Nishiuchi T, Nakamura T, Abe T, Kodama H, Nishimura M, Iba K
Department of Biology, Faculty of Science, Kyushu University, Fukuoka, Japan.
Plant Mol Biol. 1995 Nov;29(3):599-609. doi: 10.1007/BF00020987.
The Arabidopsis FAD7 gene encodes a chloroplast omega-3 fatty acid desaturase that catalyzes the desaturation of lipid-linked dienoic fatty acids (18:2 and 16:2). An 825 bp FAD7 promoter fragment upstream from the transcriptional start point contained several short sequences which were homologous to the cis-elements (box II, G-box, etc.) conserved in many light-responsive genes. We introduced the FAD7 promoter fused to the beta-glucuronidase (GUS) or the luciferase (LUC) reporter gene into tobacco plants. The -825 promoter sequence conferred tissue-specific and light-responsive expression to both these reporter genes in transgenic tobacco, indicating that these expressions of the FAD7 gene were regulated mainly at the transcriptional level. Histochemical GUS staining showed that the activity of the FAD7 promoter is restricted to the tissues with chloroplast-containing cells although the staining was noticeably absent in the chloroplast-containing cells associated with vascular systems. The 5' deletion experiments of the promoter revealed that the -362/-166 region, containing two putative box II sequences, was responsible for the tissue-specific and light-responsive expression of the FAD7 gene.
拟南芥FAD7基因编码一种叶绿体ω-3脂肪酸去饱和酶,该酶催化脂联二烯脂肪酸(18:2和16:2)的去饱和反应。转录起始点上游825 bp的FAD7启动子片段包含几个短序列,这些序列与许多光响应基因中保守的顺式元件(框II、G框等)同源。我们将与β-葡萄糖醛酸酶(GUS)或荧光素酶(LUC)报告基因融合的FAD7启动子导入烟草植株。-825启动子序列赋予这两个报告基因在转基因烟草中的组织特异性和光响应性表达,表明FAD7基因的这些表达主要在转录水平受到调控。组织化学GUS染色显示,FAD7启动子的活性仅限于含有叶绿体的细胞的组织,尽管在与维管系统相关的含有叶绿体的细胞中明显没有染色。启动子的5'缺失实验表明,包含两个假定框II序列的-362 / -166区域负责FAD7基因的组织特异性和光响应性表达。