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通过短干扰RNA介导敲低ADAR1而非ADAR2的表达来抑制丁型肝炎病毒RNA编辑。

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

作者信息

Jayan Geetha C, Casey John L

机构信息

Division of Molecular Virology and Immunology, Georgetown University Medical Center, Rockville, Maryland 20850, USA.

出版信息

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

DOI:10.1128/jvi.76.23.12399-12404.2002
PMID:12414985
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC136899/
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.

摘要

丁型肝炎病毒(HDV)需要宿主对病毒RNA的琥珀色/W位点进行RNA编辑。在负责通过双链RNA中腺苷脱氨作用进行RNA编辑的两个宿主基因中,利用短发夹RNA介导的敲低宿主ADAR1而非ADAR2的表达,导致HDV琥珀色/W编辑和病毒产生减少。尽管三种HDV基因型的琥珀色/W位点存在大量序列和结构变异,但ADAR1a主要负责对所有三种进行编辑。我们得出结论,在HDV感染期间,ADAR1主要负责对HDV RNA的琥珀色/W位点进行编辑。

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本文引用的文献

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RNA editing in hepatitis delta virus genotype III requires a branched double-hairpin RNA structure.丁型肝炎病毒基因型III中的RNA编辑需要一种分支双发夹RNA结构。
J Virol. 2002 Aug;76(15):7385-97. doi: 10.1128/jvi.76.15.7385-7397.2002.
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Increased RNA editing and inhibition of hepatitis delta virus replication by high-level expression of ADAR1 and ADAR2.ADAR1和ADAR2的高水平表达增加RNA编辑并抑制丁型肝炎病毒复制。
J Virol. 2002 Apr;76(8):3819-27. doi: 10.1128/jvi.76.8.3819-3827.2002.
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Varied assembly and RNA editing efficiencies between genotypes I and II hepatitis D virus and their implications.丁型肝炎病毒I型和II型之间不同的组装及RNA编辑效率及其意义。
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Functional anatomy of siRNAs for mediating efficient RNAi in Drosophila melanogaster embryo lysate.用于在黑腹果蝇胚胎裂解物中介导高效RNA干扰的小干扰RNA的功能解剖学。
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J Virol. 2001 Sep;75(18):8547-55. doi: 10.1128/jvi.75.18.8547-8555.2001.
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