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首页> 外文期刊>Virus Research: An International Journal of Molecular and Cellular Virology >Differential roles of C4 and betaC1 in mediating suppression of post-transcriptional gene silencing: evidence for transactivation by the C2 of Bhendi yellow vein mosaic virus, a monopartite begomovirus.
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Differential roles of C4 and betaC1 in mediating suppression of post-transcriptional gene silencing: evidence for transactivation by the C2 of Bhendi yellow vein mosaic virus, a monopartite begomovirus.

机译:C4和betaC1在介导转录后基因沉默抑制中的不同作用:单倍体begomovirus Bhendi黄脉花叶病毒C2的反式激活证据。

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摘要

Bhendi yellow vein mosaic disease (BYVMD) is caused by the association of a DNA beta satellite with a begomovirus component. The begomovirus component has two promoters, one in the virion sense (V-sense) and the other in the complementary sense (C-sense) in the intergenic region (IR). To study the promoter activities of V-sense and C-sense promoters, mGFP gene fusion was made downstream to the promoters. Transient and stable expressions in N. benthamiana leaves showed significant GFP expression under C-sense promoter whereas the expression under the V-sense promoter was very weak in the absence of the transactivator C2. Untransformed N. benthamiana plants were agroinfiltrated with binary vector constructs containing V-sense-GFP alone or along with C1, C2, C4, V1, V2 or betaC1 (in both sense and antisense orientations) to understand the roles of these gene products in transactivation and/or suppression of post-transcriptional gene silencing (PTGS). The results showed strong suppression of gene silencingactivities for C4 and betaC1 but a weak activity for C2. The suppression activities were also confirmed using gfp-silenced GFP16c/GFPi plants by agroinfiltration and agroinoculation. The expression of C4 and betaC1 as transgenes produced abnormal phenotypic growth compared to the other viral genes mentioned above, further supporting their suppressor function.
机译:Bhendi黄脉花叶病(BYVMD)是由DNA beta卫星与begomovirus成分的关联引起的。该begomovirus组件在基因间区域(IR)中具有两个启动子,一个在病毒体意义上(V-sense),另一个在互补意义上(C-sense)。为了研究V-正义和C-正义启动子的启动子,在启动子的下游进行了mGFP基因融合。本生烟草叶片中的瞬时和稳定表达在C感官启动子下显示出显着的GFP表达,而在没有反式激活因子C2的情况下V感官启动子下的表达非常弱。用仅包含V-sense-GFP或连同C1,C2,C4,V1,V2或betaC1(有义和反义方向)的二元载体构建体对未转化的本氏烟草植物进行农杆菌浸润,以了解这些基因产物在反式激活中的作用和/或抑制转录后基因沉默(PTGS)。结果表明,C4和betaC1的基因沉默活性受到强烈抑制,而C2的活性却弱。通过农杆菌浸润和农杆菌接种,使用gfp沉默的GFP16c / GFPi植物也证实了抑制活性。与上述其他病毒基因相比,C4和betaC1作为转基因的表达产生异常的表型生长,进一步支持了它们的抑制功能。

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