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玉米青铜2基因启动子的结构与调控

Structure and regulation of the maize Bronze2 promoter.

作者信息

Bodeau J P, Walbot V

机构信息

Department of Biological Sciences, Stanford University, CA 94305, USA.

出版信息

Plant Mol Biol. 1996 Nov;32(4):599-609. doi: 10.1007/BF00020201.

Abstract

The maize Bronze2 (Bz2) gene encodes a glutathione S-transferase that is required for anthocyanin pigment accumulation. Two classes of regulatory proteins, R and C1, are required for transcriptional activation of Bz2 and several additional structural genes. Functional domains of the Bz2 promoter were identified using Bz2 promoter-driven luciferase reporter genes electroporated into maize protoplasts together with R and C1 expression plasmids. Complete regulation was conferred by 224 nt of the Bz2 promoter. Within this region at least two separable regions are independently capable of conferring regulation by R and C1. Predicted regulatory elements corresponding to two classes of sequence motifs, the Myb-box homologous 'C1-motif', TAACTG/CAGTTA, and the G-box and E-box homologous 'R-motif', CACGTG, were shown to be important for full R and C1 activation of the Bz2 promoter. Expression of reconstructed Bz2 genes with mutated promoters was quantified using RNase protection, and this analysis confirmed results obtained using reporter genes.

摘要

玉米青铜2(Bz2)基因编码一种谷胱甘肽S-转移酶,它是花青素色素积累所必需的。两类调节蛋白,即R和C1,是Bz2及其他几个结构基因转录激活所必需的。通过将Bz2启动子驱动的荧光素酶报告基因与R和C1表达质粒一起电穿孔导入玉米原生质体,鉴定了Bz2启动子的功能结构域。Bz2启动子的224个核苷酸赋予了完全的调控作用。在该区域内,至少有两个可分离的区域能够独立地赋予R和C1调控作用。预测的对应于两类序列基序的调控元件,即Myb-box同源的“C1基序”TAACTG/CAGTTA,以及G-box和E-box同源的“R基序”CACGTG,对Bz2启动子的完全R和C1激活很重要。使用核糖核酸酶保护法定量分析了具有突变启动子的重组Bz2基因的表达,该分析证实了使用报告基因获得的结果。

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