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伤口诱导型核因子与甘露碱合成酶2'启动子伤口响应元件的序列特异性相互作用。

Sequence-specific interactions of wound-inducible nuclear factors with mannopine synthase 2' promoter wound-responsive elements.

作者信息

Ni M, Cui D, Gelvin S B

机构信息

Department of Biological Sciences, Purdue University, West Lafayette, IN 47907, USA.

出版信息

Plant Mol Biol. 1996 Jan;30(1):77-96. doi: 10.1007/BF00017804.

Abstract

A 318 bp mannopine synthase 2' (mas2') promoter element from the T-DNA of Agrobacterium tumefacians 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.

摘要

来自根癌土壤杆菌T-DNA的一段318 bp甘露碱合成酶2'(mas2')启动子元件,可在转基因烟草植株中指导连接的uidA基因的创伤诱导型和根优先表达。培养基中的蔗糖可进一步增强创伤诱导性。启动子缺失分析表明,蔗糖增强作用由一个从-318延伸至-213的区域赋予。DNase I足迹分析表明,该区域富含A/T的DNA序列受到烟草核因子的保护。当分别置于CaMV 35S增强子下游或截短的(-209)CaMV 35S启动子上游时,从-103至+66以及从-213至-138的区域分别指导连接的uidA基因的创伤诱导型表达。DNase I足迹分析表明,来自受伤烟草叶片的蛋白质特异性结合到mas2'TATA框下游的三个相邻基序上。除了由上游创伤响应元件与来自受伤或未受伤烟草叶片的蛋白质复合形成的常见滞后条带外,当该元件与来自受伤叶片的蛋白质一起孵育时,还观察到两个独特的滞后条带。甲基化干扰分析还鉴定出一个由启动子元件和专门来自受伤烟草叶片的核因子组成的独特基序。我们提出了一个模型来描述核因子与mas2'启动子元件在创伤诱导型基因表达中的作用。

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