EV71 3D(pol)转录活性域的鉴定

Xiao Xu, Yunfang Yao, Jing Li, Keli Chai, Wentao Qiao, Juan Tan
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引用次数: 0

摘要

肠病毒71型(EV71)是手足口病的主要病原体之一。EV71基因组编码RNA依赖性RNA聚合酶(RdRp) 3D(pol),该酶对基因组转录和翻译至关重要。然而,3D(pol)如何与宿主相互作用仍不清楚。酵母双杂交系统为检测蛋白质相互作用提供了一种有效的方法。本文将3D(pol)的DNA序列插入pGBKT7载体中,作为酵母双杂交实验的诱饵质粒,并将质粒转化为酵母AH109菌株。我们检测了3D(pol)的表达、细胞毒性和自身活性。3D(pol)表达良好,不影响细胞生长,但在酵母细胞中表现出强烈的转录激活。我们进一步构建了一系列pGBKT7-3D(pol)缺失突变体,并使用自激活实验确定了最短的转录激活域(1-94aa)。该结果为利用酵母双杂交系统筛选与3D(pol)相互作用的宿主蛋白提供了分子基础。
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[Identification of the Transcriptional Activity Domain of EV71 3D(pol)].

Enterovirus 71(EV71)is one of the major pathogens of hand, foot and mouth disease (HFMD). The EV71 genome encodes an RNA-dependent RNA polymerase(RdRp),3D(pol),which is critical for genome transcription and translation. However, how the 3D(pol) interacts with the host remains unclear. Yeast two-hybrid systems provide an effective approach for detecting protein-protein interactions. In this report, we inserted the DNA sequence of 3D(pol) into the pGBKT7 vector as the bait plasmid for the yeast two-hybrid experiment and transformed the plasmid into the yeast AH109 strain. We detected the expression,cytotoxicity and self-activity of 3D(pol).The 3D(pol) expressed well without affecting cell growth but exhibited strong transcriptional activation in yeast cells. We further constructed a series of pGBKT7-3D(pol) deletion mutants and identified the shortest transcriptional activation domain(1-94aa)using a self-activation assay. The results provide a molecular basis for screening the host proteins that interact with 3D(pol) using the yeast two hybrid system.

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