Kausch A P, Owen T P, Zachwieja S J, Flynn A R, Sheen J
University of Rhode Island, Department of Plant Science, Kingston 02892, USA.
Plant Mol Biol. 2001 Jan;45(1):1-15. doi: 10.1023/a:1006487326533.
To play an essential role in C4 photosynthesis, the maize C4 phosphoenolpyruvate carboxylase gene (PPCZm1) acquired many new expression features, such as leaf specificity, mesophyll specificity, light inducibility and high activity, that distinguish the unique C4 PPC from numerous non-C4 PPC genes in maize. We present here the first investigation of the developmental, cell-specific, light and metabolic regulation of the homologous C4 PPCZm1 promoter in stable transgenic maize plants. We demonstrate that the 1.7 kb of the 5'-flanking region of the PPCZm1 gene is sufficient to direct the C4-specific expression patterns of beta-glucuronidase (GUS) activity, as a reporter, in stable transformed maize plants. In light-grown shoots, GUS expression was strongest in all developing and mature mesophyll cells in the leaf, collar and sheath. GUS activity was also detected in mesophyll cells in the outer husks of ear shoots and in the outer glumes of staminate spikelets. We did not observe histological localization of GUS activity in light- or dark-grown callus, roots, silk, developing or mature kernels, the shoot apex, prop roots, or pollen. In addition, we used the stable expressing transformants to conduct and quantify physiological induction studies. Our results indicate that the expression of the C4 PPCZm1-GUS fusion gene is mesophyll-specific and influenced by development, light, glucose, acetate and chloroplast biogenesis in transgenic maize plants. These studies suggest that the adoption of DNA regulatory elements for C4-specific gene expression is a crucial step in C4 gene evolution.
为了在C4光合作用中发挥重要作用,玉米C4磷酸烯醇式丙酮酸羧化酶基因(PPCZm1)获得了许多新的表达特征,如叶片特异性、叶肉特异性、光诱导性和高活性,这些特征将独特的C4型磷酸烯醇式丙酮酸羧化酶与玉米中众多非C4型磷酸烯醇式丙酮酸羧化酶基因区分开来。我们在此首次对稳定转基因玉米植株中同源C4 PPCZm1启动子的发育、细胞特异性、光和代谢调控进行了研究。我们证明,PPCZm1基因5'侧翼区域的1.7 kb足以在稳定转化的玉米植株中指导作为报告基因的β-葡萄糖醛酸酶(GUS)活性的C4特异性表达模式。在光照生长的芽中,GUS表达在叶片、叶环和叶鞘中所有发育中的和成熟的叶肉细胞中最强。在雌穗芽的外颖壳和雄小穗的外稃的叶肉细胞中也检测到了GUS活性。我们在光照或黑暗培养的愈伤组织、根、花丝、发育中的或成熟的籽粒、茎尖、支柱根或花粉中未观察到GUS活性的组织学定位。此外,我们使用稳定表达的转化体进行并定量生理诱导研究。我们的结果表明,C4 PPCZm1-GUS融合基因的表达在转基因玉米植株中是叶肉特异性的,并且受发育、光、葡萄糖、乙酸盐和叶绿体生物发生的影响。这些研究表明,采用用于C4特异性基因表达的DNA调控元件是C4基因进化中的关键一步。