Yu Peng, Xueqin Guo, Yawei Fan, Han Liu, Leiqian Sun, Di Liu, Hui Li, Xin Wang, Hongli Guo, Hai Lu
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引用次数: 0
摘要
基因表达受转录因子与启动子中顺式元件结合的调控。然而,用于基因工程的高效顺式元件却鲜有报道。在这项研究中,我们在 PtoCP1 启动子中发现了一个 11 bp 的顺式元件,它能驱动杨树中强组成型基因的表达。我们克隆了 PtoCP1 基因翻译起始位点上游的 2270 bp 启动子区域,并将其命名为 ProPtoCP1。该启动子控制拟南芥幼苗根、叶和茎中 GUS 报告基因的表达。根据顺式元件的位置和密度,PtoCP1 启动子通过 5'-end 删除被分为四个片段。GUS 染色和 RT-qPCR 发现在 -466 至 -441 bp 处有一个对基因表达至关重要的关键顺式元件。进一步分析表明,MYB-TGACG 顺式元件是一个正调控因子,而单独的 MYB 或 TGACG 都不能驱动基因表达。这项研究加深了我们对顺式元件对基因表达调控的理解,并为基因工程提供了一种有价值的工具。
Identifying a cis-element in PtoCP1 promoter for efficiently controlling constitutive gene expression in Populus tomentosa.
Gene expression is regulated by transcription factors binding to cis-elements in promoters. However, efficient cis-elements for genetic engineering are rarely reported. In this study, we identified an 11 bp cis-element in the PtoCP1 promoter that drives strong constitutive gene expression in Populus tomentosa. A 2,270 bp promoter region upstream of the PtoCP1 gene's translation start site was cloned and named ProPtoCP1. This promoter controls GUS reporter gene expression in the roots, leaves, and stems of Arabidopsis seedlings. Based on the location and density of cis-elements, the PtoCP1 promoter was divided into four fragments by 5'-end deletions. GUS staining and RT-qPCR revealed a key cis-element at -466 to -441 bp essential for gene expression. Further analysis showed that the MYB-TGACG cis-element is a positive regulator, whereas neither MYB nor TGACG alone drove gene expression. This study enhances our understanding of gene expression regulation by cis-elements and provides a valuable tool for genetic engineering.