Department of Crop Genomics & Genetic Improvement, Biotechnology Research Institute, Chinese Academy of Agricultural Sciences, 12 ZhongGuanCun South Street, Beijing, China.
Key Laboratory of Crop Biology of Anhui Province, Anhui Agricultural University, Hefei, China.
Plant Cell Physiol. 2018 Oct 1;59(10):1942-1955. doi: 10.1093/pcp/pcy110.
Tissue-specific promoters play an important role in plant molecular farming. Here, we describe a strategy to modify the tissue specificity of a maize embryo-specific bidirectional promoter PZmBD1. Six types of cis-elements, i.e. RY repeats (R), GCN4 (G), the prolamin box (P), Skn-1 (S), and the ACGT and AACA (A) motifs, were collected and fused to PZmBD1 to generate eight chimeric putative bidirectional promoters. Qualitative and quantitative analysis of reporter genes driven by the promoters showed that two promoters exhibited high seed-specific bidirectional activity in maize transient and stable transformed systems. The stronger one was chosen and fused to the intergenic region of two gene clusters consisting of four anthocyanin biosynthesis-related genes (ZmBz1, ZmBz2, ZmC1 and ZmR2) and seven reporter genes, resulting in the first embryo and endosperm anthocyanin-rich purple maize. Anthocyanin analysis showed that the total anthocyanin content reaches 2,910 mg kg-1 DW in transgenic maize and cyanidin is the major anthocyanin in transgenic maize, as in natural varieties. The expression profile analysis of endogenous genes showed that the anthocyanin biosynthesis pathway was activated by two transgenic transcription factor genes ZmC1 and ZmR2. Our results indicate that both the modification strategy and these functionally characterized tissue-specific bidirectional promoters generated could be used for genetic research and development of plant biotechnology products. The anthocyanin-rich purple maize could provide economic natural colorants for the food and beverage industry, and valuable germplasm for developing anthocyanin-rich fresh corn.
组织特异性启动子在植物分子农业中起着重要作用。在这里,我们描述了一种修饰玉米胚胎特异性双向启动子 PZmBD1 组织特异性的策略。收集了六种顺式元件,即 RY 重复序列(R)、GCN4(G)、类蛋白盒(P)、Skn-1(S)以及 ACGT 和 AACA(A)基序,并将其融合到 PZmBD1 中,生成了八种嵌合的假定双向启动子。通过启动子驱动报告基因的定性和定量分析表明,两种启动子在玉米瞬时和稳定转化系统中表现出高种子特异性双向活性。选择其中较强的一种,并将其与由四个花青素生物合成相关基因(ZmBz1、ZmBz2、ZmC1 和 ZmR2)和七个报告基因组成的两个基因簇的基因间区融合,得到了第一个胚和胚乳富含花青素的紫色玉米。花青素分析表明,转基因玉米中的总花青素含量达到 2910mgkg-1DW,并且在转基因玉米中,与天然品种一样,矢车菊素是主要的花青素。内源基因表达谱分析表明,花青素生物合成途径被两个转基因转录因子基因 ZmC1 和 ZmR2 激活。我们的结果表明,修饰策略和这些功能表征的组织特异性双向启动子都可用于遗传研究和植物生物技术产品的开发。富含花青素的紫色玉米可为食品和饮料行业提供经济的天然色素,并为开发富含花青素的鲜食玉米提供有价值的种质资源。