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Protein-mediated RNA folding governs sequence-specific interactions between rotavirus genome segments
被引:61
作者:

Borodavka, Alexander
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机构:
Univ Leeds, Sch Mol & Cellular Biol, Astbury Ctr Struct Mol Biol, Leeds, W Yorkshire, England
Ludwig Maximilian Univ Munich, Ctr NanoSci, Dept Chem, NIM, Munich, Germany
Ludwig Maximilian Univ Munich, CiPSM, Munich, Germany Univ Leeds, Sch Mol & Cellular Biol, Astbury Ctr Struct Mol Biol, Leeds, W Yorkshire, England

Dykeman, Eric C.
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Univ York, York Ctr Complex Syst Anal, York, N Yorkshire, England
Univ York, Dept Math, York, N Yorkshire, England
Univ York, Dept Biol, York, N Yorkshire, England Univ Leeds, Sch Mol & Cellular Biol, Astbury Ctr Struct Mol Biol, Leeds, W Yorkshire, England

Schrimpf, Waldemar
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机构:
Ludwig Maximilian Univ Munich, Ctr NanoSci, Dept Chem, NIM, Munich, Germany
Ludwig Maximilian Univ Munich, CiPSM, Munich, Germany Univ Leeds, Sch Mol & Cellular Biol, Astbury Ctr Struct Mol Biol, Leeds, W Yorkshire, England

Lamb, Don C.
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机构:
Ludwig Maximilian Univ Munich, Ctr NanoSci, Dept Chem, NIM, Munich, Germany
Ludwig Maximilian Univ Munich, CiPSM, Munich, Germany Univ Leeds, Sch Mol & Cellular Biol, Astbury Ctr Struct Mol Biol, Leeds, W Yorkshire, England
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
来源:
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.
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