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国家自然科学基金(30370979)

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农杆菌介导法获得转pac1基因小麦并表现对大麦黄矮病毒的抗性被引量:14
2006年
自裂殖酵母中克隆得到pac1基因,与GenBank中相关的核苷酸序列有99.3%的相似性.编码蛋白质序列分析表明,其具有RNaseⅢ结构域和双链RNA结合结构域.体外活性测定表明,以pET.5a系统在大肠杆菌中表达的pac1产物能够降解dsRNA.将pac1导入双元载体pBll21,以培养7~10d的小麦幼胚为受体材料,利用农杆菌株LBA4404对小麦品种陇鉴127进行转化,获得了41株G418抗性植株,经点杂交(dot blot)、RT-PCR和nptⅡ ELISA检测证实,其中25株整合有外源基因并能正常表达.对这25株转基因小麦进行大麦黄矮病毒的抗性鉴定表明,有12株表现低度抗性,表现为低接毒量时无症状,接毒量提高时发病且严重;有12株表现中度抗性,表现为低接毒量时无症状,接毒量提高时局部有不严重症状;有1株表现高度抗性,两种情况下均无症状.抗性实验结果表明了pac1介导的抗性具有剂量效应的特点。
燕飞郑银英张文蔚肖红李世访成卓敏
关键词:农杆菌介导法小麦转基因抗病毒大麦黄矮病毒
Obtained transgenic wheat expressing pac1 mediated by Agrobacterium is resistant against Barley yellow dwarf virus-GPV被引量:5
2006年
In fission yeast (Schizosaccharomyces pombe), pac1 gene was cloned with 99.3% nucleo- tide sequence similarity with published pac1 in GenBank. In pET-5α expression system, the expres- sion product of cloned pac1 in E. coli showed activity to degrade the double-strand RNA. Harboring the binary vector pBI121, which contains pac1 gene, Agrobacterium tumefaciens strain LBA4404 was used to transform the wheat immature embryos pre- cultured 7―10 d. After preregeneration, regeneration and selection culture stage, totally 41 G418 resistant plants were obtained, in which 25 lines were proved to integrate with transgene and express transgene normally by PCR, Dot blot, RT-PCR and ELISA de- tection. Antivirus test carried out on 25 positive lines with high dose of Barley yellow dwarf virus-GPV re- vealed that 12 lines had resistance to BVDV-GPV in low level, another 12 lines had resistance to BVDV- GPV in middle level, and 1 line showed resistance to BVDV-GPV in high level. However, both low and middle level of resistance plants showed no symp- toms when infected by viruses at low dose, which suggested the dose-dependent effect of the resis- tance mediated by pac1 to BYDV-GPV.
YAN Fei ZHENG Yinying ZHANG Wenwei XIAO Hong LI Shifang CHENG Zhuomin
关键词:转基因小麦土壤杆菌大麦黄矮病
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