Old I G, Margarita D, Saint Girons I
Unité de Bactériologie Moléculaire et Médicale, Institut Pasteur, Paris, France.
FEMS Microbiol Lett. 1993 Jul 15;111(1):109-14. doi: 10.1111/j.1574-6968.1993.tb06369.x.
The complete nucleotide sequence of the Borrelia burgdorferi dnaA gene (encoding the initiator protein of chromosome replication) and its flanking regions was determined. The putative DnaA polypeptide exhibited 29-42% identity with those of other eubacteria. The gene order in the dnaA region at the centre of the B. burgdorferi linear chromosome is rnpA-rpmH-dnaN-dnaA-gyrB-gyrA in contrast to the consensus eubacterial order of rnpA-rpmH-dnaA-dnaN-recF-gyrB, suggesting a rearrangement during the evolution of the Borrelia chromosome. We did not detect the multiple 9-nucleotide repeats known as DnaA boxes, which characterise origin of replications, in the dnaA-gyrB and dnaA-dnaN intergenic regions. In addition B. burgdorferi DnaA protein differs considerably from those of other eubacteria in a normally highly conserved region at the C-terminus of the polypeptide which may be involved in DNA binding.
测定了伯氏疏螺旋体dnaA基因(编码染色体复制起始蛋白)及其侧翼区域的完整核苷酸序列。推测的DnaA多肽与其他真细菌的DnaA多肽有29%-42%的同源性。与真细菌一致的rnpA-rpmH-dnaA-dnaN-recF-gyrB基因顺序不同,伯氏疏螺旋体线性染色体中心的dnaA区域的基因顺序是rnpA-rpmH-dnaN-dnaA-gyrB-gyrA,这表明在疏螺旋体染色体进化过程中发生了重排。我们在dnaA-gyrB和dnaA-dnaN基因间区域未检测到作为复制起点特征的多个9核苷酸重复序列,即DnaA框。此外,伯氏疏螺旋体DnaA蛋白在多肽C末端一个通常高度保守的区域与其他真细菌的DnaA蛋白有很大差异,该区域可能参与DNA结合。