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植物中高表达基因的合成 DNA 启动子的比较分析。

Comparative analysis of synthetic DNA promoters for high-level gene expression in plants.

机构信息

KTRDC, College of Agriculture, University of Kentucky, Lexington, KY, 40546, USA,

出版信息

Planta. 2014 Oct;240(4):855-75. doi: 10.1007/s00425-014-2135-x. Epub 2014 Aug 5.

Abstract

We have designed two near- constitutive and stress-inducible promoters (CmYLCV9.11 and CmYLCV4); those are highly efficient in both dicot and monocot plants and have prospective to substitute the CaMV 35S promoter. We performed structural and functional studies of the full-length transcript promoter from Cestrum yellow leaf curling virus (CmYLCV) employing promoter/leader deletion and activating cis-sequence analysis. We designed a 465-bp long CmYLCV9.11 promoter fragment (-329 to +137 from transcription start site) that showed enhanced promoter activity and was highly responsive to both biotic and abiotic stresses. The CmYLCV9.11 promoter was about 28-fold stronger than the CaMV35S promoter in transient and stable transgenic assays using β-glucuronidase (GUS) reporter gene. The CmYLCV9.11 promoter also demonstrated stronger activity than the previously reported CmYLCV promoter fragments, CmpC (-341 to +5) and CmpS (-349 to +59) in transient systems like maize protoplasts and onion epidermal cells as well as transgenic systems. A good correlation between CmYLCV9.11 promoter-driven GUS-accumulation/enzymatic activities with corresponding uidA-mRNA level in transgenic tobacco plants was shown. Histochemical (X-Gluc) staining of transgenic seedlings, root and floral parts expressing the GUS under the control of CmYLCV9.11, CaMV35S, CmpC and CmpS promoters also support the above findings. The CmYLCV9.11 promoter is a constitutive promoter and the expression level in tissues of transgenic tobacco plants was in the following order: root > leaf > stem. The tobacco transcription factor TGA1a was found to bind strongly to the CmYLCV9.11 promoter region, as shown by Gel-shift assay and South-Western blot analysis. In addition, the CmYLCV9.11 promoter was regulated by a number of abiotic and biotic stresses as studied in transgenic Arabidopsis and tobacco plants. The newly derived CmYLCV9.11 promoter is an efficient tool for biotechnological applications.

摘要

我们设计了两个近组成型和应激诱导启动子(CmYLCV9.11 和 CmYLCV4);它们在双子叶和单子叶植物中都非常高效,有潜力替代 CaMV 35S 启动子。我们对全长转录启动子进行了结构和功能研究,使用启动子/先导序列缺失和激活顺式序列分析方法研究了西番莲黄花叶卷曲病毒(CmYLCV)的全长转录本启动子。我们设计了一个 465 个碱基对长的 CmYLCV9.11 启动子片段(从转录起始位点的-329 到+137),该启动子片段表现出增强的启动子活性,并且对生物和非生物胁迫高度响应。在使用β-葡萄糖醛酸酶(GUS)报告基因的瞬时和稳定转基因试验中,CmYLCV9.11 启动子比 CaMV35S 启动子强约 28 倍。在瞬时系统(如玉米原生质体和洋葱表皮细胞)和转基因系统中,CmYLCV9.11 启动子也显示出比先前报道的 CmYLCV 启动子片段 CmpC(-341 至+5)和 CmpS(-349 至+59)更强的活性。在转基因烟草植物中,CmYLCV9.11 启动子驱动的 GUS 积累/酶活性与相应的 uidA-mRNA 水平之间存在良好的相关性。在控制下,CmYLCV9.11、CaMV35S、CmpC 和 CmpS 启动子表达的转基因幼苗、根和花部的组织化学(X-Gluc)染色也支持上述发现。烟草转录因子 TGA1a 被发现能够与 CmYLCV9.11 启动子区域强烈结合,凝胶迁移分析和西南印迹分析表明了这一点。此外,在转基因拟南芥和烟草植物中研究表明,CmYLCV9.11 启动子受到多种非生物和生物胁迫的调控。新衍生的 CmYLCV9.11 启动子是生物技术应用的有效工具。

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