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Updated: Aug 6, 2026

A Protocol for Analyzing Hepatitis C Virus Replication
Published on: June 26, 2014
[Structure and function of the non-coding regions of hepatitis C viral RNA]
Mariola Dutkiewicz1, Agata Swiqtkowska, Jerzy Ciesiołka
1Pracownia Chemii i Biochemii RNA, Instytut Chemii Bioorganicznej PAN, ul. Noskowskiego 12/14, 61-704 Poznań.
Abstract:
At the 5' and 3' end of genomic HCV RNA there are two highly conserved, untranslated regions, 5'UTR and 3'UTR. These regions are organized into spatially ordered structures and they play key functions in regulation of processes of the viral life cycle. Most nucleotides of the region located at the 5' side of the coding sequence serve as an internal ribosomal entry site, IRES, which directs cap-independent translation. The RNA fragment present at the 3' end of the genome is required for virus replication and probably contributes to translation of viral proteins. During virus replication its genomic strand is transcribed into a strand of minus polarity, the replicative strand. Its 3' terminus is responsible for initiation of synthesis of descendant genomic strands. This article summarizes our current knowledge on the structure and function of the non-coding regions of hepatitis C genomic RNA, 5'UTR and 3'UTR, and the complementary sequences of the replicative viral strand.
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