Protein-mediated RNA folding governs sequence-specific interactions between rotavirus genome segments

Elife. 2017 Sep 18:6:e27453. doi: 10.7554/eLife.27453.

Abstract

Segmented RNA viruses are ubiquitous pathogens, which include influenza viruses and rotaviruses. A major challenge in understanding their assembly is the combinatorial problem of a non-random selection of a full genomic set of distinct RNAs. This process involves complex RNA-RNA and protein-RNA interactions, which are often obscured by non-specific binding at concentrations approaching in vivo assembly conditions. Here, we present direct experimental evidence of sequence-specific inter-segment interactions between rotavirus RNAs, taking place in a complex RNA- and protein-rich milieu. We show that binding of the rotavirus-encoded non-structural protein NSP2 to viral ssRNAs results in the remodeling of RNA, which is conducive to formation of stable inter-segment contacts. To identify the sites of these interactions, we have developed an RNA-RNA SELEX approach for mapping the sequences involved in inter-segment base-pairing. Our findings elucidate the molecular basis underlying inter-segment interactions in rotaviruses, paving the way for delineating similar RNA-RNA interactions that govern assembly of other segmented RNA viruses.

Keywords: Fluorescence Cross-Correlation Spectroscopy; RNA folding; RNA-RNA interactions; Rotavirus; Virus assembly; biophysics; infectious disease; microbiology; structural biology; virus.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Genome, Viral*
  • Nucleic Acid Conformation
  • Protein Binding
  • RNA Folding*
  • RNA, Viral / genetics
  • RNA, Viral / metabolism*
  • RNA-Binding Proteins / metabolism*
  • Rotavirus / genetics*
  • Rotavirus / physiology
  • Viral Nonstructural Proteins / metabolism*

Substances

  • RNA, Viral
  • RNA-Binding Proteins
  • Viral Nonstructural Proteins
  • NS35 protein, rotavirus