利用西葫芦黄花叶病毒工程技术建立一种简便快速的西葫芦基因传递系统

Mi-Hyung Kang, Jang-Kyun Seo, Hoseong Choi, Hongsoo Choi, Kook Hyung Kim
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引用次数: 10

摘要

从南瓜中分离得到西葫芦黄花叶病毒(ZYMV)分离物PA (pZYMV-PA),利用病毒转录和加工信号,构建了具有传染性的西葫芦黄花叶病毒(ZYMV)体内转录物全长cDNA克隆。pZYMV-PA质粒dna的简单摩擦接种成功地引起西葫芦(Cucurbita pepo L.)植株的侵染。我们进一步设计了这个传染性的ZYMV cDNA克隆作为异源蛋白在葫芦中的系统表达的病毒载体。我们通过简单地摩擦接种基于zymv表达构建的质粒dna,成功地在西葫芦植物中表达了gfp和bar两个报告基因。我们建立的基于zymv的病毒载体与简单的摩擦接种相结合的方法,为葫芦中外源基因的导入和评价提供了一种简便、快速的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Establishment of a Simple and Rapid Gene Delivery System for Cucurbits by Using Engineered of Zucchini yellow mosaic virus
The infectious full-length cDNA clone of zucchini yellow mosaic virus (ZYMV) isolate PA (pZYMV-PA), which was isolated from pumpkin, was constructed by utilizing viral transcription and processing signals to produce infectious in vivo transcripts. Simple rub-inoculation of plasmid DNAs of pZYMV-PA was successful to cause infection of zucchini plants (Cucurbita pepo L.). We further engineered this infectious cDNA clone of ZYMV as a viral vector for systemic expression of heterologous proteins in cucurbits. We successfully expressed two reporter genes including gfp and bar in zucchini plants by simple rub-inoculation of plasmid DNAs of the ZYMV-based expression constructs. Our method of the ZYMV-based viral vector in association with the simple rub-inoculation provides an easy and rapid approach for introduction and evaluation of heterologous genes in cucurbits.
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