Abstract
The McrB restriction system in Escherichia coli K12 causes sequence-specific recognition and inactivation of DNA containing 5-methylcytosine residues. We have previously located the mcrB gene near hsdS at 99 min on the E. coli chromosome and demonstrated that it encodes a 51 kDa polypeptide required for restriction of M.AluI methylated (A-G-5mC-T) DNA. We show here, by analysis of maxicell protein synthesis of various cloned fragments from the mcrB region, that a second protein of approximately 39 kDa is also required for McrB-directed restriction. The new gene, designated mcrC, is adjacent to mcrB and located distally to hsdS. The McrB phenotype has been correlated previously with restriction of 5-hydroxy-methyl-cytosine (HMC)-containing T-even phage DNA that lacks the normal glucose modification of HMC, formally designated RglB (for restriction of glucoseless phage). This report reveals a difference between the previously correlated McrB and RglB restriction systems: while both require the mcrB gene product only the McrB system requires the newly identified mcrC-encoded 39-kDa polypeptide.
MeSH Terms
5-Methylcytosine
Cytosine/analogs & derivatives,metabolism
DNA Restriction-Modification Enzymes/genetics,metabolism
DNA, Bacterial/genetics,metabolism
Escherichia coli/genetics,metabolism
Genetic Complementation Test
Phenotype
Plasmids
Chemicals
DNA Restriction-Modification Enzymes
DNA, Bacterial
5-Methylcytosine
Cytosine
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Ross T K
Department of Microbiology, Louisiana State University, Baton Rouge 70803.
Achberger E C
Braymer H D
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