Sullivan K M, Saunders J R
Department of Genetics and Microbiology, University of Liverpool, UK.
Mol Gen Genet. 1989 Apr;216(2-3):380-7. doi: 10.1007/BF00334379.
The NgoPII restriction endonuclease, which recognizes the sequence 5'-GG decreases CC-3', differs from its isoschizomer HaeIII in being sensitive to methylation at the external cytosine residue. The entire nucleotide sequence of a cloned 3.3 kb segment of Neisseria gonorrhoeae strain P9 chromosomal DNA which harbours the NgoPII restriction-modification system has been determined. This data, coupled with sub-cloning experiments, indicates that the restriction endonuclease (R.NgoII) and modification (M.NgoII) genes are transcribed from separate promoters but are arranged in tandem, with the R.NgoPII gene being located on the 5' side of the M.NgoPII gene. Unlike all previously reported restriction systems the 3' end of the endonuclease open reading frame overlaps the 5' end of the methylase open reading frame by 8 codons. This overlap may have implications for the regulation of the NgoPII restriction-modification system.
NgoPII限制性内切酶识别序列5'-GG↓CC-3',与其同裂酶HaeIII的不同之处在于,它对外侧胞嘧啶残基的甲基化敏感。已确定淋病奈瑟菌P9菌株染色体DNA中一个携带NgoPII限制修饰系统的3.3 kb克隆片段的完整核苷酸序列。这些数据与亚克隆实验表明,限制性内切酶(R.NgoII)基因和甲基化(M.NgoII)基因从不同的启动子转录,但串联排列,R.NgoPII基因位于M.NgoPII基因的5'端。与所有先前报道的限制系统不同,内切酶开放阅读框的3'端与甲基化酶开放阅读框的5'端重叠8个密码子。这种重叠可能对NgoPII限制修饰系统的调控有影响。