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

被引:61
作者
Borodavka, Alexander [1 ,2 ,3 ]
Dykeman, Eric C. [4 ,5 ,6 ]
Schrimpf, Waldemar [2 ,3 ]
Lamb, Don C. [2 ,3 ]
机构
[1] Univ Leeds, Sch Mol & Cellular Biol, Astbury Ctr Struct Mol Biol, Leeds, W Yorkshire, England
[2] Ludwig Maximilian Univ Munich, Ctr NanoSci, Dept Chem, NIM, Munich, Germany
[3] Ludwig Maximilian Univ Munich, CiPSM, Munich, Germany
[4] Univ York, York Ctr Complex Syst Anal, York, N Yorkshire, England
[5] Univ York, Dept Math, York, N Yorkshire, England
[6] Univ York, Dept Biol, York, N Yorkshire, England
基金
英国工程与自然科学研究理事会; 英国惠康基金;
关键词
INFLUENZA-A VIRUS; MESSENGER-RNAS; IN-VITRO; REPLICATION; VP1; ORGANIZATION; TOOL;
D O I
10.7554/eLife.27453
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
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.
引用
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页数:22
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