Lee Nara, Le Sage Valerie, Nanni Adalena V, Snyder Dan J, Cooper Vaughn S, Lakdawala Seema S
University of Pittsburgh School of Medicine, Department of Microbiology and Molecular Genetics, 450 Technology Drive, Pittsburgh, PA 15219, USA.
Nucleic Acids Res. 2017 Sep 6;45(15):8968-8977. doi: 10.1093/nar/gkx584.
Influenza A virus (IAV) genomes are composed of eight single-stranded RNA segments that are coated by viral nucleoprotein (NP) molecules. Classically, the interaction between NP and viral RNA (vRNA) is depicted as a uniform pattern of 'beads on a string'. Using high-throughput sequencing of RNA isolated by crosslinking immunoprecipitation (HITS-CLIP), we identified the vRNA binding profiles of NP for two H1N1 IAV strains in virions. Contrary to the prevailing model for vRNA packaging, NP does not bind vRNA uniformly in the A/WSN/1933 and A/California/07/2009 strains, but instead each vRNA segment exhibits a unique binding profile, containing sites that are enriched or poor in NP association. Intriguingly, both H1N1 strains have similar yet distinct NP binding profiles despite extensive sequence conservation. Peaks identified by HITS-CLIP were verified as true NP binding sites based on insensitivity to DNA antisense oligonucleotide-mediated RNase H digestion. Moreover, nucleotide content analysis of NP peaks revealed that these sites are relatively G-rich and U-poor compared to the genome-wide nucleotide content, indicating an as-yet unidentified sequence bias for NP association in vivo. Taken together, our genome-wide study of NP-vRNA interaction has implications for the understanding of influenza vRNA architecture and genome packaging.
甲型流感病毒(IAV)基因组由八个单链RNA片段组成,这些片段被病毒核蛋白(NP)分子包裹。传统上,NP与病毒RNA(vRNA)之间的相互作用被描述为“串珠”的均匀模式。通过交联免疫沉淀分离RNA的高通量测序(HITS-CLIP),我们确定了病毒粒子中两种H1N1 IAV毒株的NP的vRNA结合谱。与普遍的vRNA包装模型相反,在A/WSN/1933和A/California/07/2009毒株中,NP并非均匀地结合vRNA,而是每个vRNA片段都呈现出独特的结合谱,包含NP结合丰富或稀少的位点。有趣的是,尽管序列高度保守,但两种H1N1毒株具有相似但又不同的NP结合谱。基于对DNA反义寡核苷酸介导的RNase H消化不敏感,HITS-CLIP鉴定出的峰被确认为真正的NP结合位点。此外,NP峰的核苷酸含量分析表明,与全基因组核苷酸含量相比,这些位点相对富含G且缺乏U,这表明体内NP结合存在尚未确定的序列偏好。综上所述,我们对NP-vRNA相互作用的全基因组研究有助于理解流感vRNA结构和基因组包装。