4.8 Article

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

Journal

ELIFE
Volume 6, Issue -, Pages -

Publisher

ELIFE SCIENCES PUBLICATIONS LTD
DOI: 10.7554/eLife.27453

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Funding

  1. Wellcome [103068/Z/13/Z]
  2. Leverhulme Trust [ECF/019/2013]
  3. Deutsche Forschungsge meinschaft [SFB1032]
  4. Engineering and Physical Sciences Research Council [EP/K028286/1] Funding Source: researchfish
  5. Wellcome Trust [103068/Z/13/Z] Funding Source: Wellcome Trust
  6. EPSRC [EP/K028286/1] Funding Source: UKRI

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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 nonstructural 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.

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