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外源导入原生质体的水稻半胱氨酸蛋白酶抑制剂及转基因水稻的再生

Oryzacystatin exogenously introduced into protoplasts and regeneration of transgenic rice.

作者信息

Hosoyama H, Irie K, Abe K, Arai S

机构信息

Department of Agricultural Chemistry, Faculty of Agriculture, University of Tokyo, Japan.

出版信息

Biosci Biotechnol Biochem. 1994 Aug;58(8):1500-5. doi: 10.1271/bbb.58.1500.

Abstract

Oryzacystatin (OC) is a proteinaceous cysteine proteinase inhibitor involved in the biodefense of rice seeds. To create transgenic rice plants with increased OC activity, we introduced an OC expressing vector into rice protoplasts and obtained transformed calli. The expression vector contained a bacterial inaA DNA fragment in the 3'-noncoding region as a tag to distinguish the introduced DNA from the intrinsic OC gene. The OC vector and a selection marker gene conferring hygromycin resistance were used together to transfect into rice protoplasts. A number of hygromycin-resistant calli were obtained and studied by polymerase chain reaction and genomic Southern blotting to find if the exogenous OC gene had been integrated. The calli were studied by northern blotting as well to examine mRNA expression. The results showed that integration and expression of the introduced OC gene occurred in 51% and 27%, respectively, of 156 subcultures from 15 hygromycin-resistant calli. As a final step, transgenic rice plants were regenerated from the calli expressing OC. Leaves and seeds from the plants had higher OC activities than those from nontransgenic plants.

摘要

水稻半胱氨酸蛋白酶抑制剂(OC)是一种参与水稻种子生物防御的蛋白质类半胱氨酸蛋白酶抑制剂。为了培育具有更高OC活性的转基因水稻植株,我们将一个OC表达载体导入水稻原生质体并获得了转化愈伤组织。该表达载体在3'-非编码区含有一个细菌inaA DNA片段作为标签,以区分导入的DNA与内源OC基因。将OC载体和一个赋予潮霉素抗性的选择标记基因一起用于转染水稻原生质体。获得了许多潮霉素抗性愈伤组织,并通过聚合酶链反应和基因组Southern杂交进行研究,以确定外源OC基因是否已整合。还通过Northern杂交对愈伤组织进行研究,以检测mRNA表达。结果表明,在来自15个潮霉素抗性愈伤组织的156次继代培养中,导入的OC基因的整合率和表达率分别为51%和27%。作为最后一步,从表达OC的愈伤组织中再生出转基因水稻植株。这些植株的叶片和种子的OC活性高于非转基因植株。

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