Hepatitis B Virus X and Regulation of Viral Gene Expression

Cold Spring Harb Perspect Med. 2016 Jan 8;6(3):a021402. doi: 10.1101/cshperspect.a021402.

Abstract

The efficient replication of hepatitis B virus (HBV) requires the HBV regulatory hepatitis B virus X (HBx) protein. The exact contributions of HBx are not fully understood, in part because of the limitations of the assays used for its study. When HBV replication is driven from a plasmid DNA, the contribution of HBx is modest. However, there is an absolute requirement for HBx in assays that recapitulate the infectious virus life cycle. There is much evidence that HBx can contribute directly to HBV replication by acting on viral promoters embedded within protein coding sequences. In addition, HBx may also contribute indirectly by modulating cellular pathways to benefit virus replication. Understanding the mechanism(s) of HBx action during virus replication may provide insight into novel ways to disrupt chronic HBV replication.

Publication types

  • Review

MeSH terms

  • DNA Replication*
  • DNA, Viral / metabolism*
  • Gene Expression*
  • Genome, Viral
  • Hepatitis B virus / genetics*
  • Hepatitis B virus / physiology
  • Hepatitis B virus / ultrastructure
  • Humans
  • Trans-Activators / metabolism*
  • Trans-Activators / ultrastructure
  • Viral Regulatory and Accessory Proteins
  • Virus Replication

Substances

  • DNA, Viral
  • Trans-Activators
  • Viral Regulatory and Accessory Proteins
  • hepatitis B virus X protein