Krubphachaya Pongrit, Jurícek Míla, Kertbundit Sunee
Institute of Molecular Biology and Genetics, Mahidol University, Nakon Pathom, Thailand.
J Biochem Mol Biol. 2007 May 31;40(3):404-11. doi: 10.5483/bmbrep.2007.40.3.404.
Transformation of cantaloupes with the coat protein (cp) gene of papaya ringspot virus type W (PRSV-W), Thai isolate, was used to introduce virus resistance. Binary vectors containing either the full length coat protein coding region under control of the 35S CaMV promoter(pSA1175), or the inverted-repeat of a coat protein coding region (pSA1304), were constructed and used for Agrobacterium-mediated transformation of cotyledonary explants of the cantaloupe cultivar Sun Lady. Four independent transgenic lines were obtained using pSA1304 and one using pSA1175. Integration of the PRSV-W cp gene into the genome of these transgenic lines was verified by PCR amplification, GUS assays and Southern blot hybridization. In vitro inoculation of these lines with PRSV-W revealed that whereas the line containing pSA1175 remained sensitive, the four lines containing pSA1304 were resistant. The presence of small RNA species, presumably siRNA, corresponding to regions of the viral cp gene in transgenic lines resistant to PRSV-W supports the involvement of post-transcriptional gene silencing in the establishment of resistance.
利用木瓜环斑病毒W型(PRSV-W)泰国分离株的外壳蛋白(cp)基因转化甜瓜以引入病毒抗性。构建了含有在35S CaMV启动子控制下的全长外壳蛋白编码区的双元载体(pSA1175),或外壳蛋白编码区的反向重复序列的双元载体(pSA1304),并用于农杆菌介导的甜瓜品种“太阳女士”子叶外植体的转化。使用pSA1304获得了4个独立的转基因株系,使用pSA1175获得了1个转基因株系。通过PCR扩增、GUS检测和Southern杂交验证了PRSV-W cp基因整合到这些转基因株系的基因组中。用PRSV-W对这些株系进行体外接种,结果显示含有pSA1175的株系仍然敏感,而含有pSA1304的4个株系具有抗性。在对PRSV-W具有抗性的转基因株系中,存在与病毒cp基因区域相对应的小RNA种类,推测为siRNA,这支持转录后基因沉默参与了抗性的建立。