Bodeau J P, Walbot V
Department of Biological Sciences, Stanford University, CA 94305.
Mol Gen Genet. 1992 Jun;233(3):379-87. doi: 10.1007/BF00265434.
The putative maize transcription factor genes R and C1 are required for expression of reporter genes with promoters from the Bz1 and A1 genes, which encode enzymes required for anthocyanin biosynthesis in maize. Bz2 is another anthocyanin biosynthetic gene; we show that expression of a reporter gene from the Bz2 promoter also requires R and C1 when the fusion construct is introduced into maize kernels by particle gun bombardment. When electroporated into maize protoplasts from a suspension cell line not synthesizing anthocyanins, reporter genes with Bz2, Bz1, and A1 promoters are expressed only when both R and C1 expression plasmids are co-electroporated. Electroporation of R and C1 expression plasmids also induces the endogenous genes required for anthocyanin synthesis, resulting in pink protoplasts within 24 h. RNase protection analysis demonstrates that accumulation of mRNA from the endogenous Bz1 and Bz2 genes absolutely requires introduced R and C1. In time-course experiments there is a delay of 3-6 h before the Bz2 promoter is activated, supporting the proposed role for R- and C1-encoded proteins in transcriptional control. An excess of R relative to C1 suppresses expression of A1, Bz1, and Bz2 promoters, suggesting an interaction between the R and C1 proteins.
假定的玉米转录因子基因R和C1是使报告基因在具有来自Bz1和A1基因启动子的情况下得以表达所必需的,Bz1和A1基因编码玉米花青素生物合成所需的酶。Bz2是另一个花青素生物合成基因;我们发现,当通过粒子枪轰击将融合构建体导入玉米籽粒时,来自Bz2启动子的报告基因的表达也需要R和C1。当将具有Bz2、Bz1和A1启动子的报告基因电穿孔导入不合成花青素的悬浮细胞系的玉米原生质体时,只有当R和C1表达质粒共同电穿孔时,报告基因才会表达。R和C1表达质粒的电穿孔还诱导花青素合成合成所需需的内源基因,在24小时内产生粉红色原生质体。核糖核酸酶保护分析表明,内源Bz1和Bz2基因的mRNA积累绝对需要导入的R和C1。在时间进程实验中,Bz2启动子被激活前有3 - 6小时的延迟,这支持了R和C1编码的蛋白质在转录调控中的作用。相对于C1而言,过量的R会抑制A1、Bz1和Bz2启动子的表达,这表明R和C1蛋白之间存在相互作用。