full-length UPF2 unfolds our reporter hairpin-RNA structure. We show that UPF2 preferentially binds and stabilizes single-stranded RNA (ss-RNA) in a sequence-independent manner. Concomitant to ss-RNA binding, UPF2 undergoes a distinct conformational change in its otherwise highly dynamic structure. UPF2s RNA binding and unfolding activity may support UPF1s helicase and mRNP remodeling activity and, in combination with UPF3B, stabilize UPF1s association with nonsense mRNA.

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Szeto, J.-Y. A., Vivoli Vega, M., Mailliot, J., Orriss, G., Sun, L., Bufton, J. C., Powers, K. T., Yadav, S. K. N., Berger, I., Schaffitzel, C.. 2024-10-28. Dynamic RNA binding and unfolding by nonsense-mediated mRNA decay factor UPF2. https://doi.org/10.1101/2024.10.26.620407

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