Furuta Yoshikazu
Postdoctoral Fellowship for Research Abroad, JSPS.
Nihon Saikingaku Zasshi. 2015;70(4):383-9. doi: 10.3412/jsb.70.383.
Helicobacter pylori infects human stomach and cause various gastric diseases including gastric cancer. The species is also known for rapid evolution and wide geographical diversity of genome sequence. Our team sequenced whole genome sequences of H. pylori strains isolated from Japanese patients and compared with whole genome sequences of H. pylori strains with other geographic origin and found that not only the gene repertoire but also genome structures and epigenetic modifications such as DNA methylations had large diversity with various mechanisms. Genome inversion events were geography specific and some of them were found to occur with gene duplication at their termini. DNA methylation states of H. pylori genomes suggested that they are diversified by both existence/absence repertoire of methyltransferase genes and by the movement of target recognition domain in the methyltransferase genes. Omics analysis revealed that methylation target sequence and transcriptome status are actually diversified by the domain sequence movement. We suggested that H. pylori utilizes these genome structure and methylome diversity for its adaptive evolution.
幽门螺杆菌感染人类胃部并引发包括胃癌在内的各种胃部疾病。该物种还以基因组序列的快速进化和广泛的地理多样性而闻名。我们的团队对从日本患者中分离出的幽门螺杆菌菌株进行了全基因组测序,并与其他地理来源的幽门螺杆菌菌株的全基因组序列进行了比较,发现不仅基因库,而且基因组结构和诸如DNA甲基化等表观遗传修饰都具有多种机制的巨大多样性。基因组倒位事件具有地理特异性,其中一些被发现是在其末端发生基因复制时出现的。幽门螺杆菌基因组的DNA甲基化状态表明,它们通过甲基转移酶基因的存在/缺失库以及甲基转移酶基因中靶标识别域的移动而多样化。组学分析表明,甲基化靶序列和转录组状态实际上因域序列移动而多样化。我们认为幽门螺杆菌利用这些基因组结构和甲基化组多样性进行适应性进化。