Raleigh E A, Trimarchi R, Revel H
New England BioLabs, Beverly, Massachusetts 01915-9990.
Genetics. 1989 Jun;122(2):279-96. doi: 10.1093/genetics/122.2.279.
We have genetically analyzed, cloned and physically mapped the modified cytosine-specific restriction determinants mcrA (rglA) and mcrB (rglB) of Escherichia coli K-12. The independently discovered Rgl and Mcr restriction systems are shown to be identical by three criteria: 1) mutants with the RglA- or RglB- phenotypes display the corresponding McrA- or McrB- phenotypes, and vice versa; 2) the gene(s) for RglA and McrA reside together at one locus, while gene(s) for RglB and McrB are coincident at a different locus; and 3) RglA+ and RglB+ recombinant clones complement for the corresponding Mcr-deficient lesions. The mcrA (rglA) gene(s) is on the excisable element e14, just clockwise of purB at 25 min. The mcrB (rglB) gene(s), at 99 min, is in a cluster of restriction functions that includes hsd and mrr, determinants of host-specific restriction (EcoK) and methyladenine-specific restriction respectively. Gene order is mcrB-hsdS-hsdM-hsdR-mrr-serB. Possible models for the acqusition of these restriction determinants by enteric bacteria are discussed.
我们对大肠杆菌K-12的修饰胞嘧啶特异性限制决定簇mcrA(rglA)和mcrB(rglB)进行了基因分析、克隆和物理定位。通过三个标准表明独立发现的Rgl和Mcr限制系统是相同的:1)具有RglA或RglB表型的突变体表现出相应的McrA或McrB表型,反之亦然;2)RglA和McrA的基因位于同一基因座,而RglB和McrB的基因在不同基因座重合;3)RglA+和RglB+重组克隆可互补相应的Mcr缺陷型损伤。mcrA(rglA)基因位于可切除元件e14上,在25分钟处,刚好在purB的顺时针方向。mcrB(rglB)基因在99分钟处,位于一个限制功能簇中,该簇包括hsd和mrr,分别是宿主特异性限制(EcoK)和甲基腺嘌呤特异性限制的决定簇。基因顺序为mcrB-hsdS-hsdM-hsdR-mrr-serB。讨论了肠道细菌获得这些限制决定簇的可能模型。