The conserved 3′X terminal domain of hepatitis C virus genomic RNA forms a two-stem structure that promotes viral RNA dimerization

被引:16
作者
Cantero-Camacho, Angel [1 ]
Gallego, Jose [1 ]
机构
[1] Univ Catolica Valencia, Fac Med, Valencia 46001, Spain
关键词
SECONDARY STRUCTURE; NONTRANSLATED REGION; 98-BASE SEQUENCE; HYDROGEN-BONDS; IN-VITRO; REPLICATION; ELEMENTS; NMR; END; TRANSLATION;
D O I
10.1093/nar/gkv786
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
The 3'X domain of hepatitis C virus is a strongly conserved structure located at the 3' terminus of the viral genomic RNA. This domain modulates the replication and translation processes of the virus in conjunction with an upstream 5BSL3.2 stem-loop, and contains a palindromic sequence that facilitates RNA dimerization. Based on nuclear magnetic resonance spectroscopy and gel electrophoresis, we report here that domain 3'X adopts a structure composed of two stem-loops, and not three hairpins or a mixture of folds, as previously proposed. This structure exposes unpaired terminal nucleotides after a double-helical stem and palindromic bases in an apical loop, favoring genomic RNA replication and self-association. At higher ionic strength the domain forms homodimers comprising an intermolecular duplex of 110 nucleotides. The 3'X sequences can alternatively form heterodimers with 5BSL3.2. This contact, reported to favor translation, likely involves local melting of one of the 3'X stem-loops.
引用
收藏
页码:8529 / 8539
页数:11
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