Hernandez-Garcia Carlos M, Martinelli Adriana P, Bouchard Robert A, Finer John J
Department of Horticulture and Crop Science, OARDC/The Ohio State University, Wooster, OH 44691, USA.
Plant Cell Rep. 2009 May;28(5):837-49. doi: 10.1007/s00299-009-0681-7. Epub 2009 Feb 20.
The success of plant genetic transformation relies greatly on the strength and specificity of the promoters used to drive genes of interest. In this study, we analyzed gfp gene expression mediated by a polyubiquitin promoter (Gmubi) from soybean (Glycine max) in stably transformed soybean tissues. Strong GFP expression was observed in stably transformed proliferative embryogenic tissues. In whole transgenic plants, GFP expression was observed in root tips, main and lateral roots, cotyledons and plumules in young plants as well as in leaf veins, petioles, flower petals, pollen, pods and developing seeds in mature plants. GFP expression was localized mainly in epidermal cells, leaf mesophyll, procambium and vascular tissues. Introduction of an intron-less version of the Gmubi promoter (Gmupri) displayed almost the same GFP expression pattern albeit at lower intensities. The Gmubi promoter showed high levels of constitutive expression and represents an alternative to viral promoters for driving gene expression in soybean.
植物遗传转化的成功很大程度上依赖于用于驱动目的基因的启动子的强度和特异性。在本研究中,我们分析了来自大豆(Glycine max)的多聚泛素启动子(Gmubi)介导的绿色荧光蛋白(gfp)基因在稳定转化的大豆组织中的表达。在稳定转化的增殖胚性组织中观察到强烈的绿色荧光蛋白表达。在整个转基因植株中,在幼嫩植株的根尖、主根和侧根、子叶和胚芽中以及在成熟植株的叶脉、叶柄、花瓣、花粉、豆荚和发育中的种子中均观察到绿色荧光蛋白表达。绿色荧光蛋白表达主要定位于表皮细胞、叶肉、原形成层和维管组织。引入无内含子版本的Gmubi启动子(Gmupri)显示出几乎相同的绿色荧光蛋白表达模式,尽管强度较低。Gmubi启动子表现出高水平的组成型表达,是在大豆中驱动基因表达的病毒启动子的一种替代选择。