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珠蛋白基因的体外酶促合成

Enzymatic in vitro synthesis of globin genes.

作者信息

Efstratiadis A, Kafatos F C, Maxam A M, Maniatis T

出版信息

Cell. 1976 Feb;7(2):279-88. doi: 10.1016/0092-8674(76)90027-1.

Abstract

Full-length, single-stranded rabbit globin cDNA, synthesized by AMV reverse transcriptase, apparently contains a small double-stranded sequence (hairpin) at the 3' terminus. This cDNA can serve as template-primer for E. coli DNA polymerase I, which synthesizes a strand complementary to the cDNA and covalently bound to it. The loop connecting the two strands can be cut by S1 nuclease. Reassociation, hybridization, and restriction endonuclease studies, as well as electrophoretic analyses, indicate that the sequential actions of reverse transcriptase, DNA polymerase 1, and S1 nuclease generate full-length, double-stranded synthetic globin genes.

摘要

由禽成髓细胞瘤病毒逆转录酶合成的全长单链兔珠蛋白cDNA,在3'末端显然含有一小段双链序列(发夹结构)。这种cDNA可作为大肠杆菌DNA聚合酶I的模板引物,该酶能合成与cDNA互补并与之共价结合的一条链。连接两条链的环可被S1核酸酶切割。重缔合、杂交、限制性内切酶研究以及电泳分析表明,逆转录酶、DNA聚合酶I和S1核酸酶的相继作用产生了全长双链合成珠蛋白基因。

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