Identification of a second polypeptide required for McrB restriction of 5-methylcytosine-containing DNA in Escherichia coli K12
- PMID: 2664457
- DOI: 10.1007/BF00334382
Identification of a second polypeptide required for McrB restriction of 5-methylcytosine-containing DNA in Escherichia coli K12
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.
Similar articles
-
Genetic and sequence organization of the mcrBC locus of Escherichia coli K-12.J Bacteriol. 1990 Sep;172(9):4888-900. doi: 10.1128/jb.172.9.4888-4900.1990. J Bacteriol. 1990. PMID: 2203735 Free PMC article.
-
Characterization of the Escherichia coli modified cytosine restriction (mcrB) gene.Gene. 1987;61(3):277-89. doi: 10.1016/0378-1119(87)90191-0. Gene. 1987. PMID: 2833428
-
Nucleotide sequence of the McrB region of Escherichia coli K-12 and evidence for two independent translational initiation sites at the mcrB locus.J Bacteriol. 1989 Apr;171(4):1974-81. doi: 10.1128/jb.171.4.1974-1981.1989. J Bacteriol. 1989. PMID: 2649480 Free PMC article.
-
The Pvu II restriction-modification system: cloning, characterization and use in revealing an E. coli barrier to certain methylases or methylated DNAs.Gene Amplif Anal. 1987;5:227-45. Gene Amplif Anal. 1987. PMID: 3333367 Review. No abstract available.
-
Organization and function of the mcrBC genes of Escherichia coli K-12.Mol Microbiol. 1992 May;6(9):1079-86. doi: 10.1111/j.1365-2958.1992.tb01546.x. Mol Microbiol. 1992. PMID: 1316984 Review.
Cited by
-
Hexameric assembly of the AAA+ protein McrB is necessary for GTPase activity.Nucleic Acids Res. 2019 Jan 25;47(2):868-882. doi: 10.1093/nar/gky1170. Nucleic Acids Res. 2019. PMID: 30521042 Free PMC article.
-
Biology of DNA restriction.Microbiol Rev. 1993 Jun;57(2):434-50. doi: 10.1128/mr.57.2.434-450.1993. Microbiol Rev. 1993. PMID: 8336674 Free PMC article. Review.
-
Overproduction and purification of McrC protein from Escherichia coli K-12.J Bacteriol. 1991 Jun;173(12):3918-20. doi: 10.1128/jb.173.12.3918-3920.1991. J Bacteriol. 1991. PMID: 2050643 Free PMC article.
-
Isolation of temperature-sensitive McrA and McrB mutations and complementation analysis of the McrBC region of Escherichia coli K-12.J Bacteriol. 1991 Jan;173(1):150-5. doi: 10.1128/jb.173.1.150-155.1991. J Bacteriol. 1991. PMID: 1987114 Free PMC article.
-
Nomenclature relating to restriction of modified DNA in Escherichia coli.J Bacteriol. 1991 Apr;173(8):2707-9. doi: 10.1128/jb.173.8.2707-2709.1991. J Bacteriol. 1991. PMID: 2013582 Free PMC article.
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Molecular Biology Databases