Sasaki Yuko, Ishikawa Jun, Yamashita Atsushi, Oshima Kenshiro, Kenri Tsuyoshi, Furuya Keiko, Yoshino Chie, Horino Atsuko, Shiba Tadayoshi, Sasaki Tsuguo, Hattori Masahira
Department of Bacterial Pathogenesis and Infection Control, National Institute of Infectious Diseases, 4-7-1, Gakuen, Musashimurayama, Tokyo, Japan.
Nucleic Acids Res. 2002 Dec 1;30(23):5293-300. doi: 10.1093/nar/gkf667.
The complete genomic sequence of an intracellular bacterial pathogen, Mycoplasma penetrans HF-2 strain, was determined. The HF-2 genome consists of a 1 358 633 bp single circular chromosome containing 1038 predicted coding sequences (CDSs), one set of rRNA genes and 30 tRNA genes. Among the 1038 CDSs, 264 predicted proteins are common to the Mycoplasmataceae sequenced thus far and 463 are M.penetrans specific. The genome contains the two-component system but lacks the essential cellular gene, uridine kinase. The relatively large genome of M.penetrans HF-2 among mycoplasma species may be accounted for by both its rich core proteome and the presence of a number of paralog families corresponding to 25.4% of all CDSs. The largest paralog family is the p35 family, which encodes surface lipoproteins including the major antigen, P35. A total of 44 genes for p35 and p35 homologs were identified and 30 of them form one large cluster in the chromosome. The genetic tree of p35 paralogs suggests the occurrence of dynamic chromosomal rearrangement in paralog formation during evolution. Thus, M.penetrans HF-2 may have acquired diverse repertoires of antigenic variation-related genes to allow its persistent infection in humans.
确定了一种细胞内细菌病原体——穿透支原体HF-2菌株的完整基因组序列。HF-2基因组由一条1358633 bp的单环染色体组成,包含1038个预测的编码序列(CDS)、一组rRNA基因和30个tRNA基因。在这1038个CDS中,264个预测的蛋白质是迄今为止已测序的支原体科共有的,463个是穿透支原体特有的。该基因组包含双组分系统,但缺乏必需的细胞基因尿苷激酶。穿透支原体HF-2在支原体物种中相对较大的基因组可能是由于其丰富的核心蛋白质组以及对应于所有CDS的25.4%的多个旁系同源家族的存在。最大的旁系同源家族是p35家族,它编码包括主要抗原P35在内的表面脂蛋白。总共鉴定出44个p35和p35同源物的基因,其中30个在染色体上形成一个大簇。p35旁系同源物的遗传树表明在进化过程中旁系同源物形成过程中发生了动态染色体重排。因此,穿透支原体HF-2可能获得了与抗原变异相关的多种基因库,以使其能够在人类中持续感染。