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Identification and Functional Analysis of a Promoter Sequence for Phloem Tissue Specific Gene Expression from Populus trichocarpa

机译:来自杨树幼虫Populaem组织特异性基因表达的启动子序列的鉴定与功能分析

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Unlike xylem, which is primarily composed of dead cells in vascular bundles, phloem has living cells. It transports organic nutrients and long-distance communication signals to all parts of plants. In this report, we describe a promoter from Populus trichocarpa that drives strong gene expression in a phloem tissue-specific manner. First, we identified five candidate genes with strong expression in the developing phloem (DP) tissue from whole-transcriptome gene chip analyses of different tissue types of poplar. The putative promoter sequences of them were isolated and tested for their promoter activity in transgenic Arabidopsis plants. Among them, a promoter of the Potri.001G340200.1 gene (called the PtrDP3 promoter) was identified that has the strongest activity in phloem tissue. PtrDP3 promoter activity was found exclusively in phloem cells of the stem and root tissues of transgenic Arabidopsis plants, which was reproduced in the transgenic poplar plants. The phloemspecific activity of the PtrDP3 promoter was detected as early as in three-day-old seedlings and was not affected by abiotic stresses or exogenously applied plant hormones in transgenic Arabidopsis plants. Promoter deletion analysis identified a 100-bp regulatory region of the PtrDP3 promoter, which is necessary to drive phloem specific expression. This study provides evidence of a strong phloem-specific promoter that is suitable for phloem-specific biotechnological modifications in plants.
机译:与Xylem不同,主要由血管束中的死细胞组成,Phloem具有活细胞。它将有机营养素和长距离通信信号传输到植物的所有部分。在本报告中,我们描述了来自杨树的杨树科氏菌的启动子,以韧皮组织特异性方式驱动强基因表达。首先,我们鉴定了来自不同组织类型的杨树的全转录组基因芯片分析的验磷脂(DP)组织中具有强烈表达的五种候选基因。将其调用的启动子序列分离并测试其在转基因拟南芥植物中的启动子活性。其中,鉴定了Potri.001G340200.1基因的启动子(称为PTRDP3启动子),其具有韧皮肽组织中最强的活性。 PTRDP3启动子活性仅在转基因拟南芥植物的茎和根组织的韧皮细胞中发现,该植物在转基因杨树植物中再现。早在三天龄幼苗中检测到PTRDP3启动子的磷脂特异性,并且在转基因拟南芥植物中不受非生物应激或外源应用植物激素的影响。启动子缺失分析鉴定了PTRDP3启动子的100bp调节区,这是驱动Phloem特异性表达所必需的。本研究提供了一种强大的韧皮肽特异性启动子的证据,适用于植物中的韧皮植物特异性生物技术修饰。

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