| Literature DB >> 26588462 |
Michael C Chao1,2,3, Shijia Zhu4, Satoshi Kimura1,2,3, Brigid M Davis1,2,3, Eric E Schadt2, Gang Fang4, Matthew K Waldor1,2,3.
Abstract
DNA methylation is a key epigenetic regulator in all domains of life, yet the effects of most bacterial DNA methyltransferases on cellular processes are largely undefined. Here, we used diverse techniques, including bisulfite sequencing, transcriptomics, and transposon insertion site sequencing to extensively characterize a 5-methylcytosine (5mC) methyltransferase, VchM, in the cholera pathogen, Vibrio cholerae. We have comprehensively defined VchM's DNA targets, its genetic interactions and the gene networks that it regulates. Although VchM is a relatively new component of the V. cholerae genome, it is required for optimal V. cholerae growth in vitro and during infection. Unexpectedly, the usually essential σE cell envelope stress pathway is dispensable in ∆vchM V. cholerae, likely due to its lower activation in this mutant and the capacity for VchM methylation to limit expression of some cell envelope modifying genes. Our work illuminates how an acquired DNA methyltransferase can become integrated within complex cell circuits to control critical housekeeping processes.Entities:
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Year: 2015 PMID: 26588462 PMCID: PMC4654547 DOI: 10.1371/journal.pgen.1005666
Source DB: PubMed Journal: PLoS Genet ISSN: 1553-7390 Impact factor: 5.917