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Microbiology 152 (2006), 1055-1062; DOI  10.1099/mic.0.28624-0
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Microbiology 152 (2006), 1055-1062; DOI  10.1099/mic.0.28624-0
© 2006 Society for General Microbiology

An orphan DNA (cytosine-5-)-methyltransferase in Vibrio cholerae

Sanjib Banerjee and Rukhsana Chowdhury

Biophysics Division, Indian Institute of Chemical Biology, 4 Raja S. C. Mullick Road, Calcutta 700 032, India

Correspondence
Rukhsana Chowdhury
rukhsana{at}iicb.res.in

5-Methyl cytosine (m5C) was detected in genomic DNA of the enteric pathogen Vibrio cholerae by HPLC analysis and immunoblotting with m5C-specific antibody. Although cleavage with the restriction endonuclease EcoRII revealed the absence of a Dcm homologue in V. cholerae, analysis of the genome sequence indicated the presence of a gene, designated in this study as vchM, which encodes a DNA (cytosine-5-)-methyltransferase (m5C-MTase) designated M.Vch. M.Vch is not associated with a restriction endonuclease or a mismatch very short patch repair (Vsr)-like endonuclease and is hence an ‘orphan’ or solitary MTase, although analysis of a phylogenetic tree indicated that related cytosine MTases are all components of restriction-modification systems. M.Vch recognizes and methylates the first 5' C in the degenerate sequence 5'-RCCGGY-3'. RT-PCR analysis suggested that vchM gene expression is increased during the stationary phase of growth. During stationary phase, the spontaneous mutation frequency in the V. cholerae wild-type strain was significantly higher than in the corresponding vchM mutant strain, suggesting that the presence of M.Vch and the absence of a very short patch (VSP) repair-like system imposes upon V. cholerae a mutator phenotype.

Abbreviations: AdoMet, S-adenosyl methionine; m5C, 5-methyl cytosine; MTase, methyltransferase; R-M, restriction-modification; VSP, very short patch (repair system); Vsr, very short patch repair (endonuclease)






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Copyright © 2006 Society for General Microbiology.