Kim K, Jeong D, Lim D
Department of Microbiology, Gyeongsang National University, Gazwadong, Chinju, Korea.
J Bacteriol. 1997 Oct;179(20):6518-21. doi: 10.1128/jb.179.20.6518-6521.1997.
Multicopy single-stranded DNA (msDNA) molecules consist of single-stranded DNA covalently linked to RNA. Such molecules are encoded by genetic elements called retrons. Unlike other retrons, retron EC83 isolated from Escherichia coli 161 produces RNA-free msDNA by site-specific cleavage of msDNA at 5'-TTGA/A-3', where the slash indicates the cleavage site. In order to investigate factors responsible for the msDNA cleavage, retron EC83 was treated with hydroxylamine and colonies were screened for cleavage-negative mutants. We isolated three mutants which were defective in msDNA cleavage and produced RNA-linked msDNA. They were all affected in msd, a gene for msDNA, with a base substitution at the bottom part of the msDNA stem. In contrast, base substitution at and around the cleavage site has no marked effect on msDNA synthesis or its cleavage. From these results, we concluded that the nucleotides at the bottom of the msDNA stem, but not the nucleotides at the cleavage site, play a major role in the recognition and cleavage of msDNA EC83.
多拷贝单链DNA(msDNA)分子由与RNA共价连接的单链DNA组成。此类分子由称为反转录子的遗传元件编码。与其他反转录子不同,从大肠杆菌161中分离出的反转录子EC83通过在5'-TTGA/A-3'处对msDNA进行位点特异性切割产生不含RNA的msDNA,其中斜线表示切割位点。为了研究负责msDNA切割的因素,用羟胺处理反转录子EC83,并筛选菌落以寻找切割阴性突变体。我们分离出三个在msDNA切割方面有缺陷并产生与RNA相连的msDNA的突变体。它们在msd(一个与msDNA相关的基因)中均受到影响,msDNA茎底部有一个碱基替换。相比之下,切割位点及其周围的碱基替换对msDNA合成或其切割没有明显影响。根据这些结果,我们得出结论,msDNA茎底部的核苷酸而非切割位点的核苷酸在msDNA EC83的识别和切割中起主要作用。