Characterization of a Novel N4-Methylcytosine Restriction-Modification System in Deinococcus radiodurans

Int J Mol Sci. 2024 Jan 29;25(3):1660. doi: 10.3390/ijms25031660.

Abstract

Deinococcus radiodurans is an extremophilic microorganism that possesses a unique DNA damage repair system, conferring a strong resistance to radiation, desiccation, oxidative stress, and chemical damage. Recently, we discovered that D. radiodurans possesses an N4-methylation (m4C) methyltransferase called M.DraR1, which recognizes the 5'-CCGCGG-3' sequence and methylates the second cytosine. Here, we revealed its cognate restriction endonuclease R.DraR1 and recognized that it is the only endonuclease specially for non-4C-methylated 5'-CCGCGG-3' sequence so far. We designated the particular m4C R.DraR1-M.DraR1 as the DraI R-M system. Bioinformatics searches displayed the rarity of the DraI R-M homologous system. Meanwhile, recombination and transformation efficiency experiments demonstrated the important role of the DraI R-M system in response to oxidative stress. In addition, in vitro activity experiments showed that R.DraR1 could exceptionally cleave DNA substrates with a m5C-methlated 5'-CCGCGG-3' sequence instead of its routine activity, suggesting that this particular R-M component possesses a broader substrate choice. Furthermore, an imbalance of the DraI R-M system led to cell death through regulating genes involved in the maintenance of cell survival such as genome stability, transporter, and energy production. Thus, our research revealed a novel m4C R-M system that plays key roles in maintaining cell viability and defending foreign DNA in D. radiodurans.

Keywords: Deinococcus radiodurans; R-M system; methyltransferase; restriction endonuclease.

MeSH terms

  • Bacterial Proteins / metabolism
  • DNA / metabolism
  • DNA Repair
  • DNA Restriction-Modification Enzymes / genetics
  • DNA Restriction-Modification Enzymes / metabolism
  • Deinococcus* / genetics
  • Deinococcus* / metabolism
  • Oxidative Stress

Substances

  • DNA Restriction-Modification Enzymes
  • DNA
  • Bacterial Proteins