Monden Yuki, Takasaki Kazuto, Futo Satoshi, Niwa Kousuke, Kawase Mitsuo, Akitake Hiroto, Tahara Makoto
Graduate School of Environmental and Life Science, Okayama University, 1-1-1 Tsushimanaka Kitaku, Okayama, Okayama 700-8530, Japan.
FASMAC Co., Ltd., 5-1-3 Midorigaoka, Atsugi, Kanagawa 243-0041, Japan.
J Biotechnol. 2014 Sep 20;185:57-62. doi: 10.1016/j.jbiotec.2014.06.013. Epub 2014 Jun 19.
In many crops species, the development of a rapid and precise cultivar discrimination system has been required for plant breeding and patent protection of plant cultivars and agricultural products. Here, we successfully evaluated strawberry cultivars via a novel method, namely, the single tag hybridization (STH) chromatographic printed array strip (PAS) using the PCR products of eight genomic regions. In a previous study, we showed that genotyping of eight genomic regions derived from FaRE1 retrotransposon insertion site enabled to discriminate 32 strawberry cultivars precisely, however, this method required agarose/acrylamide gel electrophoresis, thus has the difficulty for practical application. In contrast, novel DNA detection method in this study has some great advantages over standard DNA detection methods, including agarose/acrylamide gel electrophoresis, because it produces signals for DNA detection with dramatically higher sensitivity in a shorter time without any preparation or staining of a gel. Moreover, this method enables the visualization of multiplex signals simultaneously in a single reaction using several independent amplification products. We expect that this novel method will become a rapid and convenient cultivar screening assay for practical purposes, and will be widely applied to various situations, including laboratory research, and on-site inspection of plant cultivars and agricultural products.
在许多作物品种中,植物育种以及植物品种和农产品的专利保护都需要快速精确的品种鉴别系统。在此,我们通过一种新方法成功评估了草莓品种,即使用八个基因组区域的PCR产物进行单标签杂交(STH)色谱打印阵列条带(PAS)分析。在先前的一项研究中,我们表明源自FaRE1反转录转座子插入位点的八个基因组区域的基因分型能够精确区分32个草莓品种,然而,该方法需要琼脂糖/丙烯酰胺凝胶电泳,因此在实际应用中存在困难。相比之下,本研究中的新型DNA检测方法相对于包括琼脂糖/丙烯酰胺凝胶电泳在内的标准DNA检测方法具有一些显著优势,因为它在更短的时间内以更高的灵敏度产生DNA检测信号,无需对凝胶进行任何制备或染色。此外,该方法能够在单个反应中使用几种独立的扩增产物同时可视化多重信号。我们期望这种新方法将成为一种用于实际目的的快速便捷的品种筛选分析方法,并将广泛应用于各种情况,包括实验室研究以及植物品种和农产品的现场检测。