Kagaya Y, Nakamura H, Hidaka S, Ejiri S, Tsutsumi K
Institute for Cell Biology and Genetics, Faculty of Agriculture, Iwate University, Japan.
Mol Gen Genet. 1995 Oct 25;248(6):668-74. doi: 10.1007/BF02191706.
The rice genome contains at least four separate loci that encode aldolase isozymes. Among these, the aldolase P (AldP) gene, a nuclear gene coding for chloroplast aldolase, is expressed predominantly in the leaf blade mesophyll cells in rice. To dissect promoter elements that regulate such tissue- or cell type-specific expression, we constructed various AldP promoter-beta-glucuronidase (GUS) fusion genes and transferred them into Nicotiana tabacum (tobacco) plants. Analysis of GUS activities in the transgenic tobacco revealed the presence of at least two elements within 2.0 kb AldP promoter region. One is located within the segment from position -2.0 kb to -1.2 kb and acts as a negative element. The other is a positive element located between -1.2 kb and -0.31 kb that confers developmentally regulated, mesophyll cell-specific expression. In addition, the 1.2 kb rice promoter segment flanking the transcription start site contains an element(s) that serves as target for light induction in tobacco. The results suggest that the AldP gene promoter of rice, a monocot promoter, can function in an essentially physiological manner in the dicot tobacco plant.
水稻基因组至少包含四个编码醛缩酶同工酶的独立基因座。其中,醛缩酶P(AldP)基因是一个编码叶绿体醛缩酶的核基因,在水稻叶片叶肉细胞中大量表达。为了剖析调控这种组织或细胞类型特异性表达的启动子元件,我们构建了各种AldP启动子-β-葡萄糖醛酸酶(GUS)融合基因,并将它们转入烟草植株。对转基因烟草中GUS活性的分析表明,在2.0 kb的AldP启动子区域内至少存在两个元件。一个位于从-2.0 kb到-1.2 kb的片段内,起负调控元件的作用。另一个是位于-1.2 kb和-0.31 kb之间的正调控元件,赋予发育调控的叶肉细胞特异性表达。此外,转录起始位点两侧的1.2 kb水稻启动子片段包含一个作为烟草光诱导靶点的元件。结果表明,单子叶植物水稻的AldP基因启动子能在双子叶植物烟草中以基本的生理方式发挥作用。