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新型合成诱导启动子在水分胁迫下控制基因表达,具有转基因杨树绿色组织特异性。

Novel synthetic inducible promoters controlling gene expression during water-deficit stress with green tissue specificity in transgenic poplar.

机构信息

Center for Agricultural Synthetic Biology, University of Tennessee Institute of Agriculture, Knoxville, Tennessee, USA.

Department of Plant Sciences, University of Tennessee, Knoxville, Tennessee, USA.

出版信息

Plant Biotechnol J. 2024 Jun;22(6):1596-1609. doi: 10.1111/pbi.14289. Epub 2024 Jan 17.

DOI:10.1111/pbi.14289
PMID:38232002
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11123411/
Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ce1/11374062/87ee5cf36f25/PBI-22-1596-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ce1/11374062/3d615d31eea5/PBI-22-1596-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ce1/11374062/cc6c36ca30de/PBI-22-1596-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ce1/11374062/2e659dc537bd/PBI-22-1596-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ce1/11374062/2165f94ba87a/PBI-22-1596-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ce1/11374062/30dbfb2c2fed/PBI-22-1596-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ce1/11374062/f75b222044f1/PBI-22-1596-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ce1/11374062/87ee5cf36f25/PBI-22-1596-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ce1/11374062/3d615d31eea5/PBI-22-1596-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ce1/11374062/cc6c36ca30de/PBI-22-1596-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ce1/11374062/2e659dc537bd/PBI-22-1596-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ce1/11374062/2165f94ba87a/PBI-22-1596-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ce1/11374062/30dbfb2c2fed/PBI-22-1596-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ce1/11374062/f75b222044f1/PBI-22-1596-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ce1/11374062/87ee5cf36f25/PBI-22-1596-g004.jpg

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