Chen Shih-Cheng, Liu Hui-Wen, Lee Kung-Ta, Yamakawa Takashi
Graduate Institute of Microbiology and Biochemistry, National Taiwan University, 1, Sec. 4, Roosevelt Road, Taipei, Taiwan.
Plant Cell Rep. 2007 Jan;26(1):29-37. doi: 10.1007/s00299-006-0175-9. Epub 2006 Jul 28.
The chimerical gene, Arabidopsis thaliana sHSP18.2 promoter fused to E. coli gusA gene, was Agrobacterium rhizogenes-mediated transformed into Nicotiana tabacum as a heat-regulatable model, and the thermo-inducible expression of GUS activity in N. tabacum transgenic hairy roots was profiled. An activation of A. rhizogenes with acetosyringone (AS) before cocultured with tobacco's leaf disc strongly promoted transgenic hairy roots formation. Transgenic hairy roots formation efficiency of A. rhizogenes precultured with 200 microM AS supplementation was 3.1-fold and 7.5-fold, respectively, compared to the formation efficiency obtained with and without AS supplementation in coculture. Transgenic hairy roots transformed with different AS concentration exhibited a similar pattern of thermo-inducibility after 10 min to 3 h heat treatments detected by GUS expression. The peak of expressed GUS specific activity, 399,530 pmol MUG per mg total protein per min, of the transgenic hairy roots was observed at 48 h after 3 h of 42 degrees C heat treatment, and the expressed GUS specific activity was 7-26 times more than that reported in A. thaliana, tobacco BY-2 cells and Nicotiana plumbaginifolia. Interference caused by AS supplementation on the growth of transgenic hairy roots, time-course of GUS expression and its expression level were not observed.
将拟南芥小热激蛋白18.2启动子与大肠杆菌gusA基因融合而成的嵌合基因,通过发根农杆菌介导转化到烟草中作为热调控模型,并对烟草转基因毛状根中GUS活性的热诱导表达进行了分析。在用乙酰丁香酮(AS)激活发根农杆菌后与烟草叶盘共培养,强烈促进了转基因毛状根的形成。与共培养中添加和不添加AS时获得的形成效率相比,用200微摩尔AS补充预培养的发根农杆菌的转基因毛状根形成效率分别提高了3.1倍和7.5倍。通过GUS表达检测,在10分钟至3小时的热处理后,用不同AS浓度转化的转基因毛状根表现出相似的热诱导模式。在42℃热处理3小时后48小时观察到转基因毛状根的GUS比活性峰值为每分钟每毫克总蛋白399,530皮摩尔MUG,且表达的GUS比活性比拟南芥、烟草BY-2细胞和垂序烟草中报道的高7至26倍。未观察到AS补充对转基因毛状根生长、GUS表达的时间进程及其表达水平的干扰。