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保守的顺式作用启动子元件是根癌土壤杆菌接合转移基因密度依赖性转录所必需的。

Conserved cis-acting promoter elements are required for density-dependent transcription of Agrobacterium tumefaciens conjugal transfer genes.

作者信息

Fuqua C, Winans S C

机构信息

Department of Biology, Trinity University, San Antonio, Texas 78212, USA.

出版信息

J Bacteriol. 1996 Jan;178(2):435-40. doi: 10.1128/jb.178.2.435-440.1996.

Abstract

Ti plasmids of Agrobacterium tumefaciens, in addition to transferring oncogenic DNA to the nuclei of infected plant cells, can conjugally transfer between agrobacteria. Conjugation of wide-host-range octopine-type Ti plasmids requires a tumor-released arginine derivative called octopine. Octopine stimulates expression of the traR gene, whose product directly activates other tra genes in the presence of an acylated homoserine lactone called Agrobacterium autoinducer (AAI). We have localized the transcription starts of three tra promoters and find conserved elements (tra boxes) at virtually identical positions upstream of each promoter. Disruption of these tra boxes abolished induction of each promoter. Deletion analysis of the traI promoter indicates that tra boxes are the only upstream elements required for transcriptional activation. Since Ti plasmid donor cells both produce and respond to AAI, we tested whether expression of tra promoters was enhanced by high concentrations of bacteria. Both tra gene expression and conjugation itself were strongly stimulated either by high donor densities or by exogenous AAI.

摘要

根癌土壤杆菌的Ti质粒,除了将致癌DNA转移到受感染植物细胞的细胞核外,还能在土壤杆菌之间进行接合转移。广宿主范围章鱼碱型Ti质粒的接合需要一种名为章鱼碱的肿瘤释放精氨酸衍生物。章鱼碱刺激traR基因的表达,在一种名为土壤杆菌自诱导物(AAI)的酰化高丝氨酸内酯存在的情况下,其产物直接激活其他tra基因。我们已经定位了三个tra启动子的转录起始位点,并在每个启动子上游几乎相同的位置发现了保守元件(tra框)。这些tra框的破坏消除了每个启动子的诱导。traI启动子的缺失分析表明,tra框是转录激活所需的唯一上游元件。由于Ti质粒供体细胞既产生AAI又对其作出反应,我们测试了高浓度细菌是否会增强tra启动子的表达。高供体密度或外源性AAI均强烈刺激tra基因表达和接合本身。

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