Jeon Taeck J
Department of Biology, College of Natural Sciences, Chosun University, Gwangju 501-759, Republic of Korea.
J Microbiol. 2008 Oct;46(5):564-70. doi: 10.1007/s12275-008-0129-8. Epub 2008 Oct 31.
The expression of amoeba sams genes is switched from sams1 to sams2 when amoebae are infected with Legionella jeonii. To elucidate the mechanism for the inactivation of host sams1 gene by endosymbiotic bacteria, methylation states of the sams1 gene of D and xD amoebae was compared in this study. The sams1 gene of amoebae was methylated at an internal adenine residue of GATC site in symbiont-bearing xD amoebae but not in symbiont-free D amoebae, suggesting that the modification might have caused the inactivation of sams1 in xD amoebae. The sams1 gene of xD amoebae was inactivated at the transcriptional level. Analysis of DNA showed that adenine residues in L. jeonii sams were also methylated, implying that L. jeonii bacteria belong to a Dam methylase-positive strain. In addition, both SAM and Met appeared to act as negative regulators for the expression of sams1 whereas the expression of sams2 was not affected in amoebae.
当变形虫被嗜肺军团菌感染时,变形虫sams基因的表达会从sams1切换到sams2。为了阐明内共生细菌使宿主sams1基因失活的机制,本研究比较了D和xD变形虫中sams1基因的甲基化状态。变形虫的sams1基因在携带共生体的xD变形虫的GATC位点的内部腺嘌呤残基处发生甲基化,而在无共生体的D变形虫中未发生甲基化,这表明这种修饰可能导致了xD变形虫中sams1的失活。xD变形虫的sams1基因在转录水平上失活。DNA分析表明,嗜肺军团菌sams中的腺嘌呤残基也发生了甲基化,这意味着嗜肺军团菌属于Dam甲基化酶阳性菌株。此外,SAM和Met似乎都作为sams1表达的负调节因子,而sams2的表达在变形虫中不受影响。