Why the study?
Many aspects of HCV RNA replication remain poorly understood, and most mechanistic studies on the RdRp NS5B have been conducted in vitro using isolated recombinant polymerase rather than in cellulo.
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Design
In cellulo replicon model study
Replicon model enables intracellular HCV NS5B studies; leaves open clinical translation of noncanonical initiation modes.
Many aspects of viral RNA replication of hepatitis C virus (HCV) are still poorly understood. The process of RNA synthesis is driven by the RNA-dependent RNA polymerase (RdRp) NS5B. Most mechanistic studies on NS5B so far were performed with in vitro systems using isolated recombinant polymerase. In this study, we present a replicon model, which allows the intracellular assessment of noncanonical modes of initiation by the full HCV replicase. Our results add to the understanding of the biochemical processes underlying initiation of RNA synthesis by NS5B by the discovery of internal initiation in cellulo . Moreover, they validate observations made in vitro , showing that the viral polymerase acts very similarly in isolation and in complex with other viral and host proteins. Finally, these observations provide clues about the evolution of RdRps of positive-strand RNA viruses, which might contain the intrinsic ability to initiate internally.
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Schult et al. (2019) studied this question.
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