Ying Jianchao, Wang Huifeng, Bao Bokan, Zhang Ying, Zhang Jinfang, Zhang Cheng, Li Aifang, Lu Junwan, Li Peizhen, Ying Jun, Liu Qi, Xu Teng, Yi Huiguang, Li Jinsong, Zhou Li, Zhou Tieli, Xu Zuyuan, Ni Liyan, Bao Qiyu
1. Institute of Biomedical Informatics/Zhejiang Provincial Key Laboratory of Medical Genetics, Wenzhou Medical University, Wenzhou 325035, China.
1. Institute of Biomedical Informatics/Zhejiang Provincial Key Laboratory of Medical Genetics, Wenzhou Medical University, Wenzhou 325035, China ; 2. National Institute of Biological Sciences, Beijing 102206, China.
Int J Biol Sci. 2015 Jan 1;11(1):11-21. doi: 10.7150/ijbs.10320. eCollection 2015.
The homocysteine methyltransferase encoded by mmuM is widely distributed among microbial organisms. It is the key enzyme that catalyzes the last step in methionine biosynthesis and plays an important role in the metabolism process. It also enables the microbial organisms to tolerate high concentrations of selenium in the environment. In this research, 533 mmuM gene sequences covering 70 genera of the bacteria were selected from GenBank database. The distribution frequency of mmuM is different in the investigated genera of bacteria. The mapping results of 160 mmuM reference sequences showed that the mmuM genes were found in 7 species of pathogen genomes sequenced in this work. The polymerase chain reaction products of one mmuM genotype (NC_013951 as the reference) were sequenced and the sequencing results confirmed the mapping results. Furthermore, 144 representative sequences were chosen for phylogenetic analysis and some mmuM genes from totally different genera (such as the genes between Escherichia and Klebsiella and between Enterobacter and Kosakonia) shared closer phylogenetic relationship than those from the same genus. Comparative genomic analysis of the mmuM encoding regions on plasmids and bacterial chromosomes showed that pKF3-140 and pIP1206 plasmids shared a 21 kb homology region and a 4.9 kb fragment in this region was in fact originated from the Escherichia coli chromosome. These results further suggested that mmuM gene did go through the gene horizontal transfer among different species or genera of bacteria. High-throughput sequencing combined with comparative genomics analysis would explore distribution and dissemination of the mmuM gene among bacteria and its evolution at a molecular level.
由mmuM编码的同型半胱氨酸甲基转移酶广泛分布于微生物中。它是催化甲硫氨酸生物合成最后一步的关键酶,在代谢过程中起重要作用。它还使微生物能够耐受环境中的高浓度硒。在本研究中,从GenBank数据库中选择了覆盖70个细菌属的533条mmuM基因序列。mmuM在被研究的细菌属中的分布频率不同。160条mmuM参考序列的定位结果表明,在本研究测序的7种病原体基因组中发现了mmuM基因。对一种mmuM基因型(以NC_013951为参考)的聚合酶链反应产物进行测序,测序结果证实了定位结果。此外,选择144条代表性序列进行系统发育分析,一些来自完全不同属的mmuM基因(如大肠杆菌和克雷伯菌之间以及肠杆菌和科索科尼亚菌之间的基因)的系统发育关系比来自同一属的基因更密切。对质粒和细菌染色体上mmuM编码区的比较基因组分析表明,pKF3 - 140和pIP1206质粒共享一个21 kb的同源区域,该区域中的一个4.9 kb片段实际上起源于大肠杆菌染色体。这些结果进一步表明mmuM基因确实在不同种或属的细菌之间发生了基因水平转移。高通量测序结合比较基因组分析将在分子水平上探索mmuM基因在细菌中的分布、传播及其进化。