Liu Gui-Feng, Cheng Gui-Lan, Jiang Jing, Bai Shuang, Yu Ying, Cai Zhi-Jun, Dong Jing-Xiang, Li Shu-Juan
Heilongjiang Provincial Key Laboratory of Teaching and Research Section of Forestry Genetics and Breeding, Northeast Forestry University, Harbin 150040, China.
Zhi Wu Sheng Li Yu Fen Zi Sheng Wu Xue Xue Bao. 2006 Apr;32(2):163-8.
In this study, betA gene was introduced into the pollen plantlets of Populus simonii x P. nigra using Agrobacterium-mediated transformation. The four kanamycine-resistant plants obtained were identified as transgenic plants by PCR detection and the results were all positive. The result of quantitative real-time PCR detection showed that the betA gene was transcribed and expressed in all the transformed plants, but the transcript levels are different. Test of salt-tolerance of the transgenic plants showed that 80%-00% of transgenic plants were rooted while 0 of non-transgenic plants were rooted at 0.55% NaCl stress, and 0 of transgenic plants were rooted at 0.70%-0.80% NaCl stress. The betaine content analysis showed the betaine content of the transgenic plants are obviously higher than that in non-transgenic plants, so transformation betA gene raised the salt tolerance to the transgenic plants.
本研究采用农杆菌介导的转化方法,将betA基因导入小叶杨×黑杨的花粉植株中。通过PCR检测,获得的4株卡那霉素抗性植株被鉴定为转基因植株,结果均为阳性。实时定量PCR检测结果表明,betA基因在所有转化植株中均转录表达,但转录水平不同。转基因植株的耐盐性试验表明,在0.55% NaCl胁迫下,80%-100%的转基因植株生根,而非转基因植株无生根;在0.70%-0.80% NaCl胁迫下,有部分转基因植株生根。甜菜碱含量分析表明,转基因植株的甜菜碱含量明显高于非转基因植株,因此转入betA基因提高了转基因植株的耐盐性。