The Guangdong Subcenter of National Center for Soybean Improvement, State Key Laboratory of Agricultural and Biological Resources Protection and Utilization in Subtropics, College of Agriculture, South China Agricultural University, Guangzhou, Guangdong, P. R. China.
PLoS One. 2012;7(9):e45568. doi: 10.1371/journal.pone.0045568. Epub 2012 Sep 18.
Gibberellic acids (GAs) are plant hormones that play fundamental roles in plant growth and developmental processes. Previous studies have demonstrated that three key enzymes of GA20ox, GA3ox, and GA2ox are involved in GA biosynthesis. In this study, the Arabidopsis DREB1A gene driven by the CaMV 35S promoter was introduced into soybean plants by Agrobacterium- mediated transformation. The results showed that the transgenic soybean plants exhibited a typical phenotype of GA-deficient mutants, such as severe dwarfism, small and dark-green leaves, and late flowering compared to those of the non-transgenic plants. The dwarfism phenotype was rescued by the application of exogenous GA(3) once a week for three weeks with the concentrations of 144 µM or three times in one week with the concentrations of 60 µM. Quantitative RT-PCR analysis revealed that the transcription levels of the GA synthase genes were higher in the transgenic soybean plants than those in controls, whereas GA-deactivated genes except GmGA2ox4 showed lower levels of expression. The transcript level of GmGA2ox4 encoding the only deactivation enzyme using C(20)-GAs as the substrates in soybean was dramatically enhanced in transgenic plants compared to that of wide type. Furthermore, the contents of endogenous bioactive GAs were significantly decreased in transgenic plants than those of wide type. The results suggested that AtDREB1A could cause dwarfism mediated by GA biosynthesis pathway in soybean.
赤霉素(GAs)是植物激素,在植物生长和发育过程中起着至关重要的作用。先前的研究表明,GA20ox、GA3ox 和 GA2ox 这三个关键酶参与了 GA 的生物合成。在这项研究中,通过农杆菌介导的转化将 CaMV 35S 启动子驱动的拟南芥 DREB1A 基因导入大豆植株中。结果表明,与非转基因植株相比,转基因大豆植株表现出典型的 GA 缺陷型突变体表型,如严重矮化、叶片小而深绿、开花晚。每周一次应用外源 GA(3)(浓度为 144 µM)连续三周或每周三次应用浓度为 60 µM 可以挽救矮化表型。定量 RT-PCR 分析显示,转基因大豆植株中 GA 合酶基因的转录水平高于对照,而除 GmGA2ox4 外的 GA 失活基因的表达水平较低。编码大豆中唯一以 C(20)-GAs 为底物的失活酶的 GmGA2ox4 的转录水平在转基因植株中显著高于野生型。此外,转基因植株中内源生物活性 GA 的含量明显低于野生型。结果表明,AtDREB1A 可以通过 GA 生物合成途径引起大豆的矮化。