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作 者:陈国华[1] 肖罗[2] 张双庆[3] 杨宇红[1] 谢丙炎[1]
机构地区:[1]中国农业科学院蔬菜花卉研究所,北京100081 [2]湖南农业大学,长沙410007 [3]美国密西西比大学药学院,密西西比38677
出 处:《植物病理学报》2008年第5期509-513,共5页Acta Phytopathologica Sinica
基 金:国家自然科学基金资助项目(30571261;30270236);"十一五"国家高技术研究发展计划课题(2006AA10Z1119);重大基础研究前期研究专项(2004CCA05300);农业公益性行业科研专项经费项目(nyzx07-050)
摘 要:促分裂原活化蛋白激酶(mitogen-activated protein kinase,MAPK)在线虫的生长发育等方面具有重要作用,本研究探索利用RNAi技术沉默南方根结线虫mapk-1基因来抑制线虫的生长发育。根据mapk-1基因的cDNA序列设计引物,通过体外转录合成约550bp的dsRNA对南方根结线虫的卵进行RNAi以沉默mapk-1基因。试验结果表明,将南方根结线虫的卵块浸泡在含有2mg/mL dsRNA的M9缓冲溶液中,24h后卵块孵化出的2龄幼虫数量明显多于对照组(无dsRNA),但孵化出的幼虫死亡率高达90%,而对照组的死亡率低于5%,说明mapk-1基因的沉默抑制了卵块的孵化和线虫的生长,同时将孵化的幼虫接种番茄,14d后番茄根部无根结产生,35d后无卵块产生;而浸泡72h后卵块孵化出的2龄幼虫几乎全部死亡,并且孵化的线虫数量明显少于对照。提取导入dsRNA的卵块的RNA进行半定量PCR分析,结果表明mapk-1基因的mRNA被降解。Mitogen-activated protein kinase(MAPK)plays an important role in development of nematode.By using RNA interference technique,controlling was studied the expression of mapk-1.Primers were designed based on the cDNA sequence of mapk-1 and a dsRNA about 550 bp was synthesized by vitro transcription to soak the egg masses of Meloidogyne incognita.The results showed that the amount of J2 in egg masses treated with 2 mg/mL dsRNA for 24 hours was significantly greater than that in control group,but the mortality rate in treated group was reached 90%,however,the value in control group was not more than 5%.In addition,the tomato roots had no knot at 14 days postinfection(dpi)and no egg mass at 35 dpi when inoculated the J2.When egg masses were soaked in 2 mg/mL dsRNA for 72 hours,the morality rate of J2 was almost 100% and the amount of J2 was markedly less than control group.RT-PCR analysis showed lower transcript abundance for the targeted mRNAs than control.
关 键 词:南方根结线虫 卵块 促分裂原活化蛋白激酶(MAPK) RNAI
分 类 号:S432.45[农业科学—植物病理学]
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