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Influenza B virus has global ordered RNA structure in (+) and (-) strands but relatively less stable predicted RNA folding free energy than allowed by the encoded protein sequence.

作者信息

Priore Salvatore F, Moss Walter N, Turner Douglas H

机构信息

Department of Chemistry and Center for RNA Biology, University of Rochester, Rochester, NY 14627-0216, USA.

出版信息

BMC Res Notes. 2013 Aug 19;6:330. doi: 10.1186/1756-0500-6-330.

Abstract

BACKGROUND

Influenza A virus contributes to seasonal epidemics and pandemics and contains Global Ordered RNA structure (GORS) in the nucleoprotein (NP), non-structural (NS), PB2, and M segments. A related virus, influenza B, is also a major annual public health threat, but unlike influenza A is very selective to human hosts. This study extends the search for GORS to influenza B.

FINDINGS

A survey of all available influenza B sequences reveals GORS in the (+) and (-)RNAs of the NP, NS, PB2, and PB1 gene segments. The results are similar to influenza A, except GORS is observed for the M1 segment of influenza A but not for PB1. In general, the folding free energies of human-specific influenza B RNA segments are less stable than allowable by the encoded amino acid sequence. This is consistent with findings in influenza A, where human-specific influenza RNA folds are less stable than avian and swine strains.

CONCLUSIONS

These results reveal fundamental molecular similarities and differences between Influenza A and B and suggest a rational basis for choosing segments to target with therapeutics and for viral attenuation for live vaccines by altering RNA folding stability.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ee3/3765861/e1717c88e0c6/1756-0500-6-330-1.jpg

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