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Synthesis of a novel hepatitis C virus protein by ribosomal frameshift

Hepatitis C virus (HCV) is an important human pathogen that affects ∼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 synthe...

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Autores principales: Xu, Zhenming, Choi, Jinah, Yen, T.S.Benedict, Lu, Wen, Strohecker, Anne, Govindarajan, Sugantha, Chien, David, Selby, Mark J., Ou, Jing-hsiung
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2001
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC125543/
https://www.ncbi.nlm.nih.gov/pubmed/11447125
http://dx.doi.org/10.1093/emboj/20.14.3840
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author Xu, Zhenming
Choi, Jinah
Yen, T.S.Benedict
Lu, Wen
Strohecker, Anne
Govindarajan, Sugantha
Chien, David
Selby, Mark J.
Ou, Jing-hsiung
author_facet Xu, Zhenming
Choi, Jinah
Yen, T.S.Benedict
Lu, Wen
Strohecker, Anne
Govindarajan, Sugantha
Chien, David
Selby, Mark J.
Ou, Jing-hsiung
author_sort Xu, Zhenming
collection PubMed
description Hepatitis C virus (HCV) is an important human pathogen that affects ∼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.
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spelling pubmed-1255432002-09-19 Synthesis of a novel hepatitis C virus protein by ribosomal frameshift Xu, Zhenming Choi, Jinah Yen, T.S.Benedict Lu, Wen Strohecker, Anne Govindarajan, Sugantha Chien, David Selby, Mark J. Ou, Jing-hsiung EMBO J Article Hepatitis C virus (HCV) is an important human pathogen that affects ∼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. Oxford University Press 2001-07-16 /pmc/articles/PMC125543/ /pubmed/11447125 http://dx.doi.org/10.1093/emboj/20.14.3840 Text en Copyright © 2001 European Molecular Biology Organization
spellingShingle Article
Xu, Zhenming
Choi, Jinah
Yen, T.S.Benedict
Lu, Wen
Strohecker, Anne
Govindarajan, Sugantha
Chien, David
Selby, Mark J.
Ou, Jing-hsiung
Synthesis of a novel hepatitis C virus protein by ribosomal frameshift
title Synthesis of a novel hepatitis C virus protein by ribosomal frameshift
title_full Synthesis of a novel hepatitis C virus protein by ribosomal frameshift
title_fullStr Synthesis of a novel hepatitis C virus protein by ribosomal frameshift
title_full_unstemmed Synthesis of a novel hepatitis C virus protein by ribosomal frameshift
title_short Synthesis of a novel hepatitis C virus protein by ribosomal frameshift
title_sort synthesis of a novel hepatitis c virus protein by ribosomal frameshift
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC125543/
https://www.ncbi.nlm.nih.gov/pubmed/11447125
http://dx.doi.org/10.1093/emboj/20.14.3840
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