TY - JOUR
T1 - Local structural changes of the influenza A virus ribonucleoprotein complex by single mutations in the specific residues involved in efficient genome packaging
AU - Takizawa, Naoki
AU - Ogura, Yoshitoshi
AU - Fujita, Yoko
AU - Noda, Takeshi
AU - Shigematsu, Hideki
AU - Hayashi, Tetsuya
AU - Kurokawa, Ken
N1 - Funding Information:
This work was supported by JSPS KAKENHI [ JP25871077 and JP15K21607 to N.T.]; and MEXT KAKENHI [ JP221S0002 to N.T., Y.O., T.H., and K.K.]. This research was partially supported by Platform Project for Supporting Drug Discovery and Life Science Research (Basis for Supporting Innovative Drug Discovery and Life Science Research (BINDS)) from AMED under Grant Number JP18am0101070 .
Publisher Copyright:
© 2019 Elsevier Inc.
PY - 2019/5
Y1 - 2019/5
N2 - The influenza A virus genome consists of eight single-stranded negative-sense RNA segments. The noncoding regions located at the 3′- and 5′- ends of each segment are necessary for genome packaging, and the terminal coding regions are required to precisely bundle the eight segments. However, the nucleotide residues important for genome bundling are not defined. Here, we introduced premature termination codons in the hemagglutinin (HA) or matrix protein 2 (M2) gene and constructed virus libraries containing random sequences in the terminal coding regions. Using these virus libraries, we identified nucleotide residues involved in efficient virus propagation. Viral genome packaging was impaired in viruses that contained single mutations at these identified residues. Furthermore, these single mutations altered the local structure of the viral ribonucleoprotein complex. Our results show that specific nucleotide residues in the viral protein coding region are involved in forming the precise structure of the viral ribonucleoprotein complex.
AB - The influenza A virus genome consists of eight single-stranded negative-sense RNA segments. The noncoding regions located at the 3′- and 5′- ends of each segment are necessary for genome packaging, and the terminal coding regions are required to precisely bundle the eight segments. However, the nucleotide residues important for genome bundling are not defined. Here, we introduced premature termination codons in the hemagglutinin (HA) or matrix protein 2 (M2) gene and constructed virus libraries containing random sequences in the terminal coding regions. Using these virus libraries, we identified nucleotide residues involved in efficient virus propagation. Viral genome packaging was impaired in viruses that contained single mutations at these identified residues. Furthermore, these single mutations altered the local structure of the viral ribonucleoprotein complex. Our results show that specific nucleotide residues in the viral protein coding region are involved in forming the precise structure of the viral ribonucleoprotein complex.
UR - http://www.scopus.com/inward/record.url?scp=85063113122&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85063113122&partnerID=8YFLogxK
U2 - 10.1016/j.virol.2019.03.004
DO - 10.1016/j.virol.2019.03.004
M3 - Article
C2 - 30875489
AN - SCOPUS:85063113122
SN - 0042-6822
VL - 531
SP - 126
EP - 140
JO - Virology
JF - Virology
ER -