Type II restriction modification system in Ureaplasma parvum OMC-P162 strain.
Heng Ning WuYukiko NakuraMichinobu YoshimuraOurlad Alzeus Gaddi TantengcoMakoto NomiyamaToshimitsu TakayanagiTomio FujitaKiyoshi YasukawaItaru YanagiharaPublished in: PloS one (2018)
Ureaplasma parvum serovar 3 strain, OMC-P162, was isolated from the human placenta of a preterm delivery at 26 weeks' gestation. In this study, we sequenced the complete genome of OMC-P162 and compared it with other serovar 3 strains isolated from patients with different clinical conditions. Ten unique genes in OMC-P162, five of which encoded for hypothetical proteins, were identified. Of these, genes UPV_229 and UPV_230 formed an operon whose open reading frames were predicted to code for a DNA methyltransferase and a hypothetical protein, respectively. DNA modification analysis of the OMC-P162 genome identified N4-methylcytosine (m4C) and N6-methyladenine (m6A), but not 5-methylocytosine (m5C). UPV230 recombinant protein displayed endonuclease activity and recognized the CATG sequence, resulting in a blunt cut between A and T. This restriction enzyme activity was identical to that of the cultivated OMC-P162 strain, suggesting that this restriction enzyme was naturally expressed in OMC-P162. We designated this enzyme as UpaP162. Treatment of pT7Blue plasmid with recombinant protein UPV229 completely blocked UpaP162 restriction enzyme activity. These results suggest that the UPV_229 and UPV_230 genes act as a type II restriction-modification system in Ureaplasma OMC-P162.
Keyphrases
- genome wide
- escherichia coli
- amino acid
- protein protein
- cell free
- gestational age
- endothelial cells
- bioinformatics analysis
- genome wide identification
- preterm infants
- minimally invasive
- dna methylation
- binding protein
- working memory
- single molecule
- crispr cas
- gene expression
- oxidative stress
- circulating tumor
- pluripotent stem cells
- smoking cessation