Kang Minji, Seo Jang-Kyun, Choi Hoseong, Choi Hong-Soo, Kim Kook-Hyung
Department of Agricultural Biotechnology and Research Institute of Agriculture and Life Sciences, Seoul National University, Seoul 151-921, Korea.
Crop Protection Division, National Academy of Agricultural Science, Wanju 565-852, Korea.
Plant Pathol J. 2016 Feb;32(1):70-6. doi: 10.5423/PPJ.NT.08.2015.0173. Epub 2016 Feb 1.
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.
从南瓜中分离得到的西葫芦黄花叶病毒(ZYMV)分离株PA的感染性全长cDNA克隆(pZYMV-PA),是利用病毒转录和加工信号构建而成,用于在体内产生感染性转录本。通过简单的摩擦接种pZYMV-PA的质粒DNA成功感染了西葫芦植株(西葫芦)。我们进一步将这种ZYMV感染性cDNA克隆改造成一种病毒载体,用于在葫芦科植物中全身表达异源蛋白。通过简单摩擦接种基于ZYMV的表达构建体的质粒DNA,我们在西葫芦植株中成功表达了包括gfp和bar在内的两个报告基因。我们基于ZYMV的病毒载体方法与简单摩擦接种相结合,为在葫芦科植物中引入和评估异源基因提供了一种简便快捷的方法。