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机构地区:[1]中国农业科学院生物技术研究中心 [2]北京大学生命科学院生物化学与分子生物学系
出 处:《中国生物化学与分子生物学报》1998年第6期668-672,共5页Chinese Journal of Biochemistry and Molecular Biology
基 金:863计划项目
摘 要:利用逆转录-聚合酶链式反应(RT-PCR)方法从玉米掖单-20开花后10d的叶片中分离到21kD玉米种子贮存蛋白cDNA(N21KZY),并进行了序列分析.其编码蛋白包含211个氨基酸,极其富含甲硫氨酸,高达27%;其N端有一个21个氨基酸的信号肽.N21KZY及其编码蛋白和Chui等人分离的该基因的基因组克隆及其编码蛋白的同源性分别为95.1%和90.5%;两者的编码蛋白与玉米10kD醇溶蛋白极其相似,其中间多出一个54氨基酸的肽段和一个6氨基酸的肽段,这表明它们可能是来源于同一个祖先基因,后来通过基因重排、缺失或不均等交换等过程而形成的不同的蛋白质.A total RNA of maize Yedan 20 was extracted from the leaves 10 days after flowering,and a cDNA was obtained from reverse transcript solution of total RNA and a pair of Oligo dT primer.Then,a 21 kD cDNA was isolated from RT PCR products by using a pair of the specific primers.Having recovered from an agarose gel,the specific 21 kD cDNA (N21KZY) was treated and cloned into a pBluescript (KS +) vector.Through screening the blue white colonies,the 21 kD gene was sequenced and characterized.The sequencing result of the 21 kD gene showsed the N21KZY encoded a protein of 211 amino acids,exceptionally rich in methionine up to 27% proportion,with a signal peptide of 21 amino acids in its N terminus.DNA sequence of N21KZY and its encoding protein shared 95 1%,90 5% homology with those of N21KC isolated by Chui et al.Both of their encoding proteins were identical to 10 kD zein,with an extra domain of 54 amino acids and a peptide of 6 amino acids probably caused by gene rearrangement,deletion,non equational interchange or other events of their common ancestor gene.
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