共 37 条
Inhibition of hepatitis delta virus RNA editing by short inhibitory RNA-mediated knockdown of ADAR1 but not ADAR2 expression
被引:51
作者:

Jayan, GC
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机构:
Georgetown Univ, Med Ctr, Div Mol Virol & Immunol, Rockville, MD 20850 USA Georgetown Univ, Med Ctr, Div Mol Virol & Immunol, Rockville, MD 20850 USA

Casey, JL
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机构:
Georgetown Univ, Med Ctr, Div Mol Virol & Immunol, Rockville, MD 20850 USA Georgetown Univ, Med Ctr, Div Mol Virol & Immunol, Rockville, MD 20850 USA
机构:
[1] Georgetown Univ, Med Ctr, Div Mol Virol & Immunol, Rockville, MD 20850 USA
关键词:
D O I:
10.1128/JVI.76.23.12399-12404.2002
中图分类号:
Q93 [微生物学];
学科分类号:
071005 ;
100705 ;
摘要:
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.
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页码:12399 / 12404
页数:6
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