PT  - JOURNAL ARTICLE
AU  - Jamie A. Kelly
AU  - Jonathan D. Dinman
TI  - Structural and functional conservation of the programmed -1 ribosomal frameshift signal of SARS-CoV-2
AID  - 10.1101/2020.03.13.991083
DP  - 2020 Jan 01
TA  - bioRxiv
PG  - 2020.03.13.991083
4099  - http://biorxiv.org/content/early/2020/03/15/2020.03.13.991083.short
4100  - http://biorxiv.org/content/early/2020/03/15/2020.03.13.991083.full
AB  - 17 years after the SARS-CoV epidemic, the world is facing the COVID-19 pandemic. COVID-19 is caused by a coronavirus named SARS-CoV-2. Given the most optimistic projections estimating that it will take more than a year to develop a vaccine, our best short term strategy may lie in identifying virus-specific targets for small molecule interventions. All coronaviruses utilize a molecular mechanism called -1 PRF to control the relative expression of their proteins. Prior analyses of SARS-CoV revealed that it utilizes a structurally unique three-stemmed mRNA pseudoknot to stimulate high rates of -1 PRF, that it also harbors a -1 PRF attenuation element. Altering -1 PRF activity negatively impacts virus replication, suggesting that this molecular mechanism may be therapeutically targeted. Here we present a comparative analysis of the original SARS-CoV and SARS-CoV-2 frameshift signals. Structural analyses reveal that the core -1 PRF signal, composed of the U UUA AAC slippery site and three-stemmed mRNA pseudoknot is highly conserved. In contrast, the upstream attenuator hairpin is less well conserved. Functional assays revealed that both elements promote similar rates of -1 PRF and that silent coding mutations in the slippery site strongly ablate -1 PRF activity. We suggest that molecules that were previously identified as inhibiting SARS-CoV mediated -1 PRF may serve as lead compounds to counter the current pandemic.