Highlander S K, Garza O
Department of Microbiology and Immunology, Baylor College of Medicine, Houston, TX 77030, USA.
Gene. 1996 Oct 31;178(1-2):89-96. doi: 10.1016/0378-1119(96)00340-x.
Genes encoding the type I restriction-modification (R-M) system of the bovine pathogen, Pasteurella haemolytica, have been identified immediately downstream of a locus that encodes a transcriptional activator of P. haemolytica leukotoxin expression. Type I enzymes are encoded by three genes called hsdM, hsdS and hsdR, and have fallen into three groups, called Ia, Ib and Ic. HsdS provides a sequence recognition function which in concert with HsdM forms an active methyltransferase (MTase). Inclusion of the HsdR subunit in the complex creates an active restriction endonuclease (ENase) capable of cleaving unmethylated target DNA. The P. haemolytica hsdMSR genes were mapped using transposon Tn10d-Cam insertions, and bacteriophage restriction and modification assays in Escherichia coli. We determined the nucleotide sequences of hsdM, hsdS and hsdR, and observed that the deduced amino acid (aa) sequences were very similar to predicted R-M subunits in the respiratory pathogen, Haemophilus influenzae. Phylogenetic comparisons of all known Hsd aa sequences placed the P. haemolytica and H. influenzae proteins into a new group which we labeled the Type Id R-M family. Expression of the P. haemolytica R-M genes in E. coli was inefficient and is likely to be a consequence of the unusual codon usage in P. haemolytica genes.
编码牛病原体溶血巴斯德氏菌I型限制修饰(R-M)系统的基因已在一个编码溶血巴斯德氏菌白细胞毒素表达转录激活因子的基因座下游被鉴定出来。I型酶由三个名为hsdM、hsdS和hsdR的基因编码,并已分为三组,称为Ia、Ib和Ic。HsdS提供序列识别功能,它与HsdM协同形成活性甲基转移酶(MTase)。复合物中包含HsdR亚基会产生一种能够切割未甲基化靶DNA的活性限制内切酶(ENase)。利用转座子Tn10d-Cam插入以及在大肠杆菌中的噬菌体限制和修饰试验对溶血巴斯德氏菌的hsdMSR基因进行了定位。我们测定了hsdM、hsdS和hsdR的核苷酸序列,并观察到推导的氨基酸(aa)序列与呼吸道病原体流感嗜血杆菌中预测的R-M亚基非常相似。对所有已知Hsd aa序列的系统发育比较将溶血巴斯德氏菌和流感嗜血杆菌的蛋白质归为一个新的组,我们将其标记为Id型R-M家族。溶血巴斯德氏菌R-M基因在大肠杆菌中的表达效率低下,这可能是溶血巴斯德氏菌基因中密码子使用异常的结果。