The National Key Facility for Crop Gene Resources and Genetic Improvement (NFCRI)/Key Laboratory of Grain Crop Genetic Resources Evaluation and Utilization, Institute of Crop Sciences, Chinese Academy of Agricultural Sciences, Beijing 100081, China.
Genes (Basel). 2023 May 25;14(6):1150. doi: 10.3390/genes14061150.
Promoters play a crucial role in controlling the spatial and temporal expression of genes at transcriptional levels in the process of higher plant growth and development. The spatial, efficient, and correct regulation of exogenous genes expression, as desired, is the key point in plant genetic engineering research. Constitutive promoters widely used in plant genetic transformation are limited because, sometimes, they may cause potential negative effects. This issue can be solved, to a certain extent, by using tissue-specific promoters. Compared with constitutive promoters, a few tissue-specific promoters have been isolated and applied. In this study, based on the transcriptome data, a total of 288 tissue-specific genes were collected, expressed in seven tissues, including the leaves, stems, flowers, pods, seeds, roots, and nodules of soybean (). KEGG pathway enrichment analysis was carried out, and 52 metabolites were annotated. A total of 12 tissue-specific genes were selected via the transcription expression level and validated through real-time quantitative PCR, of which 10 genes showed tissue-specific expression. The 3-kb 5' upstream regions of ten genes were obtained as putative promoters. Further analysis showed that all the 10 promoters contained many tissue-specific -elements. These results demonstrate that high-throughput transcriptional data can be used as effective tools, providing a guide for high-throughput novel tissue-specific promoter discovery.
启动子在高等植物生长发育过程中,在转录水平上控制基因的时空表达起着至关重要的作用。在外源基因表达的空间、高效和正确调控方面,这是植物基因工程研究的关键。在植物遗传转化中广泛应用的组成型启动子受到限制,因为有时它们可能会产生潜在的负面影响。通过使用组织特异性启动子,可以在一定程度上解决这个问题。与组成型启动子相比,已经分离并应用了一些组织特异性启动子。在本研究中,基于转录组数据,共收集了 288 个在大豆的 7 种组织(叶片、茎、花、荚、种子、根和根瘤)中表达的组织特异性基因。对其进行了 KEGG 途径富集分析,并注释了 52 种代谢物。通过转录表达水平选择了 12 个组织特异性基因,并通过实时定量 PCR 进行验证,其中 10 个基因表现出组织特异性表达。获得了这 10 个基因的全长 3-kb5'上游区作为可能的启动子。进一步分析表明,这 10 个启动子都包含许多组织特异性元件。这些结果表明,高通量转录组数据可以作为有效的工具,为高通量新型组织特异性启动子的发现提供指导。