Holk A, Kaldenhoff R, Richter G
Institut für Botanik, Universität Hannover, Germany.
Plant Mol Biol. 1996 Sep;31(6):1153-61. doi: 10.1007/BF00040832.
According to previous studies the expression of the gene DC 2.15 is induced in cultured carrot cells after a transfer to an auxin-free medium, where somatic embryo development occurs. This embryogenic gene encodes a prolinerich protein, which resembles proteins involved in auxin-controlled developmental processes. To understand the mechanism underlying the regulation of DC 2.15, an experimental approach has been employed which allows the direct identification of the DC 2.15 promoter structure by applying PCR techniques. We demonstrate the presence of five distinct promoter sequences highly similar in structure, but slightly different in a common region of about 15 nucleotides, which contain the binding site for the GATA factor originally found in the human HOX gene. Activity of each promoter structure was assessed in developing somatic embryos containing the specific sequence fused to the beta-glucuronidase (GUS) reporter gene. For two of the five promoter structures a drastic increase in activity was registered during the torpedo stage while the remaining three were inactive throughout the stages of somatic embryogenesis.
根据先前的研究,基因DC 2.15在转移至无生长素培养基后,在培养的胡萝卜细胞中被诱导表达,体细胞胚胎发育在此培养基中发生。这个胚胎发生基因编码一种富含脯氨酸的蛋白质,它类似于参与生长素控制的发育过程的蛋白质。为了理解DC 2.15调控的潜在机制,采用了一种实验方法,该方法通过应用PCR技术直接鉴定DC 2.15启动子结构。我们证明存在五个不同的启动子序列,它们在结构上高度相似,但在大约15个核苷酸的共同区域略有不同,该区域包含最初在人类HOX基因中发现的GATA因子的结合位点。在含有与β-葡萄糖醛酸酶(GUS)报告基因融合的特定序列的发育中的体细胞胚胎中评估每个启动子结构的活性。在五个启动子结构中的两个中,在鱼雷期观察到活性急剧增加,而其余三个在体细胞胚胎发生的各个阶段均无活性。