Wang Li-Wei, He Mei-Wen, Guo Shi-Rong, Zhong Min, Shu Sheng, Sun Jin
Key Laboratory of Southern Vegetable Crop Genetic Improvement, Ministry of Agriculture, College of Horticulture, Nanjing Agricultural University, 210095, Nanjing, China.
Planta. 2017 May;245(5):889-908. doi: 10.1007/s00425-017-2650-7. Epub 2017 Jan 10.
The CsSAMs promoter is a salt-stress-inducible promoter containing three GT-1 elements that are sufficient for the salt-stress response. The transcription factor CsGT-3b was found to bind to the GT-1 element. The S-adenosyl-L-methionine synthase (SAMs) gene is among the functional genes induced during environmental stress. However, little is known about the regulatory mechanism and upstream regulators of this salt-inducible gene in cucumber plants. Thus, it is necessary to understand the characteristics of the SAMs gene by analyzing its promoter and transcription factors. In this study, we isolated and functionally analyzed a 1743-bp flanking fragment of the CsSAMs gene from Cucumis sativus. To examine promoter activity, the full-length promoter, as well as different promoter fragments, were fused to the β-glucuronidase (GUS) reporter gene and introduced into the tobacco genome. The full-length promoter displayed maximal promoter activity, whereas the P4 promoter, containing 321 bp of upstream sequence, showed no basal promoter activity. In addition, the CsSAMs promoter exhibited stress-inducible regulation rather than tissue-specific activity in transgenic tobacco. Histochemical analysis revealed strong GUS staining in leaves, stems, and roots, especially in the veins of leaves, the vascular bundle of stems, and root tip zones following NaCl stress. A transient expression assay confirmed that the 242-bp region (-1743 to -1500) was sufficient for the NaCl-stress response. Yeast one-hybrid assays further revealed interaction between the NaCl-response protein CsGT-3b and the GT-1 (GAAAAA) element within the 242-bp region. Taken together, we revealed the presence of four salt-stress-responsive elements (GT-1 cis-elements) in the CsSAMs promoter and identified a transcription factor, CsGT-3b, that specifically binds to this sequence. These results might help us better understand the intricate regulatory network of the cucumber SAMs gene.
CsSAMs启动子是一种盐胁迫诱导型启动子,包含三个对盐胁迫响应足够的GT-1元件。发现转录因子CsGT-3b与GT-1元件结合。S-腺苷-L-甲硫氨酸合成酶(SAMs)基因是环境胁迫期间诱导的功能基因之一。然而,关于黄瓜植株中这个盐诱导基因的调控机制和上游调节因子知之甚少。因此,有必要通过分析其启动子和转录因子来了解SAMs基因的特性。在本研究中,我们从黄瓜中分离并功能分析了CsSAMs基因的一个1743 bp侧翼片段。为检测启动子活性,将全长启动子以及不同的启动子片段与β-葡萄糖醛酸酶(GUS)报告基因融合,并导入烟草基因组。全长启动子显示出最大的启动子活性,而包含321 bp上游序列的P4启动子没有基础启动子活性。此外,CsSAMs启动子在转基因烟草中表现出胁迫诱导调节而非组织特异性活性。组织化学分析显示,在NaCl胁迫后,叶片、茎和根中,特别是在叶片叶脉、茎维管束和根尖区域有强烈的GUS染色。瞬时表达分析证实,242 bp区域(-1743至-1500)对NaCl胁迫响应足够。酵母单杂交分析进一步揭示了NaCl响应蛋白CsGT-3b与242 bp区域内的GT-1(GAAAAA)元件之间的相互作用。综上所述,我们揭示了CsSAMs启动子中存在四个盐胁迫响应元件(GT-1顺式元件),并鉴定了一个与该序列特异性结合的转录因子CsGT-3b。这些结果可能有助于我们更好地理解黄瓜SAMs基因复杂的调控网络。