首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Retron for the 67-base multicopy single-stranded DNA from Escherichia coli: a potential transposable element encoding both reverse transcriptase and Dam methylase functions.
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Retron for the 67-base multicopy single-stranded DNA from Escherichia coli: a potential transposable element encoding both reverse transcriptase and Dam methylase functions.

机译:从大肠杆菌的67碱基多拷贝单链DNA反转录:编码逆转录酶和Dam甲基化酶功能的潜在转座因子。

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摘要

The region (retron-Ec67) required for the biosynthesis of a branched-RNA-linked multicopy single-stranded DNA (msDNA-Ec67) from a clinical isolate of Escherichia coli was mapped at a position equivalent to 19 min on the K-12 chromosome. The element containing the retron consisted of a unique 34-kilobase sequence that was flanked by direct repeats of a 26-base-pair sequence found in the K-12 chromosomal DNA. This suggests that the 34-kilobase element was probably integrated into the E. coli genome by a mechanism related to transposition or phage integration. In the 34-kilobase sequence an open reading frame of 285 residues was found, which displays 44% sequence identity with the E. coli Dam methylase. Interestingly, there are three GATC sequences, the site of Dam methylation, in the promoter region of the gene for reverse transcriptase.
机译:从大肠杆菌的临床分离物中生物合成支链RNA连接的多拷贝单链DNA(msDNA-Ec67)所需的区域(retron-Ec67)被定位在K-12染色体上相当于19分钟的位置。包含补体的元件由独特的34碱基碱基序列组成,该序列的两侧是在K-12染色体DNA中发现的26个碱基对序列的直接重复。这表明34-碱基碱基的元件可能是通过与转座或噬菌体整合有关的机制整合到大肠杆菌基因组中的。在34碱基对的序列中,发现一个285个残基的开放阅读框,与大肠杆菌Dam甲基化酶显示44%的序列同一性。有趣的是,在逆转录酶基因的启动子区域中存在三个GATC序列,即Dam甲基化位点。

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