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线虫抗性基因Hs1pro-1的启动子可激活甜菜(Beta vulgaris L.)和拟南芥中对线虫有反应且在取食位点特异的基因表达。

The promoter of the nematode resistance gene Hs1pro-1 activates a nematode-responsive and feeding site-specific gene expression in sugar beet (Beta vulgaris L.) and Arabidopsis thaliana.

作者信息

Thurau Tim, Kifle Sirak, Jung Christian, Cai Daguang

机构信息

Institute of Crop Science and Plant Breeding, Christian Albrechts University of Kiel, Olshausenstrasse 40, 24098 Kiel, Germany.

出版信息

Plant Mol Biol. 2003 Jun;52(3):643-60. doi: 10.1023/a:1024887516581.

Abstract

The Hs1pro-1 gene confers resistance to the beet cyst nematode Heterodera schachtii in sugar beet (Beta vulgaris L.) on the basis of a gene-for-gene relationship. RNA-gel blot analysis revealed that the transcript of Hs1pro-1 was present in uninfected roots of resistant beet at low levels but increased by about fourfold one day after nematode infection. Treatments of plants with external stimuli including salicylic acid, jasmonic acid, gibberellic acid and abscisic acid as well as wounding or salt stress did not result in changes in the gene transcription, indicating de novo transcription of Hs1pro-1 upon nematode infection specifically. To study transcriptional regulation of Hs1pro-1 expression at the cellular level, a 3082 bp genomic fragment representing the Hs1pro-1 promoter, isolated from the YAC-DNA housing the Hs1pro-1 gene, was fused to the beta-glucuronidase reporter gene (1832prm1::GUS) and transformed into susceptible beet roots and Arabidopsis plants, respectively. Fluorometric and histochemical GUS assays on transgenic beet roots and Arabidopsis plants carrying the 1832prm1::GUS construct demonstrated that the Hs1pro-1 promoter is functional in both species and drives a nematode responsive and feeding site-specific GUS-expression. GUS activity was detected as early as at initiation of the nematode feeding sites and GUS staining was restricted to the nematode feeding sites. To delineate the regulatory domains of the Hs1pro-1 promoter, fusion genes with various 5' deletions of the Hs1pro-1 promoter and the GUS gene were constructed and analysed in transgenic beet roots as well. Cis elements responsible for feeding site-specific gene expression reside between -355 and +247 from the transcriptional initiation site of Hs1pro-1 whereas an enhancer region necessary for higher gene expression is located between -1199 and -705 of the promoter. The Hs1pro-1 promoter drives a nematode feeding site-specific GUS expression in both sugar beet and Arabidopsis suggesting a conserved mechanism of regulation of Hs1pro-1 expression in these two species.

摘要

基于基因对基因的关系,Hs1pro - 1基因赋予甜菜(Beta vulgaris L.)对甜菜孢囊线虫(Heterodera schachtii)的抗性。RNA凝胶印迹分析表明,Hs1pro - 1的转录本在未感染的抗性甜菜根中含量较低,但在被线虫感染一天后增加了约四倍。用包括水杨酸、茉莉酸、赤霉素和脱落酸在内的外部刺激物处理植物,以及进行创伤或盐胁迫处理,均未导致该基因转录发生变化,这表明Hs1pro - 就是一种基于基因对基因关系赋予甜菜(Beta vulgaris L.)对甜菜孢囊线虫(Heterodera schachtii)抗性的基因。RNA凝胶印迹分析显示,Hs1pro - 1的转录本在未感染的抗性甜菜根中含量较低,但在被线虫感染一天后增加了约四倍。用包括水杨酸、茉莉酸、赤霉素和脱落酸在内的外部刺激物处理植物,以及进行创伤或盐胁迫处理,均未导致该基因转录发生变化,这表明Hs1pro - 1仅在被线虫感染时从头转录。为了在细胞水平上研究Hs1pro - 1表达的转录调控,从包含Hs1pro - 1基因的酵母人工染色体(YAC) - DNA中分离出一个代表Hs1pro - 1启动子的3082 bp基因组片段,将其与β - 葡萄糖醛酸酶报告基因融合(1832prm1::GUS),并分别转化到易感甜菜根和拟南芥植物中。对携带1832prm1::GUS构建体的转基因甜菜根和拟南芥植物进行荧光和组织化学GUS分析表明,Hs1pro - 1启动子在这两个物种中均具有功能,并驱动线虫响应和取食位点特异性的GUS表达。早在线虫取食位点开始形成时就检测到了GUS活性,并且GUS染色仅限于线虫取食位点。为了确定Hs1pro - 1启动子的调控区域,还构建了具有Hs1pro - 1启动子各种5'端缺失的融合基因与GUS基因,并在转基因甜菜根中进行了分析。负责取食位点特异性基因表达的顺式元件位于Hs1pro - 1转录起始位点的 - 355至 + 247之间,而较高基因表达所需的增强子区域位于启动子的 - 1199至 - 705之间。Hs1pro - 1启动子在甜菜和拟南芥中均驱动线虫取食位点特异性的GUS表达,这表明这两个物种中Hs1pro - 1表达的调控机制具有保守性。 1仅在被线虫感染时从头转录。为了在细胞水平上研究Hs1pro - 1表达的转录调控,从包含Hs1pro - 1基因的酵母人工染色体(YAC) - DNA中分离出一个代表Hs1pro - 1启动子的3082 bp基因组片段,将其与β - 葡萄糖醛酸酶报告基因融合(1832prm ::GUS),并分别转化到易感甜菜根和拟南芥植物中。对携带1832prm1::GUS构建体的转基因甜菜根和拟南芥植物进行荧光和组织化学GUS分析表明,Hs1pro - 1启动子在这两个物种中均具有功能,并驱动线虫响应和取食位点特异性的GUS表达。早在线虫取食位点开始形成时就检测到了GUS活性,并且GUS染色仅限于线虫取食位点。为了确定Hs1pro - 1启动子的调控区域,还构建了具有Hs1pro - 1启动子各种5'端缺失的融合基因与GUS基因,并在转基因甜菜根中进行了分析。负责取食位点特异性基因表达的顺式元件位于Hs1pro - 1转录起始位点的 - 355至 + 247之间,而较高基因表达所需的增强子区域位于启动子的 - 1199至 - 705之间。Hs1pro - 1启动子在甜菜和拟南芥中均驱动线虫取食位点特异性的GUS表达,这表明这两个物种中Hs1pro - 1表达的调控机制具有保守性。

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