Herzer P J, Inouye S, Inouye M
Department of Biochemistry, Robert Wood Johnson Medical School, University of Medicine and Dentistry of New Jersey, Rutgers, Piscataway 08854.
Mol Microbiol. 1992 Feb;6(3):345-54. doi: 10.1111/j.1365-2958.1992.tb01477.x.
Some natural isolates of Escherichia coli have been shown to produce a unique branched RNA-linked single-stranded DNA called msDNA. These bacteria contain a retro-element called retron consisting of the msr-msd region and the gene for reverse transcriptase (RT). All three E. coli retrons characterized to date have been shown to be integrated into a prophage or to be associated with phage-related genes. In this report, we identified a new msDNA from an E. coli wild strain. Using the msDNA as a probe, the retron for the msDNA was cloned and its DNA sequence was determined. The retron was found to consist of a 1.3kb DNA fragment, making it the smallest retron isolated to date. The msDNA produced from the retron consists of a 107 base single-stranded DNA, which is considered to be branched out from the 18th G residue of a 75-base RNA molecule by a 2',5'-phosphodiester linkage. Thus, the msDNA and the retron were designated msDNA-Ec107 and retron-Ec107, respectively. Most significantly, retron-Ec107 was inserted into the E. coli genome by replacing a 34bp intergenic sequence between the pyrE and ttk genes located at 82 min on the E. coli chromosome. Interestingly, the retron contains palindromic structures at both ends and the E. coli 34bp intergenic sequence also contains a 10bp inverted repeat structure. These palindromic structures might have played a role in the integration of retron-Ec107 into the E. coli genome.
一些大肠杆菌的天然分离株已被证明能产生一种独特的、与RNA相连的单链DNA,称为多顺反子msDNA。这些细菌含有一种称为反转录子的反转录元件,它由msr-msd区域和逆转录酶(RT)基因组成。迄今为止,已鉴定出的所有三种大肠杆菌反转录子都被证明整合到了原噬菌体中,或与噬菌体相关基因有关。在本报告中,我们从一株大肠杆菌野生菌株中鉴定出一种新的msDNA。以该msDNA为探针,克隆了其反转录子并测定了DNA序列。发现该反转录子由一个1.3kb的DNA片段组成,是迄今为止分离出的最小的反转录子。该反转录子产生的msDNA由107个碱基的单链DNA组成,它被认为通过2',5'-磷酸二酯键从一个75个碱基的RNA分子的第18个G残基处分支出来。因此,该msDNA和反转录子分别被命名为msDNA-Ec107和retron-Ec107。最显著的是,retron-Ec107通过取代位于大肠杆菌染色体82分钟处的pyrE和ttk基因之间的一段34bp基因间序列插入到大肠杆菌基因组中。有趣的是,该反转录子两端都含有回文结构,大肠杆菌的34bp基因间序列也含有一个10bp的反向重复结构。这些回文结构可能在retron-Ec107整合到大肠杆菌基因组中发挥了作用。