The role of the priming loop in influenza A virus RNA synthesis

被引:0
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作者
Te Velthuis A.J.W. [1 ,2 ]
Robb N.C. [2 ]
Kapanidis A.N. [2 ]
Fodor E. [1 ]
机构
[1] Sir William Dunn School of Pathology, University of Oxford, South Parks Road, Oxford
[2] Clarendon Laboratory, Department of Physics, University of Oxford, Parks Road, Oxford
基金
英国医学研究理事会; 英国生物技术与生命科学研究理事会;
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D O I
10.1038/nmicrobiol.2016.29
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摘要
RNA-dependent RNA polymerases (RdRps) are used by RNA viruses to replicate and transcribe their RNA genomes 1. They adopt a closed, right-handed fold with conserved subdomains called palm, fingers and thumb 1,2. Conserved RdRp motifs A-F coordinate the viral RNA template, NTPs and magnesium ions to facilitate nucleotide condensation 1. For the initiation of RNA synthesis, most RdRps use either a primer-dependent or de novo mechanism 3. The influenza A virus RdRp, in contrast, uses a capped RNA oligonucleotide to initiate transcription, and a combination of terminal and internal de novo initiation for replication 4. To understand how the influenza A virus RdRp coordinates these processes, we analysed the function of a thumb subdomain β-hairpin using initiation, elongation and single-molecule Förster resonance energy transfer (sm-FRET) assays. Our data indicate that this β-hairpin is essential for terminal initiation during replication, but not necessary for internal initiation and transcription. Analysis of individual residues in the tip of the β-hairpin shows that PB1 proline 651 is critical for efficient RNA synthesis in vitro and in cell culture. Overall, this work advances our understanding of influenza A virus RNA synthesis and identifies the initiation platform of viral replication. © 2016 Macmillan Publishers Limited. All rights reserved.
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