首页> 外文期刊>Plant Molecular Biology >SEQUENCE-SPECIFIC INTERACTIONS OF WOUND-INDUCIBLE NUCLEAR FACTORS WITH MANNOPINE SYNTHASE 2' PROMOTER WOUND-RESPONSIVE ELEMENTS
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SEQUENCE-SPECIFIC INTERACTIONS OF WOUND-INDUCIBLE NUCLEAR FACTORS WITH MANNOPINE SYNTHASE 2' PROMOTER WOUND-RESPONSIVE ELEMENTS

机译:伤口诱导型核因子与甘露肽合酶2'启动子伤口反应元件的序列特异性相互作用

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摘要

A 318 bp mannopine synthase 2' (mas2') promoter element from the T-DNA of Agrobacterium tumefaciens can direct wound-inducible and root-preferential expression of a linked uidA gene in transgenic tobacco plants. Wound inducibility is further enhanced by sucrose in the medium. Promoter deletion analysis indicated that the sucrose enhancement is conferred by a region extending from -318 to -213. DNase I footprinting indicated that an A/T-rich DNA sequence in this region is protected by tobacco nuclear factors. Regions extending from -103 to +66 and from -213 to -138 directed wound-inducibile expression of a linked uidA gene when placed downstream of a CaMV 35S enhancer or upstream of a truncated (-209) CaMV 35S promoter, respectively. DNase I footprinting analyses indicated that proteins from wounded tobacco leaves specifically bound to three contiguous motifs downstream of the mas2' TATA box. In addition to a common retarded band formed by the upstream wound-responsive element complexed with proteins from either wounded or unwounded tobacco leaves, two unique retarded bands were observed when this element was incubated with protein from wounded leaves. Methylation interference analysis additionally identified an unique motif composed of promoter elements and nuclear factors derived specifically from wounded tobacco leaves. We propose a model to describe the involvement of nuclear factors with mas2' promoter elements in wound-inducible gene expression. [References: 50]
机译:来自根癌土壤杆菌T-DNA的318 bp mannopine合酶2'(mas2')启动子元件可以指导连接的uidA基因在转基因烟草植物中的伤口诱导和根系优先表达。培养基中的蔗糖进一步增强了伤口的诱导能力。启动子缺失分析表明,蔗糖增强是由从-318到-213延伸的区域赋予的。 DNase I足迹表明该区域富含A / T的DNA序列受烟草核因子保护。当分别位于CaMV 35S增强子的下游或截短的(-209)CaMV 35S启动子的上游时,从-103至+66和-213至-138的区域分别指导链接的uidA基因的伤口诱导表达。 DNase I足迹分析表明,来自受伤烟叶的蛋白质与mas2'TATA盒下游的三个连续基序特异性结合。除了上游伤口反应元件与受伤或未伤口烟草叶片的蛋白质复合形成的共同的阻滞带外,当将该元件与伤口叶片的蛋白质孵育时,观察到两个独特的阻滞带。甲基化干扰分析还确定了一个独特的基序,该基序由启动子元素和专门从伤口烟叶衍生的核因子组成。我们提出一种模型来描述核因子与mas2'启动子元件在伤口诱导基因表达中的参与。 [参考:50]

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