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PMID: 10679285 Published · ppublish English Journal Article

De novo RNA synthesis catalyzed by HCV RNA-dependent RNA polymerase.

Biochemical and biophysical research communications ·Vol. 268 ·No. 3 ·2000-02-24 ·Pages 798-803

Sun XL, Johnson RB, Hockman MA, Wang QM

Abstract

The 65 kDa RNA-dependent RNA polymerase (NS5B), encoded by the hepatitis C virus (HCV) genome, is a key component involved in viral replication. Here we provide the direct evidence that purified HCV polymerase catalyzed de novo RNA synthesis in a primer-independent manner using homopolymers and HCV RNA as templates. The enzyme could utilize both polyC and polyU as templates for de novo RNA synthesis, suggesting that NS5B specifically recognized pyrimidine bases for initiation. More importantly, NS5B also catalyzed de novo RNA synthesis with an HCV RNA template; the resulting nascent RNA products, smaller than the template used, contained ATP as the first nucleotide. These results indicate that the newly synthesized RNAs did not result from template self-priming and suggest that a replication initiation site in the HCV RNA genome is a uridylate.

MeSH Terms
3' Untranslated Regions Genome, Viral Hepacivirus/genetics,metabolism Poly C/metabolism Poly U/metabolism RNA, Viral/biosynthesis,genetics RNA-Dependent RNA Polymerase/metabolism Recombinant Proteins/metabolism Substrate Specificity Viral Nonstructural Proteins/metabolism
Chemicals
3' Untranslated Regions NS-5 protein, hepatitis C virus RNA, Viral Recombinant Proteins Viral Nonstructural Proteins Poly U Poly C RNA-Dependent RNA Polymerase
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Sun X L
Infectious Diseases Research, Lilly Research Laboratories, Indianapolis, Indiana 46285, USA.
Johnson R B
Hockman M A
Wang Q M
Article Info
Journal
Biochemical and biophysical research communications
Abbr.
Biochem Biophys Res Commun
ISSN
0006-291X
Published
2000-02-24
Pages
798-803
Language
English
Region
United States
NLM ID
0372516
Subset
IM
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