Dunn J J, Buchstein S R, Butler L L, Fisenne S, Polin D S, Lade B N, Luft B J
Biology Department, Brookhaven National Laboratory, Upton, New York 11973-5000.
J Bacteriol. 1994 May;176(9):2706-17. doi: 10.1128/jb.176.9.2706-2717.1994.
We have determined the complete nucleotide sequence of a small circular plasmid from the spirochete Borrelia burgdorferi Ip21, the agent of Lyme disease. The plasmid (cp8.3/Ip21) is 8,303 bp long, has a 76.6% A+T content, and is unstable upon passage of cells in vitro. An analysis of the sequence revealed the presence of two nearly perfect copies of a 184-bp inverted repeat sequence separated by 2,675 bp containing three closely spaced, but nonoverlapping, open reading frames (ORFs). Each inverted repeat ends in sequences that may function as signals for the initiation of transcription and translation of flanking plasmid sequences. A unique oligonucleotide probe based on the repeated sequence showed that the DNA between the repeats is present predominantly in a single orientation. Additional copies of the repeat were not detected elsewhere in the Ip21 genome. An analysis for potential ORFs indicates that the plasmid has nine highly probable protein-coding ORFs and one that is less probable; together, they occupy almost 71% of the nucleotide sequence. Analysis of the deduced amino acid sequences of the ORFs revealed one (ORF-9) with features in common with Borrelia lipoproteins and another (ORF-2) having limited homology with a replication protein, RepC, from a gram-positive plasmid that replicates by a rolling circle (RC) mechanism. Known collectively as RC plasmids, such plasmids require a double-stranded origin at which the Rep protein nicks the DNA to generate a single-stranded replication intermediate. cp8.3/Ip21 has three copies of the heptameric motif characteristically found at a nick site of most RC plasmids. These observations suggest that cp8.3/Ip21 may replicate by an RC mechanism.
我们已经确定了来自莱姆病病原体——螺旋体伯氏疏螺旋体Ip21的一个小环形质粒的完整核苷酸序列。该质粒(cp8.3/Ip21)长8303 bp,A+T含量为76.6%,在体外细胞传代时不稳定。序列分析显示存在两个近乎完美的184 bp反向重复序列拷贝,它们被2675 bp隔开,其中包含三个紧密间隔但不重叠的开放阅读框(ORF)。每个反向重复序列的末端序列可能作为侧翼质粒序列转录和翻译起始的信号。基于重复序列的独特寡核苷酸探针表明,重复序列之间的DNA主要以单一方向存在。在Ip21基因组的其他地方未检测到重复序列的额外拷贝。对潜在ORF的分析表明,该质粒有九个高度可能的蛋白质编码ORF和一个可能性较小的;它们总共占据了近71%的核苷酸序列。对ORF推导的氨基酸序列分析显示,一个(ORF-9)具有与伯氏疏螺旋体脂蛋白共同的特征,另一个(ORF-2)与来自通过滚环(RC)机制复制的革兰氏阳性质粒的复制蛋白RepC具有有限的同源性。这类质粒统称为RC质粒,它们需要一个双链起点,Rep蛋白在该起点处切割DNA以产生单链复制中间体。cp8.3/Ip21具有大多数RC质粒切口位点特有的七聚体基序的三个拷贝。这些观察结果表明cp8.3/Ip21可能通过RC机制复制。