Department of Botany, University of Durham, South Road, DH1 3LE, Durham, UK.
Plant Mol Biol. 1988 May;10(3):203-14. doi: 10.1007/BF00027397.
A 3.4-kilobase genomic DNA fragment from Pisum sativum L. containing the LegA gene, which encodes a major legumin storage protein, was transferred to Nicotiana plumbaginifolia using an Agrobacterium tumefaciens strain containing the Bin 19 binary vector system. Northern hybridisation analysis of legA-transformed plants demonstrated that legumin-specific RNA was present in developing seeds but not in developing leaves. Legumin protein was immunologically detected in the mature seeds of legA-transformed plants, and was present as the correct-size protein composed of disulphide-bonded polypeptides. It is concluded that the transferred pea genomic fragment contains all the information necessary for seed-specific expression of the legA gene, and for correct processing of the primary transcript and the precursor legumin protein.
豌豆基因组中含有 LegA 基因的 3.4 千碱基对 DNA 片段,该基因编码一种主要的豆球蛋白贮藏蛋白。使用含有 Bin 19 二元载体系统的根癌农杆菌菌株将该基因转移到烟草属植物中。对 LegA 转化植物的 Northern 杂交分析表明,豆球蛋白特异性 RNA 存在于发育中的种子中,但不存在于发育中的叶片中。在 LegA 转化植物的成熟种子中,免疫检测到豆球蛋白蛋白,并且存在由二硫键连接的多肽组成的正确大小的蛋白。因此,可以得出结论,转移的豌豆基因组片段包含 LegA 基因在种子中特异性表达以及正确加工初级转录物和前体豆球蛋白蛋白所需的所有信息。