Department of Biotechnology and Kumho Life Science Laboratory, Chonnam National University, Gwangju, 500-757, Korea.
Plant Cell Rep. 2015 Feb;34(2):265-75. doi: 10.1007/s00299-014-1705-5. Epub 2014 Nov 20.
A plant-derived 0.3 kb constitutive promoter was obtained from AtTCTP expression analysis, and successfully applied to the expression of a selectable marker gene for production of transgenic creeping bentgrass plants. The isolation and use of an efficient promoter is essential to develop a vector system for efficient genetic transformation of plants, and constitutive promoters are particularly useful for the expression of selectable marker genes. In this study, we characterized a small size of the constitutive promoter from the expression analysis of Arabidopsis thaliana translationally controlled tumor protein (AtTCTP) gene. Histochemical and fluorometric GUS analyses revealed that a 303 bp upstream region from the start codon of the AtTCTP gene showed strong GUS expression throughout all plant tissues, which is approximately 55 % GUS activity compared with the cauliflower mosaic virus 35S promoter (35Spro). To examine the possible application of this promoter for the development of genetically engineered crops, we introduced pCAMBIA3301 vector harboring the 0.3 kb promoter of AtTCTP (0.3kbpro) that was fused to the herbicide resistance BAR gene (0.3kb pro ::BAR) into creeping bentgrass. Our transformation results demonstrate that transgenic creeping bentgrass plants with herbicide resistance were successfully produced using 0.3kb pro ::BAR as a selectable marker. Northern blot analysis revealed that the transgenic plants with 0.3kb pro ::BAR showed reduced but comparable expression levels of BAR to those with 35S pro ::BAR. Moreover, the transcription activity of the 0.3 kb promoter could be increased by the fusion of an enhancer sequence. These results indicate that the 0.3 kb AtTCTP promoter can be used as a plant-derived constitutive promoter for the expression of selectable marker genes, which facilitates its use as an alternative to the 35S promoter for developing genetically engineered crops.
从 AtTCTP 表达分析中获得了一个植物来源的 0.3kb 组成型启动子,并成功应用于选择标记基因的表达,用于生产转基因匍匐翦股颖植物。分离和使用有效的启动子对于开发植物高效遗传转化载体系统至关重要,组成型启动子对于选择标记基因的表达特别有用。在这项研究中,我们从拟南芥翻译控制肿瘤蛋白(AtTCTP)基因的表达分析中表征了一个小尺寸的组成型启动子。组织化学和荧光 GUS 分析显示,AtTCTP 基因起始密码子上游的 303bp 区域在所有植物组织中均表现出强烈的 GUS 表达,与花椰菜花叶病毒 35S 启动子(35Spro)相比,其 GUS 活性约为 55%。为了检验该启动子在遗传工程作物开发中的可能应用,我们将含有 AtTCTP 0.3kb 启动子(0.3kbpro)的 pCAMBIA3301 载体导入匍匐翦股颖,该启动子与除草剂抗性 BAR 基因融合(0.3kb pro ::BAR)。我们的转化结果表明,成功地使用 0.3kb pro ::BAR 作为选择标记,生产出具有除草剂抗性的转基因匍匐翦股颖植物。Northern blot 分析显示,具有 0.3kb pro ::BAR 的转基因植物表现出降低但可比的 BAR 表达水平,与具有 35S pro ::BAR 的转基因植物相当。此外,增强子序列的融合可以增加 0.3kb 启动子的转录活性。这些结果表明,0.3kb AtTCTP 启动子可作为植物来源的组成型启动子,用于选择标记基因的表达,可作为开发遗传工程作物的 35S 启动子的替代物。