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Excision-reintegration at a pneumococcal phase-variable restriction-modification locus drives within- and between-strain epigenetic differentiation and inhibits gene acquisition.pdf (1.96 MB)

Excision-reintegration at a pneumococcal phase-variable restriction-modification locus drives within- and between-strain epigenetic differentiation and inhibits gene acquisition.

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posted on 2019-06-03, 13:59 authored by MJ Kwun, MR Oggioni, M De Ste Croix, SD Bentley, NJ Croucher
Phase-variation of Type I restriction-modification systems can rapidly alter the sequence motifs they target, diversifying both the epigenetic patterns and endonuclease activity within clonally descended populations. Here, we characterize the Streptococcus pneumoniae SpnIV phase-variable Type I RMS, encoded by the translocating variable restriction (tvr) locus, to identify its target motifs, mechanism and regulation of phase variation, and effects on exchange of sequence through transformation. The specificity-determining hsdS genes were shuffled through a recombinase-mediated excision-reintegration mechanism involving circular intermediate molecules, guided by two types of direct repeat. The rate of rearrangements was limited by an attenuator and toxin-antitoxin system homologs that inhibited recombinase gene transcription. Target motifs for both the SpnIV, and multiple Type II, MTases were identified through methylation-sensitive sequencing of a panel of recombinase-null mutants. This demonstrated the species-wide diversity observed at the tvr locus can likely specify nine different methylation patterns. This will reduce sequence exchange in this diverse species, as the native form of the SpnIV RMS was demonstrated to inhibit the acquisition of genomic islands by transformation. Hence the tvr locus can drive variation in genome methylation both within and between strains, and limits the genomic plasticity of S. pneumoniae.

Funding

BBSRC [BB/N002903/1]; Wellcome [098051]; Sir Henry Dale Fellowship, jointly funded by Wellcome and the Royal Society [104169/Z/14/Z to N.J.C.]. Funding for open access charge: BBSRC [BB/N002903/1].

History

Citation

Nucleic Acids Research, 2018, 46 (21), pp. 11438-11453

Author affiliation

/Organisation/COLLEGE OF LIFE SCIENCES/Biological Sciences/Genetics and Genome Biology

Version

  • VoR (Version of Record)

Published in

Nucleic Acids Research

Publisher

Oxford University Press (OUP)

eissn

1362-4962

Acceptance date

2018-10-08

Copyright date

2018

Available date

2019-06-03

Publisher version

https://academic.oup.com/nar/article/46/21/11438/5128927

Notes

DATA AVAILABILITY Accession codes for the sequence data are listed in Supplementary Table S1. SUPPLEMENTARY DATA Supplementary Data are available at NAR Online. https://academic.oup.com/nar/article-lookup/doi/10.1093/nar/gky906#supplementary-data

Language

en

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