Lin Ling, Wang Xiping, Wang Yuejin
Key Laboratory of Northwest Horticulture Plant Germplasm and Genetic Improvement of Ministry of Agriculture of People's Republic of China.
Mol Biol Rep. 2006 Sep;33(3):197-206. doi: 10.1007/s11033-006-0008-5.
Powdery mildew, caused by Uncinula necator Burr, is one of the most seriously damaging diseases of grapevine all over the world. To gain the novel gene and investigate the resistance mechanism in Chinese Wild Vitis pseudoreticulata clone Baihe-35-1, mRNA differential display was employed to study the differential expression of the resistant gene to the disease of it when inoculated by Uncinula necator under natural field conditions, 5' RACE and 3' RACE have been used to clone the whole cDNA sequences of VpAPX, the novel gene related to Ascorbate Peroxidase which involved in resistant to the disease, is composed of specific sequence 1077 bp and has an open reading frame of 750 bp coding for 250 amino acid residues with a molecular weight of 27.566 kDa. The VpAPX gene was obtained by polymerase chain reaction (PCR) with the special primers synthesized according to the sequences of cDNA, and further cloned it into the pGEM-T easy vector. The cloned VpAPX gene was cut out again with two restriction enzymes and was inserted into the prokaryotic expression vector pGEX-4T-1, then transferred into E. coli BL21. As result, GST-VpAPX fusion protein was successfully expressed by induction of IPTG and purified by GST affinity resin. After injecting rabbit, the polyclonal antibodies were produced. Western blot analyses showed that the antibody reacted specifically to GST-VpAPX fusion protein and the titer for this antibody is 10(5). This research made the foundation to transform the VpAPX gene into grape plants for follow research in processing.
由葡萄钩丝壳菌(Uncinula necator Burr)引起的白粉病是全球葡萄最具严重危害的病害之一。为获得新基因并研究中国野生葡萄白河 -35-1 的抗病机制,采用 mRNA 差异显示技术研究其在自然田间条件下接种葡萄钩丝壳菌后抗病基因的差异表达,利用 5' RACE 和 3' RACE 克隆了抗坏血酸过氧化物酶相关新基因 VpAPX 的全长 cDNA 序列,该基因由 1077 bp 的特异序列组成,有一个 750 bp 的开放阅读框,编码 250 个氨基酸残基,分子量为 27.566 kDa。根据 cDNA 序列合成特异引物,通过聚合酶链反应(PCR)获得 VpAPX 基因,并进一步克隆到 pGEM-T easy 载体中。用两种限制性内切酶再次切出克隆的 VpAPX 基因,插入原核表达载体 pGEX-4T-1,然后转入大肠杆菌 BL21。结果,经 IPTG 诱导成功表达 GST-VpAPX 融合蛋白,并通过 GST 亲和树脂纯化。注射兔子后产生了多克隆抗体。蛋白质免疫印迹分析表明该抗体与 GST-VpAPX 融合蛋白特异性反应,抗体效价为 10⁵。本研究为将 VpAPX 基因转化到葡萄植株中进行后续研究奠定了基础。