Secondary Structure of Influenza A Virus Genomic Segment 8 RNA Folded in a Cellular Environment

被引:3
|
作者
Szutkowska, Barbara [1 ]
Wieczorek, Klaudia [1 ]
Kierzek, Ryszard [1 ]
Zmora, Pawel [1 ]
Peterson, Jake M. [2 ]
Moss, Walter N. [2 ]
Mathews, David H. [3 ,4 ]
Kierzek, Elzbieta [1 ]
机构
[1] Polish Acad Sci, Inst Bioorgan Chem, Noskowskiego 12-14, PL-61704 Poznan, Poland
[2] Iowa State Univ, Roy J Carver Dept Biochem, Biophys & Mol Biol, Ames, IA 50011 USA
[3] Univ Rochester, Dept Biochem & Biophys, Sch Med & Dent, 601 Elmwood Ave,Box 712, Rochester, NY 14642 USA
[4] Univ Rochester, Ctr RNA Biol, Sch Med & Dent, 601 Elmwood Ave,Box 712, Rochester, NY 14642 USA
关键词
influenza A virus; IAV; RNA virus; RNA secondary structure; RNA chemical mapping; AMANTADINE-RESISTANT; VIRAL-RNA; ANTISENSE OLIGONUCLEOTIDES; PROMOTER; MODEL; N-6-ALKYLADENOSINES; EPIDEMIOLOGY; ACTIVATION; STABILITY; FEATURES;
D O I
10.3390/ijms23052452
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Influenza A virus (IAV) is a member of the single-stranded RNA (ssRNA) family of viruses. The most recent global pandemic caused by the SARS-CoV-2 virus has shown the major threat that RNA viruses can pose to humanity. In comparison, influenza has an even higher pandemic potential as a result of its high rate of mutations within its relatively short (<13 kbp) genome, as well as its capability to undergo genetic reassortment. In light of this threat, and the fact that RNA structure is connected to a broad range of known biological functions, deeper investigation of viral RNA (vRNA) structures is of high interest. Here, for the first time, we propose a secondary structure for segment 8 vRNA (vRNA8) of A/California/04/2009 (H1N1) formed in the presence of cellular and viral components. This structure shows similarities with prior in vitro experiments. Additionally, we determined the location of several well-defined, conserved structural motifs of vRNA8 within IAV strains with possible functionality. These RNA motifs appear to fold independently of regional nucleoprotein (NP)-binding affinity, but a low or uneven distribution of NP in each motif region is noted. This research also highlights several accessible sites for oligonucleotide tools and small molecules in vRNA8 in a cellular environment that might be a target for influenza A virus inhibition on the RNA level.
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页数:24
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