Bodeau J P, Walbot V
Department of Biological Sciences, Stanford University, CA 94305, USA.
Plant Mol Biol. 1996 Nov;32(4):599-609. doi: 10.1007/BF00020201.
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.
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。