cis-acting signals in encapsidation of hantaan virus S-segment viral genomic RNA by its N protein

被引:47
作者
Severson, WE
Xu, XL
Jonsson, CB
机构
[1] New Mexico State Univ, Dept Chem & Biochem, Las Cruces, NM 88003 USA
[2] New Mexico State Univ, Grad Program Mol Biol, Las Cruces, NM 88003 USA
关键词
D O I
10.1128/JVI.75.6.2646-2652.2001
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The nucleocapsid (N) protein encapsidates both viral genomic RNA (vRNA) and the antigenomic RNA (cRNA), but not viral mRNA, Previous work has shown that the N protein has preference for vRNA, and this suggested the possibility of a cis-acting signal that could be used to initiate encapsidation for the S segment, To map the cis-acting determinants, several deletion RNA derivatives and synthetic oligoribonucleotides were constructed from the S segment of the Hantaan virus (HTNV) VRNA, N protein-RNA interactions were examined by UV cross-linking studies, filter-binding assays, and gel electrophoresis mobility shift assays to define the ability of each to bind HTNV N protein. The 5' end of the S-segment vRNA was observed to be necessary and sufficient for the binding reaction. Modeling of the 5' end of the vRNA revealed a possible stem-loop structure (SL) with a large single-stranded loop. We suggest that a specific interaction occurs between the N protein and sequences within this region to initiate encapsidation of the vRNAs.
引用
收藏
页码:2646 / 2652
页数:7
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