Towards elucidating the structure, function, and druggability of coronavirus cis-acting RNA motifs

Authors

  • Joanna Sztuba-Solinska Department of Biological Sciences, Auburn University, 120 W. Samford Ave, Rouse Life Sciences Building, Auburn, AL 36849, United States
  • Devadatta Gosavi Department of Biological Sciences, Auburn University, 120 W. Samford Ave, Rouse Life Sciences Building, Auburn, AL 36849, United States

DOI:

https://doi.org/10.18388/pb.2020_362

Abstract

Coronaviruses are the causative agents of mild to severe respiratory and intestinal infections
in humans. They are the largest RNA viruses, which genomes and encoded RNAs are known to fold into the highly-order structures that play essential roles in the viral replication and infectivity cycle. The recent outbreaks of new pathogenic coronaviruses steered researchersâ attention into the possibility of targeting their RNAs directly with novel RNA-specific drugs and therapeutic strategies. In this manuscript, we  highlight the recent biochemical and biophysical methodological advancements that yielded more in-depth insight into the structural and functional composition of coronaviruses cis-acting RNA motifs.
We discuss the complexity of these RNA regulatory elements, their intermolecular interactions,
post-transcriptional regulation, and their potential as druggable targets. We also indicate the location and function of unstructured and highly-conserved regions in coronaviruses RNA genomes representing viable aims for antisense oligonucleotide or CRISPR-based antiviral strategies.

Downloads

Download data is not yet available.

Published

2021-01-05