Ladefoged S A, Christiansen G
Institute of Medical Microbiology, University of Aarhus, Denmark.
J Bacteriol. 1992 Apr;174(7):2199-207. doi: 10.1128/jb.174.7.2199-2207.1992.
We present the complete maps of five Mycoplasma hominis genomes, including a detailed restriction map and the locations of a number of genetic loci. The restriction fragments were resolved by field inversion gel electrophoresis or by the contour-clamped homogeneous-electric-field system of pulsed-field gel electrophoresis. All the ApaI, SmaI, BamHI, XhoI, and SalI restriction sites (total of 21 to 33 sites in each strain) were placed on the physical map, yielding an average resolution of 26 kb. The maps were constructed using three different approaches: (i) size determination of DNA fragments partially or completely cleaved with one or two restriction enzymes, (ii) hybridization analysis with purified restriction fragments and specific probes, and (iii) use of linking clones. A genetic map was constructed by hybridization with gene-specific probes for rpoA, rpoC, rrn, tuf, gyrB, hup, ftsY, the unc operon, the genes for two M. hominis-specific antigenic membrane proteins, and one gene encoding a protein with some homology to Escherichia coli alanyl-tRNA synthetase. The positions of mapped loci were partially conserved in the five strains except in one strain in which a 300-kb fragment was inverted. The numbers and order of mapped restriction sites were only partly conserved, and this conservation was restricted to certain regions. The gene order was compared with the gene order established for other bacteria and was found to be identical to that of the phylogenetically related Clostridium perfringens. The genome size of the M. hominis strains varied from 704 to 825 kb.
我们展示了5个人型支原体基因组的完整图谱,包括详细的限制性酶切图谱以及多个基因位点的位置。限制性片段通过场反转凝胶电泳或脉冲场凝胶电泳的轮廓夹恒定电场系统进行分离。所有的ApaI、SmaI、BamHI、XhoI和SalI限制性酶切位点(每个菌株共有21至33个位点)都定位在物理图谱上,平均分辨率为26 kb。这些图谱采用三种不同方法构建:(i)用一种或两种限制性酶部分或完全切割后的DNA片段大小测定;(ii)用纯化的限制性片段和特异性探针进行杂交分析;(iii)使用连接克隆。通过与rpoA、rpoC、rrn、tuf、gyrB、hup、ftsY、unc操纵子、两个人型支原体特异性抗原膜蛋白基因以及一个与大肠杆菌丙氨酰 - tRNA合成酶有一定同源性的蛋白质基因的基因特异性探针杂交构建遗传图谱。除了一个菌株中一个300 kb的片段发生倒位外,定位位点在这5个菌株中部分保守。定位的限制性酶切位点的数量和顺序仅部分保守,且这种保守仅限于某些区域。将基因顺序与为其他细菌确定的基因顺序进行比较,发现与人型支原体在系统发育上相关的产气荚膜梭菌的基因顺序相同。人型支原体菌株的基因组大小在704至825 kb之间。