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Unwounded plants elicit Agrobacterium vir gene induction and T-DNA transfer: transformed plant cells produce opines yet are tumour free

机译:未受伤害的植物引发农杆菌病毒基因诱导和T-DNA转移:转化的植物细胞可产生鸦片,但无肿瘤

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摘要

Agrobacterium tumefaciens is well known to cause crown gall tumours at plant wound sites and to benefit from this plant association by obtaining nutrients called opines that are produced by these tumours. Tumourigenesis requires expression of the vir regulon in response to chemical signals that are thought to be released from wound sites. Here, we examine chemical interactions between A. tumefaciens and unwounded plants. To determine whether unwounded plants can release significant amounts of vir gene inducers, we constructed an A. tumefaciens strain carrying a PvirB-gfp fusion. This fusion was strongly induced by co-culture with tobacco seedlings that have been germinated without any intentional wounding. The release of phenolic vir gene inducers was confirmed by GC/MS analysis. We also constructed a strain containing the gfp reporter located on an artificial T-DNA and expressed from a plant promoter. A. tumefaciens efficiently transferred this T-DNA into cells of unwounded plants in the absence of exogenous vir gene inducers. Many cells of seedlings colonized by the bacteria also produced octopine, which was detected using a Pocc-gfp reporter strain. This indicates transfer of the native T-DNA. However, these transformed plant cells did not form tumours. These results suggest that successful colonization of plants by A. tumefaciens, including T-DNA transfer and opine production, does not require wounding and does not necessarily cause cell proliferation. Transformation of plant cells without inciting tumours may represent a colonization strategy for this pathogen that has largely been overlooked.
机译:众所周知,根癌土壤杆菌可在植物伤口部位引起冠gall瘤,并通过获得由这些肿瘤产生的称为阿片素的营养物而从这种植物结合中受益。肿瘤发生需要响应被认为从伤口部位释放的化学信号表达vir regulon。在这里,我们检查了根癌农杆菌和未受伤植物之间的化学相互作用。为了确定未受伤的植物是否可以释放大量的vir基因诱导剂,我们构建了携带PvirB-gfp融合蛋白的根癌农杆菌菌株。通过与发芽的烟草幼苗共培养而没有任何故意伤害,强烈诱导了这种融合。酚vir基因诱导剂的释放通过GC / MS分析确认。我们还构建了包含位于人工T-DNA上并从植物启动子表达的gfp报告基因的菌株。在不存在外源vir基因诱导剂的情况下,根癌土壤杆菌有效地将该T-DNA转移至未受伤植物的细胞中。被细菌繁殖的许多幼苗细胞也产生了章鱼碱,这是用Pocc-gfp报告株检测到的。这表明天然T-DNA的转移。但是,这些转化的植物细胞没有形成肿瘤。这些结果表明,根癌农杆菌成功地将植物定植,包括T-DNA转移和阿片生成,并不需要受伤,也不一定会引起细胞增殖。在不引发肿瘤的情况下转化植物细胞可能代表了这种病原体的定殖策略,而这种定殖策略在很大程度上被忽视了。

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