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作 者:郭兆奎[1] 杨谦[1] 姚泉洪[2] 万秀清 颜培强
机构地区:[1]哈尔滨工业大学生命科学与工程系,哈尔滨150001 [2]上海市农业科学院生物技术研究所,上海市农业遗传育种重点实验室,上海201106 [3]黑龙江省烟草科学研究所,牡丹江157011
出 处:《高技术通讯》2007年第11期1174-1179,共6页Chinese High Technology Letters
基 金:国家烟草专卖局科技攻关项目(110200101008)资助.
摘 要:提取拟南芥总RNA,反转录合成Na+/H+逆向转运蛋白基因AtNHX1,构建了植物高效表达载体,用叶盘法将其导入烟草,经筛选获得了抗卡那霉素和GUS染色阳性的转化子38株。应用荧光定量PCR方法对转化材料部分含AtNHX1基因的烟草内源钾通道基因、烟草K+转运蛋白基因和烟草焦磷酸酶基因的转录水平进行了分析。结果表明:在转化烟草中可以检测到AtNHX1基因mRNA,与未转化材料相比,烟草钾离子转运蛋白基因NtHAK1的转录降低,H+-ATPase基因NHA1转录增加,钾通道基因NKT转录无显著变化,T1代转化烟叶中K+含量显著增加,Na^+、Ca^2+无显著变化,烟叶中总糖含量降低,证明了编码拟南芥AtNHX1基因与植物的K+吸收有关。The vacuolar Na^+/H^+ antiporter gene AtNHX1 was cloned from Arabidopsis thaliana using RNA isolation and RTPCR methods. The binary vector containing AtNHX1 gene was constructed, and introduced into tobacco via Agrobacterium-mediated leaf disk transformation. Thirty-eight transgenic tobacco plants which appeared kanamycin resistance and GUS assay positive were obtained by AtNHX1 PCR screening. Transcript levels of AtNHX1 and four tobacco genes in- volved in K^+ uptake, including NKT (K^+ channel), NtHAK1 (K^+ transporter), NHA1 (P-H^+ -ATPase) and PPA (V- H^+ -PPase) in the AtNHX1 modified tobacco roots were analyzed by real-time PCR. The mRNA of AtNHX1 can be detected in the transgenic plants. The transcript of P-H ^+ -ATPase gene NHA 1 is up-regulation, and that of potassium transporter gene NtHAK1 is down-regulation. No significant alteration can be found in the transcript of potassium channel NKT1. The potassium content in the leaves of AtNHX1 transgenic tobacco T1 generation is increased by about 53.9% and the sugar content is significantly reduced, however, no significant changes was found in Na^+and Ca^2+contents in tobacco leaves. Our data indicate that AtNHX1 plays an important role in potassium uptake.
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