Shirsat A H, Meakin P J, Gatehouse J A
Department of Biological Sciences, University of Durham, UK.
Plant Mol Biol. 1990 Nov;15(5):685-93. doi: 10.1007/BF00016119.
The function of the 28 bp conserved Leg box element found in the 11S legumin-like genes of Vicia, Pisum, Glycine and Helianthus in controlling gene expression has been examined. Transgenic tobacco plants containing 124 bp of 5' legA flanking sequence including the Leg box and all sequences downstream to the start of transcription failed to activate the gene, as judged by ELISA and northern assays. Expression was first detected in a promoter truncation construct which contained 549 bp of 5' flanking sequence. These two promoter truncation constructs were additionally examined for their ability to interact with pea seed nuclear proteins. The use of DNA-protein binding and mobility shift assays showed that the -124 bp fragment which included the Leg box did not bind nuclear proteins. In contrast, nuclear proteins were shown to strongly bind to the -549 bp flanking sequence fragment. The correlation of transgenic plant analysis with DNA binding assays indicates that the highly conserved 28 bp Leg box element is not the sole promoter determinant in legumin gene expression.
已对在蚕豆、豌豆、大豆和向日葵的11S豆球蛋白样基因中发现的28bp保守Leg盒元件在控制基因表达方面的功能进行了研究。通过ELISA和Northern分析判断,含有包括Leg盒在内的124bp 5' legA侧翼序列以及转录起始点下游所有序列的转基因烟草植株未能激活该基因。在含有549bp 5' 侧翼序列的启动子截短构建体中首次检测到表达。还对这两个启动子截短构建体与豌豆种子核蛋白相互作用的能力进行了检测。DNA-蛋白质结合和迁移率变动分析表明,包含Leg盒的-124bp片段不与核蛋白结合。相反,核蛋白被证明能与-549bp侧翼序列片段强烈结合。转基因植物分析与DNA结合分析的相关性表明,高度保守的28bp Leg盒元件不是豆球蛋白基因表达中唯一的启动子决定因素。