Mapping of the influenza A virus genome RNA structure and interactions reveals essential elements of viral replication

被引:3
|
作者
Yang, Rui [1 ]
Pan, Minglei [2 ]
Guo, Jiamei [3 ]
Huang, Yong [1 ]
Zhang, Qiangfeng Cliff [1 ]
Deng, Tao [2 ,3 ]
Wang, Jianwei [4 ,5 ]
机构
[1] Tsinghua Univ, Tsinghua Univ Peking Univ Joint Ctr Life Sci, Sch Life Sci, Beijing Frontier Res Ctr Biol Struct,State Key Lab, Beijing 100084, Peoples R China
[2] Chinese Acad Med Sci & Peking Union Med Coll, Inst Pathogen Biol, NHC Key Lab Syst Biol Pathogens, Beijing 100730, Peoples R China
[3] Chinese Acad Sci, Inst Microbiol, CAS Key Lab Pathogen Microbiol & Immunol, Beijing 100101, Peoples R China
[4] Chinese Acad Med Sci & Peking Union Med Coll, Inst Pathogen Biol, NHC Key Lab Syst Biol Pathogens & Christophe Meri, Beijing, Peoples R China
[5] Chinese Acad Med Sci & Peking Union Med Coll, Key Lab Resp Dis Pathogen, Beijing 100730, Peoples R China
来源
CELL REPORTS | 2024年 / 43卷 / 03期
基金
中国国家自然科学基金;
关键词
SECONDARY STRUCTURE; PACKAGING SIGNALS; NONCODING REGIONS; LIVING CELLS; PA SUBUNIT; SEGMENT; 7; IN-VIVO; GENERATION; BINDING; PB2;
D O I
10.1016/j.celrep.2024.113833
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Influenza A virus (IAV) represents a constant public health threat. The single -stranded, segmented RNA genome of IAV is replicated in host cell nuclei as a series of 8 ribonucleoprotein complexes (vRNPs) with RNA structures known to exert essential function to support viral replication. Here, we investigate RNA secondary structures and RNA interactions networks of the IAV genome and construct an in vivo structure model for each of the 8 IAV genome segments. Our analyses reveal an overall in vivo and in virio resemblance of the IAV genome conformation but also wide disparities among long-range and intersegment interactions. Moreover, we identify a longrange RNA interaction that exerts an essential role in genome packaging. Disrupting this structure displays reduced infectivity, attenuating virus pathogenicity in mice. Our findings characterize the in vivo RNA structural landscape of the IAV genome and reveal viral RNA structures that can be targeted to develop antiviral interventions.
引用
收藏
页数:24
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