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转座元件IS1中的碱基替换会导致质粒共整合靶位点处出现长度可变的DNA重复。

Base substitutions in transposable element IS1 cause DNA duplication of variable length at the target site for plasmid co-integration.

作者信息

Machida C, Machida Y

出版信息

EMBO J. 1987 Jun;6(6):1799-803. doi: 10.1002/j.1460-2075.1987.tb02433.x.

Abstract

We demonstrate that base substitutions in the IS1 sequence affect the length of the nucleotide sequence which is duplicated during IS1-mediated co-integration. IS1K, an IS1 variant present in the Escherichia coli chromosome, has seven base substitutions in its sequence as compared with that of IS1R derived from the plasmid R100. All substitutions are located in the internal region of IS1K. We have constructed plasmids containing IS1R, IS1K and hybrids between them: one contains four base substitutions causing an amino acid substitution in the insA gene and the other has three substitutions producing an amino acid substitution in the insB gene. We have isolated co-integrate plasmids formed by each IS1 and analysed nucleotide sequences of the target sites duplicated at the co-integration junctions. The results show that IS1K generates duplications of 8 or 14 bp as well as 9 bp, while IS1R exclusively generates the 9-bp duplications. Both hybrid IS1s also create 8- or 7-bp target duplications in addition to 9-bp duplications. These results indicate that the base substitutions in either insA or insB are sufficient for the occurrence of unusual target duplications, suggesting that both genes are involved in the target duplication.

摘要

我们证明,IS1序列中的碱基替换会影响在IS1介导的共整合过程中被复制的核苷酸序列的长度。IS1K是存在于大肠杆菌染色体中的一种IS1变体,与源自质粒R100的IS1R相比,其序列中有七个碱基替换。所有替换都位于IS1K的内部区域。我们构建了含有IS1R、IS1K及其之间杂种的质粒:一个含有四个碱基替换,导致insA基因中的氨基酸替换,另一个有三个替换,在insB基因中产生氨基酸替换。我们分离了由每个IS1形成的共整合质粒,并分析了在共整合连接处复制的靶位点的核苷酸序列。结果表明,IS1K产生8或14 bp以及9 bp的重复,而IS1R仅产生9 bp的重复。两种杂种IS1除了产生9 bp的重复外,还产生8或7 bp的靶重复。这些结果表明,insA或insB中的碱基替换足以导致异常靶重复的出现,这表明这两个基因都参与了靶重复。

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Transposable elements in prokaryotes.原核生物中的转座元件。
Annu Rev Genet. 1981;15:341-404. doi: 10.1146/annurev.ge.15.120181.002013.
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