Ouellette Matthew, Jackson Laura, Chimileski Scott, Papke R Thane
Department of Molecular and Cell Biology, University of Connecticut Storrs, CT, USA.
Front Microbiol. 2015 Apr 8;6:251. doi: 10.3389/fmicb.2015.00251. eCollection 2015.
Restriction-modification (RM) systems have evolved to protect the cell from invading DNAs and are composed of two enzymes: a DNA methyltransferase and a restriction endonuclease. Although RM systems are present in both archaeal and bacterial genomes, DNA methylation in archaea has not been well defined. In order to characterize the function of RM systems in archaeal species, we have made use of the model haloarchaeon Haloferax volcanii. A genomic DNA methylation analysis of H. volcanii strain H26 was performed using PacBio single molecule real-time (SMRT) sequencing. This analysis was also performed on a strain of H. volcanii in which an annotated DNA methyltransferase gene HVO_A0006 was deleted from the genome. Sequence analysis of H26 revealed two motifs which are modified in the genome: C(m4)TAG and GCA(m6)BN6VTGC. Analysis of the ΔHVO_A0006 strain indicated that it exhibited reduced adenine methylation compared to the parental strain and altered the detected adenine motif. However, protein domain architecture analysis and amino acid alignments revealed that HVO_A0006 is homologous only to the N-terminal endonuclease region of Type IIG RM proteins and contains a PD-(D/E)XK nuclease motif, suggesting that HVO_A0006 is a PD-(D/E)XK nuclease family protein. Further bioinformatic analysis of the HVO_A0006 gene demonstrated that the gene is rare among the Halobacteria. It is surrounded by two transposition genes suggesting that HVO_A0006 is a fragment of a Type IIG RM gene, which has likely been acquired through gene transfer, and affects restriction-modification activity by interacting with another RM system component(s). Here, we present the first genome-wide characterization of DNA methylation in an archaeal species and examine the function of a DNA methyltransferase related gene HVO_A0006.
限制修饰(RM)系统已经进化到可以保护细胞免受入侵DNA的影响,它由两种酶组成:一种DNA甲基转移酶和一种限制内切酶。尽管RM系统存在于古菌和细菌基因组中,但古菌中的DNA甲基化尚未得到很好的定义。为了表征RM系统在古菌物种中的功能,我们利用了嗜盐古菌沃氏嗜盐菌(Haloferax volcanii)作为模型。使用PacBio单分子实时(SMRT)测序对沃氏嗜盐菌H26菌株进行了基因组DNA甲基化分析。对基因组中一个注释的DNA甲基转移酶基因HVO_A0006被删除的沃氏嗜盐菌菌株也进行了此分析。H26的序列分析揭示了基因组中两个被修饰的基序:C(m4)TAG和GCA(m6)BN6VTGC。对ΔHVO_A0006菌株的分析表明,与亲本菌株相比,它的腺嘌呤甲基化减少,并且改变了检测到的腺嘌呤基序。然而,蛋白质结构域分析和氨基酸比对表明,HVO_A0006仅与IIG型RM蛋白的N端内切酶区域同源,并且包含一个PD-(D/E)XK核酸酶基序,这表明HVO_A0006是一种PD-(D/E)XK核酸酶家族蛋白。对HVO_A0006基因的进一步生物信息学分析表明,该基因在嗜盐菌中很少见。它被两个转座基因包围,这表明HVO_A0006是IIG型RM基因的一个片段,可能是通过基因转移获得的,并通过与另一个RM系统组件相互作用来影响限制修饰活性。在这里,我们展示了古菌物种中DNA甲基化的首次全基因组表征,并研究了与DNA甲基转移酶相关的基因HVO_A0006的功能。