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bioRxiv · 10.1101/2021.02.17.431652

How the replication and transcription complex of SARS-CoV-2 functions in leader-to-body fusion

Li, X.·Zhao, Q.·Chang, J.·Duan, G.·Bei, J.·Yau, T. O.·Yang, J.·Ruan, J.·He, B.·Shan, G.
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Abstract

BackgroundCoronavirus disease 2019 (COVID-19) is caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Although unprecedented efforts are underway to develop therapeutic strategies against this disease, scientists have acquired only a little knowledge regarding the structures and functions of the CoV replication and transcription complex (RTC) and 16 non-structural proteins, named NSP1-16. ResultsIn the present study, we proposed a two-route model to answer how the RTC functions in the jumping transcription of CoVs. The key step leading to this model was that the motif AAACH for METTL3 recognition flanking the transcription regulatory sequence (TRS) motif was discovered to determine the m6A methylation of SARS-CoV-2 RNAs, by reanalyzing public Nanopore RNA-seq data. As the most important finding, TRS hairpins were reported for the first time to interpret NSP15 cleavage, RNA methylation of CoVs and their association at the molecular level. In addition, we reported canonical TRS motifs of all CoVs to prove the importance of our findings. ConclusionsThe main conclusions are: (1) TRS hairpins can be used to identify recombination regions in CoV genomes; (2) RNA methylation of CoVs participates in the determination of the RNA secondary structures by affecting the formation of base pairing; and (3) The eventual determination of the CoV RTC global structure needs to consider METTL3 in the experimental design. Our findings enrich fundamental knowledge in the field of gene expression and its regulation, providing a crucial basis for future studies.

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Li, X., Zhao, Q., Chang, J., Duan, G., Bei, J., Yau, T. O., Yang, J., Ruan, J., He, B., Shan, G.. 2021-02-17. How the replication and transcription complex of SARS-CoV-2 functions in leader-to-body fusion. https://doi.org/10.1101/2021.02.17.431652

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