Synthesis of a novel hepatitis C virus protein by ribosomal frameshift

被引:217
作者
Xu, ZM
Choi, J
Yen, TSB
Lu, W
Strohecker, A
Govindarajan, S
Chien, D
Selby, MJ
Ou, JH
机构
[1] Univ So Calif, Dept Mol Microbiol & Immunol, Los Angeles, CA 90033 USA
[2] Univ Calif San Francisco, Dept Pathol, San Francisco, CA 94121 USA
[3] Vet Affairs Med Ctr, Pathol Serv, San Francisco, CA 94121 USA
[4] Univ So Calif, Dept Pathol, Downey, CA 90242 USA
[5] Rancho Los Amigos Med Ctr, Downey, CA 90242 USA
[6] Chiron Corp, Emeryville, CA 94608 USA
关键词
HCV core protein; HCVF protein; hepatitis C virus; ribosomal frameshift;
D O I
10.1093/emboj/20.14.3840
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
Hepatitis C virus (HCV) is an important human pathogen that affects similar to 100 million people worldwide. Its RNA genome codes for a polyprotein, which is cleaved by viral and cellular proteases to produce at least 10 mature viral protein products. We report here the discovery of a novel HCV protein synthesized by ribosomal frameshift. This protein, which we named the F protein, is synthesized from the initiation codon of the polyprotein sequence followed by ribosomal frameshift into the -2/+1 reading frame. This ribosomal frameshift requires only codons 8-14 of the core protein-coding sequence, and the shift junction is located at or near codon 11. An F protein analog synthesized in vitro reacted with the sera of HCV patients but not with the sera of hepatitis B patients, indicating the expression of the F protein during natural HCV infection. This unexpected finding may open new avenues for the development of anti-HCV drugs.
引用
收藏
页码:3840 / 3848
页数:9
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