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编码酵母丙氨酸tRNA两个半分子的DNA的克隆
引用本文:刘建华,王德宝.编码酵母丙氨酸tRNA两个半分子的DNA的克隆[J].中国生物化学与分子生物学报,1992,8(4):488-491.
作者姓名:刘建华  王德宝
作者单位:中国科学院上海生物化学研究所分子生物学国家重点实验室,中国科学院上海生物化学研究所分子生物学国家重点实验室 上海 200031,上海 200031
摘    要:用DNA合成仪合成寡聚脱氧核苷酸。用T4-DNA连接酶把这些寡聚脱氧核苷酸重组成双链DNA。这两个双链DNA的上游是T7-启动子,下游分别编码酵母丙氨酸tRNA的5′半分子(1-35位核苷酸)和3′半分子(35-76位核苷酸)。再把这两个双链DNA克隆到PUC 12质粒中。经点杂交筛选和DNA顺序测定证明克隆是成功的。

关 键 词:DNA化学合成  DNA克隆  酵母丙氨酸tRNA  
收稿时间:1992-08-20

Cloning of DNAs Coding for the Two Half Molecules of Yeast Alanine tRNA
Liu,Jian-hua Wang,De-bao.Cloning of DNAs Coding for the Two Half Molecules of Yeast Alanine tRNA[J].Chinese Journal of Biochemistry and Molecular Biology,1992,8(4):488-491.
Authors:Liu  Jian-hua Wang  De-bao
Institution:(T.P.Wang)(Shanghai Molecular Biology Laboratory,Shanghai Institute of Biochemistry,Academia Sinica 200031
Abstract:Six oligodeoxynucleotides were synthesized on a DNA synthesizer.These fragments were constructed into two DNA double strands with T4-DNA ligase.The upstream sequences of both double strands were T7-promoter, and their downstream sequences were coding for the 5'-half molecule (1-35 nucleotides) and the 3'-half molecule (35-76 nucleotides) of yeast alanine tRNA repectively.These double strands were cloned into a plamid PUC 12.The successful cloning was confirmed by site hybrid screening and DNA sequencing.
Keywords:Chemical synthesis of DNA  DNA cloning  Yeast alanine tRNA
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