Crosstalk between vertical and horizontal gene transfer: plasmid replication control by a conjugative relaxase

Nucleic Acids Res. 2017 Jul 27;45(13):7774-7785. doi: 10.1093/nar/gkx450.

Abstract

Horizontal gene transfer is a key process in the evolution of bacteria and also represents a source of genetic variation in eukaryotes. Among elements participating in gene transfer, thousands of small (<10 kb) mobile bacterial plasmids that replicate by the rolling circle mechanism represent a driving force in the spread of antibiotic resistances. In general, these plasmids are built as genetic modules that encode a replicase, an antibiotic-resistance determinant, and a relaxase that participates in their conjugative mobilization. Further, they control their relatively high copy number (∼30 copies per genome equivalent) by antisense RNAs alone or combined with a repressor protein. We report here that the MobM conjugative relaxase encoded by the promiscuous plasmid pMV158 participates in regulation of the plasmid copy number by transcriptional repression of the antisense RNA, thus increasing the number of plasmid molecules ready to be horizontally transferred (mobilization) and/or vertically inherited (replication). This type of crosstalk between genetic modules involved in vertical and horizontal gene flow has not been reported before.

MeSH terms

  • Bacterial Proteins / genetics
  • Bacterial Proteins / metabolism*
  • Binding Sites
  • Conjugation, Genetic
  • DNA Copy Number Variations
  • DNA Replication
  • DNA, Bacterial / chemistry
  • DNA, Bacterial / genetics
  • DNA, Bacterial / metabolism
  • DNA, Superhelical / chemistry
  • DNA, Superhelical / genetics
  • DNA, Superhelical / metabolism
  • Drug Resistance, Bacterial / genetics
  • Endodeoxyribonucleases / genetics
  • Endodeoxyribonucleases / metabolism*
  • Escherichia coli / genetics
  • Escherichia coli / metabolism
  • Evolution, Molecular
  • Gene Flow
  • Gene Transfer, Horizontal*
  • Microscopy, Electron
  • Models, Biological
  • Plasmids / genetics*
  • Promoter Regions, Genetic
  • Replicon
  • Streptococcus pneumoniae / genetics
  • Streptococcus pneumoniae / metabolism

Substances

  • Bacterial Proteins
  • DNA, Bacterial
  • DNA, Superhelical
  • Endodeoxyribonucleases
  • MobM protein, bacteria