Transcriptional and epi-transcriptional dynamics of SARS-CoV-2 during cellular infection

Chang, Jessie J.-Y.; Rawlinson, Daniel; Pitt, Miranda E.; Taiaroa, George; Gleeson, Josie; Zhou, Chenxi; Mordant, Francesca L.; De Paoli-Iseppi, Ricardo; Caly, Leon; Purcell, Damian F.J.; Stinear, Tim P.; Londrigan, Sarah L.; Clark, Michael B.; Williamson, Deborah A.; Subbarao, Kanta; Coin, Lachlan J.M.

SARS-CoV-2 uses subgenomic (sg)RNA to produce viral proteins for replication and immune evasion. We applied long-read RNA and cDNA sequencing to in vitro human and primate infection models to study transcriptional dynamics. Transcription-regulating sequence (TRS)-dependent sgRNA was upregulated earlier in infection than TRS-independent sgRNA. An abundant class of TRS-independent sgRNA consisting of a portion of ORF1ab containing nsp1 joined to ORF10 and 3’UTR was upregulated at 48 hours post infection in human cell lines. We identified double-junction sgRNA containing both TRS-dependent and independent junctions. We found multiple sites at which the SARS-CoV-2 genome is consistently more modified than sgRNA, and that sgRNA modifications are stable across transcript clusters, host cells and time since infection. Our work highlights the dynamic nature of the SARS-CoV-2 transcriptome during its replication cycle. Our results are available via an interactive web-app at http://coinlab.mdhs.unimelb.edu.au/.