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C4和βC1在介导转录后基因沉默抑制中的不同作用:来自单组分双生病毒——黄秋葵黄脉花叶病毒C2反式激活的证据

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.

作者信息

Gopal P, Pravin Kumar P, Sinilal B, Jose J, Kasin Yadunandam A, Usha R

机构信息

Department of Plant Biotechnology, School of Biotechnology, Madurai Kamaraj University, Madurai, Tamil Nadu 625021, India.

出版信息

Virus Res. 2007 Jan;123(1):9-18. doi: 10.1016/j.virusres.2006.07.014. Epub 2006 Sep 1.

Abstract

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 silencing activities 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.

摘要

黄秋葵黄脉花叶病(BYVMD)由一种DNAβ卫星与双生病毒组分共同引起。双生病毒组分有两个启动子,一个在病毒链(V链)上,另一个在基因间隔区(IR)的互补链(C链)上。为了研究V链和C链启动子的启动子活性,在启动子下游构建了mGFP基因融合体。在本氏烟草叶片中的瞬时和稳定表达显示,在C链启动子下有显著的绿色荧光蛋白(GFP)表达,而在没有反式激活因子C2的情况下,V链启动子下的表达非常弱。用含有单独的V链-GFP或与C1、C2、C4、V1、V2或βC1(正反义方向)的二元载体构建体对未转化的本氏烟草植株进行农杆菌浸润,以了解这些基因产物在反式激活和/或抑制转录后基因沉默(PTGS)中的作用。结果表明,C4和βC1对基因沉默活性有强烈抑制作用,而C2的抑制作用较弱。通过农杆菌浸润和接种,在gfp沉默的GFP16c/GFPi植株中也证实了这种抑制活性。与上述其他病毒基因相比,作为转基因的C4和βC1的表达产生了异常的表型生长,进一步支持了它们的抑制功能。

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