Lin Y, Hwang C F, Brown J B, Cheng C L
Department of Biological Sciences, University of Iowa, Iowa City 52242.
Plant Physiol. 1994 Oct;106(2):477-84. doi: 10.1104/pp.106.2.477.
Nitrate reductase (NR) is the first enzyme in nitrate assimilation, a critical process for plant survival. The regulation of NR gene expression is complex, involving both internal and external factors. Of these, nitrate induction of NR gene expression has been studied most extensively and is well conserved among bacteria, fungi, and higher plants. We are interested in understanding the mechanism of nitrate induction of higher plant NR genes. Here we describe promoter analyses of the 5' flanking regions of the Arabidopsis NR genes, NR1 and NR2, with respect to nitrate induction of gene expression. To facilitate these analyses, a nitrate induction procedure using T1 transgenic tobacco plants was established. Approximately 1.5-kb 5' flanking regions of the two Arabidopsis NR genes (NR1 and NR2) were fused to a reporter gene and its expression in transgenic plants was analyzed. Deletion analyses of these regions show that 238- and 188-bp 5' flanking regions of the NR1 and NR2, respectively, contain sequences responsive to nitrate induction.
硝酸还原酶(NR)是硝酸盐同化过程中的首个酶,而硝酸盐同化是植物生存的关键过程。NR基因表达的调控较为复杂,涉及内部和外部因素。其中,硝酸盐对NR基因表达的诱导作用研究最为广泛,且在细菌、真菌和高等植物中高度保守。我们感兴趣的是了解高等植物NR基因硝酸盐诱导的机制。在此,我们描述了拟南芥NR基因NR1和NR2的5'侧翼区域关于基因表达的硝酸盐诱导的启动子分析。为便于这些分析,建立了使用T1转基因烟草植株的硝酸盐诱导程序。将两个拟南芥NR基因(NR1和NR2)约1.5 kb的5'侧翼区域与一个报告基因融合,并分析其在转基因植物中的表达。对这些区域的缺失分析表明,NR1和NR2的5'侧翼区域分别有238 bp和188 bp包含对硝酸盐诱导有响应的序列。