以低温处理的水稻辽盐241植株叶片总RNA为模板, 用OsMAPK4基因特异引物通过RT-PCR扩增出OsMAPK4基因, 构建了由E12启动子调控的OsMAPK4基因植物表达载体pBME12。通过农杆菌介导法将OsMAPK4基因导入烟草, 筛选获得25株转基因植株。抗旱性研究结果表明, OsMAPK4基因的超量表达提高了T1代转基因植株的抗旱性。卡那霉素抗性在T1代转基因植株中的分离情况表明, 大多数转基因株系符合单基因遗传规律。

OsMAPK4 gene was obtained by RT-PCR using gene special primer from Liaoyan241 leaf treated with low temperature. Plant expression vector pBME12 was constructed in which OsMAPK4 gene was regulated by E12 promoter. OsMAPK4 gene was transferred into tobacco via Agrobacterium-mediated method and 25 transgenic plants obtained. The results of drought resistance experiments showed that overexpression of OsMAPK4 gene conferred enhanced drought resistance of T1 transgenic plants. Kanamycin-resistance segregation in T1 transgenic plants showed that the most transgenic lines were in single gene inheritance.