Literature DB >> 11070008

Template requirements for RNA synthesis by a recombinant hepatitis C virus RNA-dependent RNA polymerase.

C C Kao1, X Yang, A Kline, Q M Wang, D Barket, B A Heinz.   

Abstract

The RNA-dependent RNA polymerase (RdRp) from hepatitis C virus (HCV), nonstructural protein 5B (NS5B), has recently been shown to direct de novo initiation using a number of complex RNA templates. In this study, we analyzed the features in simple RNA templates that are required to direct de novo initiation of RNA synthesis by HCV NS5B. NS5B was found to protect RNA fragments of 8 to 10 nucleotides (nt) from RNase digestion. However, NS5B could not direct RNA synthesis unless the template contained a stable secondary structure and a single-stranded sequence that contained at least one 3' cytidylate. The structure of a 25-nt template, named SLD3, was determined by nuclear magnetic resonance spectroscopy to contain an 8-bp stem and a 6-nt single-stranded sequence. Systematic analysis of changes in SLD3 revealed which features in the stem, loop, and 3' single-stranded sequence were required for efficient RNA synthesis. Also, chimeric molecules composed of DNA and RNA demonstrated that a DNA molecule containing a 3'-terminal ribocytidylate was able to direct RNA synthesis as efficiently as a sequence composed entirely of RNA. These results define the template sequence and structure sufficient to direct the de novo initiation of RNA synthesis by HCV RdRp.

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Year:  2000        PMID: 11070008      PMCID: PMC113194          DOI: 10.1128/jvi.74.23.11121-11128.2000

Source DB:  PubMed          Journal:  J Virol        ISSN: 0022-538X            Impact factor:   5.103


  44 in total

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Journal:  J Virol       Date:  1998-11       Impact factor: 5.103

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  61 in total

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6.  Evidence that the polymerase of respiratory syncytial virus initiates RNA replication in a nontemplated fashion.

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8.  Identification and functional characterization of the nascent RNA contacting residues of the hepatitis C virus RNA-dependent RNA polymerase.

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9.  Significance in replication of the terminal nucleotides of the flavivirus genome.

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10.  The Role of the Charged Residues of the GP2 Helical Regions in Ebola Entry().

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