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通过诱导型DCL-2依赖性途径在栗疫病菌中产生的低病毒衍生小RNA的特征分析。

Characterization of hypovirus-derived small RNAs generated in the chestnut blight fungus by an inducible DCL-2-dependent pathway.

作者信息

Zhang Xuemin, Segers Gert C, Sun Qihong, Deng Fuyou, Nuss Donald L

机构信息

Center for Biosystems Research, University of Maryland Biotechnology Institute, Shady Grove Campus, 9600 Gudelsky Dr., Rockville, MD 20850, USA.

出版信息

J Virol. 2008 Mar;82(6):2613-9. doi: 10.1128/JVI.02324-07. Epub 2008 Jan 16.

Abstract

The disruption of one of two dicer genes, dcl-2, of the chestnut blight fungus Cryphonectria parasitica was recently shown to increase susceptibility to mycovirus infection (G. C. Segers, X. Zhang, F. Deng, Q. Sun, and D. L. Nuss, Proc. Natl. Acad. Sci. USA 104:12902-12906, 2007). We now report the accumulation of virus-derived small RNAs (vsRNAs) in hypovirus CHV1-EP713-infected wild-type and dicer gene dcl-1 mutant C. parasitica strains but not in hypovirus-infected dcl-2 mutant and dcl-1 dcl-2 double-mutant strains. The CHV1-EP713 vsRNAs were produced from both the positive and negative viral RNA strands at a ratio of 3:2 in a nonrandom distribution along the viral genome. We also show that C. parasitica responds to hypovirus and mycoreovirus infections with a significant increase (12- to 20-fold) in dcl-2 expression while the expression of dcl-1 is increased only modestly (2-fold). The expression of dcl-2 is further increased ( approximately 35-fold) following infection with a hypovirus CHV1-EP713 mutant that lacks the p29 suppressor of RNA silencing. The combined results demonstrate the biogenesis of mycovirus-derived small RNAs in a fungal host through the action of a specific dicer gene, dcl-2. They also reveal that dcl-2 expression is significantly induced in response to mycovirus infection by a mechanism that appears to be repressed by the hypovirus-encoded p29 suppressor of RNA silencing.

摘要

最近研究表明,栗疫病菌(Cryphonectria parasitica)的两个dicer基因之一dcl-2的破坏会增加对真菌病毒感染的易感性(G.C. 塞格斯、张X、邓F、孙Q和D.L. 努斯,《美国国家科学院院刊》104:12902 - 12906,2007年)。我们现在报告,在感染低毒病毒CHV1-EP713的野生型和dicer基因dcl-1突变型寄生隐孢壳菌株中积累了病毒衍生的小RNA(vsRNAs),但在感染低毒病毒的dcl-2突变型和dcl-1 dcl-2双突变型菌株中未积累。CHV1-EP713 vsRNAs由病毒正链和负链RNA产生,比例为3:2,沿病毒基因组呈非随机分布。我们还表明,寄生隐孢壳菌对低毒病毒和真菌呼肠孤病毒感染的反应是dcl-2表达显著增加(12至20倍),而dcl-1的表达仅适度增加(2倍)。在用缺乏RNA沉默p29抑制因子的低毒病毒CHV1-EP713突变体感染后,dcl-2的表达进一步增加(约35倍)。综合结果证明了真菌宿主中通过特定dicer基因dcl-2的作用产生真菌病毒衍生的小RNA。它们还揭示,dcl-2表达在对真菌病毒感染的反应中被显著诱导,其机制似乎被低毒病毒编码的RNA沉默p29抑制因子所抑制。

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Curr Protoc Microbiol. 2006 Jan;Chapter 16:Unit 16H.2. doi: 10.1002/9780471729259.mc16h02s00.
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