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大肠杆菌中钝性DNA末端与3'突出单链的连接。

The joining of blunt DNA ends to 3'-protruding single strands in Escherichia coli.

作者信息

King J, Fairley C, Morgan W

机构信息

Department of Radiation Oncology, University of California, San Francisco, San Francisco, CA 94143-0750, USA.

出版信息

Nucleic Acids Res. 1998 Apr 1;26(7):1749-54. doi: 10.1093/nar/26.7.1749.

Abstract

In eukaryotic and prokaryotic organisms DNA double-strand breaks with non-complementary ends can be joined by mechanisms of illegitimate recombination. We examined the joining of 3'-protruding single strand (PSS) ends, which do not have recessed 3' hydroxyls that can allow for fill-in DNA synthesis, to blunt ends. End-joining was examined by electro-transforming Escherichia coli strains with linearized plasmid DNA, sequencing the resulting junctions, and determining the transformation frequencies. Three different E.coli strains were examined: MC1061, which has no known recombination or DNA repair defects, HB101 (rec A-) and SURE (recB- recJ-). No striking differences were found in either the spectrum of products observed or the efficiency of end-joining between these strains. As in vertebrate systems, the majority of the products were overlaps between directly repeated DNA sequences. 3'-PSS are frequently preserved in vertebrate systems, but they were not preserved in our experiments unless the transforming DNA was pretreated with a DNA polymerase.

摘要

在真核生物和原核生物中,具有非互补末端的DNA双链断裂可通过异常重组机制连接。我们研究了3'突出单链(PSS)末端与平端的连接,3'突出单链末端没有可用于填补DNA合成的凹陷3'羟基。通过用线性化质粒DNA电转化大肠杆菌菌株、对所得连接点进行测序并确定转化频率来检测末端连接。检测了三种不同的大肠杆菌菌株:没有已知重组或DNA修复缺陷的MC1061、HB101(rec A-)和SURE(recB- recJ-)。在这些菌株之间观察到的产物谱或末端连接效率方面均未发现显著差异。与脊椎动物系统一样,大多数产物是直接重复DNA序列之间的重叠。3'-PSS在脊椎动物系统中经常保留,但在我们的实验中,除非用DNA聚合酶对转化DNA进行预处理,否则它们不会保留。

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