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大肠杆菌K-12中由小鼠H-2基因序列构成的复杂异源双链体的校正

Correction of complex heteroduplexes made of mouse H-2 gene sequences in Escherichia coli K-12.

作者信息

Cami B, Chambon P, Kourilsky P

出版信息

Proc Natl Acad Sci U S A. 1984 Jan;81(2):503-7. doi: 10.1073/pnas.81.2.503.

Abstract

We have prepared heteroduplexes between two plasmids that carry, in the same orientation, two H-2 cDNA inserts, 1.15 and 1.0 kilobase long, respectively. Their sequences encode two distinct class I transplantation antigens of the mouse and differ by 8% of their nucleotides. Molecules with a rearranged array of restriction sites were found after transformation and cloning in an Escherichia coli recA- host. Nucleotide sequences showed that the rearranged molecules derived their nucleotides from the two parental strands. Thus, correction of these complex heteroduplexes takes place in E. coli and probably involves repair mechanisms. It provides the basis for a mutational process in which several nucleotides (amino acids) can be altered in a single event. It also offers a practical means of making genetic variants. Several other implications are discussed.

摘要

我们制备了两个质粒之间的异源双链体,这两个质粒以相同方向携带两个H-2 cDNA插入片段,分别长1.15千碱基和1.0千碱基。它们的序列编码小鼠的两种不同的I类移植抗原,核苷酸序列有8%的差异。在转化并克隆到大肠杆菌recA-宿主中后,发现了具有重排限制酶切位点阵列的分子。核苷酸序列表明,重排分子的核苷酸来自两条亲代链。因此,这些复杂异源双链体的校正发生在大肠杆菌中,可能涉及修复机制。它为一种突变过程提供了基础,在这个过程中几个核苷酸(氨基酸)可以在单个事件中被改变。它还提供了一种产生遗传变体的实用方法。文中还讨论了其他几个影响。

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