Kusaba M, Takahashi Y, Nagata T
Department of Biological Sciences, Graduate School of Science, University of Tokyo, Japan.
Plant Physiol. 1996 Aug;111(4):1161-7. doi: 10.1104/pp.111.4.1161.
The expression of parA, an auxin-regulated gene expressed during the culture of tobacco (Nicotiana tabacum L.) mesophyll protoplasts, is induced by cadmium. To identify the cadmium-responsive element, we examined the parA promoter using the GUS reporter gene. Cadmium responsiveness was retained in a 5' deletion of the parA promoter to -78 bp, but it was nullified by further deletion to -49bp, which implies that the region -49 to -78 bp contained a cadmium-responsive element. This region contains a sequence similar to as-1, an enhancer sequence from the cauliflower mosaic virus 35S RNA promoter that binds the nuclear factor ASF-1. We named the sequence in the parA promoter pas. Gel-shift assays revealed that pas and as-1 compete for the same DNA-binding nuclear protein(s). Since pentamers of either pas and as-1 were able to confer cadmium responsiveness on a minimal promoter but mutant as-1 was not, we propose that pas and as-1 are involved in cadmium-responsive gene expression. Neither pas nor as-1 conferred responsiveness to copper. The specificity of this response, involving the function of as-1-related elements including pas, is discussed.
parA是烟草(Nicotiana tabacum L.)叶肉原生质体培养过程中表达的一种生长素调节基因,其表达受镉诱导。为了鉴定镉反应元件,我们使用GUS报告基因检测了parA启动子。parA启动子的5'端缺失至-78 bp时仍保留镉反应性,但进一步缺失至-49 bp时则丧失,这表明-49至-78 bp区域包含一个镉反应元件。该区域包含一个与as-1相似的序列,as-1是花椰菜花叶病毒35S RNA启动子的增强子序列,可结合核因子ASF-1。我们将parA启动子中的该序列命名为pas。凝胶迁移实验表明,pas和as-1竞争相同的DNA结合核蛋白。由于pas和as-1的五聚体均能赋予最小启动子镉反应性,而突变型as-1则不能,因此我们认为pas和as-1参与了镉反应基因的表达。pas和as-1均未赋予对铜的反应性。本文讨论了这种涉及包括pas在内的as-1相关元件功能的反应特异性。