Center for Agricultural Synthetic Biology, University of Tennessee Institute of Agriculture, Knoxville, Tennessee, USA.
Department of Plant Sciences, University of Tennessee, Knoxville, Tennessee, USA.
Plant Biotechnol J. 2024 Jun;22(6):1596-1609. doi: 10.1111/pbi.14289. Epub 2024 Jan 17.
Synthetic promoters may be designed using short cis-regulatory elements (CREs) and core promoter sequences for specific purposes. We identified novel conserved DNA motifs from the promoter sequences of leaf palisade and vascular cell type-specific expressed genes in water-deficit stressed poplar (Populus tremula × Populus alba), collected through low-input RNA-seq analysis using laser capture microdissection. Hexamerized sequences of four conserved 20-base motifs were inserted into each synthetic promoter construct. Two of these synthetic promoters (Syn2 and Syn3) induced GFP in transformed poplar mesophyll protoplasts incubated in 0.5 M mannitol solution. To identify effect of length and sequence from a valuable 20 base motif, 5' and 3' regions from a basic sequence (GTTAACTTCAGGGCCTGTGG) of Syn3 were hexamerized to generate two shorter synthetic promoters, Syn3-10b-1 (5': GTTAACTTCA) and Syn3-10b-2 (3': GGGCCTGTGG). These promoters' activities were compared with Syn3 in plants. Syn3 and Syn3-10b-1 were specifically induced in transient agroinfiltrated Nicotiana benthamiana leaves in water cessation for 3 days. In stable transgenic poplar, Syn3 presented as a constitutive promoter but had the highest activity in leaves. Syn3-10b-1 had stronger induction in green tissues under water-deficit stress conditions than mock control. Therefore, a synthetic promoter containing the 5' sequence of Syn3 endowed both tissue-specificity and water-deficit inducibility in transgenic poplar, whereas the 3' sequence did not. Consequently, we have added two new synthetic promoters to the poplar engineering toolkit: Syn3-10b-1, a green tissue-specific and water-deficit stress-induced promoter, and Syn3, a green tissue-preferential constitutive promoter.
合成启动子可以使用短的顺式调控元件(CREs)和核心启动子序列来设计,用于特定目的。我们从受水分胁迫的杨树(Populus tremula × Populus alba)叶栅栏组织和脉管细胞类型特异性表达基因的启动子序列中,通过激光捕获显微切割的低输入 RNA-seq 分析,鉴定出了新的保守 DNA 基序。将四个保守的 20 碱基基序的六聚体序列插入每个合成启动子构建体中。这两个合成启动子(Syn2 和 Syn3)在转化的杨树叶肉原生质体中诱导 GFP 的表达,这些原生质体在 0.5 M 甘露醇溶液中孵育。为了鉴定一个有价值的 20 碱基基序的长度和序列的影响,从 Syn3 的基本序列(GTTAACTTCAGGGCCTGTGG)的 5'和 3'区域中六聚化生成两个较短的合成启动子,Syn3-10b-1(5':GTTAACTTCA)和 Syn3-10b-2(3':GGGCCTGTGG)。这些启动子的活性在植物中与 Syn3 进行了比较。Syn3 和 Syn3-10b-1 在停止浇水 3 天后的瞬时农杆菌浸润的烟草原生质体叶片中特异性诱导。在稳定的转基因杨树中,Syn3 表现为组成型启动子,但在叶片中活性最高。Syn3-10b-1 在缺水胁迫条件下绿色组织的诱导作用强于对照。因此,含有 Syn3 5'序列的合成启动子赋予了转基因杨树组织特异性和缺水诱导性,而 3'序列则没有。因此,我们向杨树工程工具包中添加了两个新的合成启动子:Syn3-10b-1,一个绿色组织特异性和缺水胁迫诱导启动子,以及 Syn3,一个绿色组织优先组成型启动子。