Inhibition of hepatitis delta virus RNA editing by short inhibitory RNA-mediated knockdown of ADAR1 but not ADAR2 expression

J Virol. 2002 Dec;76(23):12399-404. doi: 10.1128/jvi.76.23.12399-12404.2002.

Abstract

Hepatitis delta virus (HDV) requires host RNA editing at the viral RNA amber/W site. Of the two host genes responsible for RNA editing via deamination of adenosines in double-stranded RNAs, short inhibitory RNA-mediated knockdown of host ADAR1 expression but not that of ADAR2 led to decreased HDV amber/W editing and virus production. Despite substantial sequence and structural variation among the amber/W sites of the three HDV genotypes, ADAR1a was primarily responsible for editing all three. We conclude that ADAR1 is primarily responsible for editing HDV RNA at the amber/W site during HDV infection.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adenosine Deaminase / genetics*
  • Adenosine Deaminase / metabolism
  • Alternative Splicing
  • Base Sequence
  • Cell Line
  • Gene Expression
  • Genotype
  • Hepatitis Delta Virus / genetics*
  • Hepatitis Delta Virus / pathogenicity
  • Hepatitis Delta Virus / physiology
  • Humans
  • RNA Editing*
  • RNA, Viral / genetics*
  • RNA, Viral / metabolism*
  • RNA-Binding Proteins
  • Transfection
  • Virus Replication

Substances

  • RNA, Viral
  • RNA-Binding Proteins
  • ADARB1 protein, human
  • Adenosine Deaminase