Nölling J, de Vos W M
Department of Microbiology, Wageningen Agricultural University, The Netherlands.
Nucleic Acids Res. 1992 Oct 11;20(19):5047-52. doi: 10.1093/nar/20.19.5047.
Two CTAG-recognizing restriction and modification (R/M) systems, designated MthZI and MthFI, were identified in the thermophilic archaeon Methanobacterium thermoformicicum strains Z-245 and FTF, respectively. Further analysis revealed that the methyltransferase (MTase) genes are plasmid-located in both strains. The plasmid pFZ1-encoded mthZIM gene of strain Z-245 was further characterized by subcloning and expression studies in Escherichia coli followed by nucleotide sequence analysis. The mthZIM gene is 1065 bp in size and may code for a protein of 355 amino acids (M(r) 42,476 Da). The deduced amino acid sequence of the M.MthZI enzyme shares substantial similarity with four distinct regions from several m4C- and m6A-MTases, and contains the TSPPY motif that is so far only found in m4C-MTases. Partially overlapping with the mthZIM gene and in reverse orientation, an additional ORF was identified with a size of 606 bp potentially coding for a protein of 202 amino acids (M(r) 23.710 Da). This ORF is suggested to encode the corresponding endonuclease R.MthZI.
在嗜热古菌热甲酸甲烷杆菌菌株Z - 245和FTF中分别鉴定出两种识别CTAG的限制与修饰(R/M)系统,分别命名为MthZI和MthFI。进一步分析表明,这两种菌株中的甲基转移酶(MTase)基因都位于质粒上。通过在大肠杆菌中进行亚克隆和表达研究,随后进行核苷酸序列分析,对菌株Z - 245中质粒pFZ1编码的mthZIM基因进行了进一步表征。mthZIM基因大小为1065 bp,可能编码一个由355个氨基酸组成的蛋白质(分子量42,476 Da)。推导的M.MthZI酶的氨基酸序列与几种m4C和m6A甲基转移酶的四个不同区域具有高度相似性,并且包含迄今为止仅在m4C甲基转移酶中发现的TSPPY基序。与mthZIM基因部分重叠且方向相反,鉴定出一个额外的开放阅读框(ORF),大小为606 bp,可能编码一个由202个氨基酸组成的蛋白质(分子量23,710 Da)。该开放阅读框被认为编码相应的内切酶R.MthZI。