Modified DNA substrate selectivity by GmrSD-family Type IV restriction enzyme BrxU

Bacteriophages (phages), viral predators of bacteria, generate selection pressure that causes bacteria to evolve defence systems. Type I, II and III restriction enzymes cleave incoming non-modified phage DNAs. Phages have evolved to defend against these restriction systems by modifying their DNA so that they are no longer suitable substrates. Type IV restriction enzymes have evolved to recognize and cleave modified DNA. We have recently characterized and solved the first structure for the Type IV GmrSD-family enzymes, using the BrxU homologue from <i>Escherichia fergusonii</i>. Though promiscuous in target modifications, little is known about BrxU substrate preference. We used modified DNAs in <i>in vitro</i> assays to characterize the substrate preferences of BrxU and investigate the impact of the GmrSD-inhibitor IPI* on BrxU activity. These data extend our knowledge of phage-host interactions and inform mechanistic studies on the reaction cycle of BrxU and GmrSD homologues.This article is part of the discussion meeting issue 'The ecology and evolution of bacterial immune systems'.

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Publication Details

Journal
Philosophical Transactions of the Royal Society B Biological Sciences
Published
2025-09-04
DOI
https://doi.org/10.1098/rstb.2024.0072
Citations
2
Primary Topic
Bacteriophages and microbial interactions
Type
article
Field-Weighted Citation Impact
3.43

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article

Modified DNA substrate selectivity by GmrSD-family Type IV restriction enzyme BrxU

Tim R. Blower, Jennifer J. Readshaw, Peter Weigele, Yan‐Jiun Lee
2 citations
Philosophical Transactions of the Royal Society B Biological Sciences
Bacteriophages and microbial interactions
3.43
article

Modified DNA substrate selectivity by GmrSD-family Type IV restriction enzyme BrxU

Tim R. Blower, Jennifer J. Readshaw, Peter Weigele, Yan‐Jiun Lee
article en
2 citations

Abstract

Bacteriophages (phages), viral predators of bacteria, generate selection pressure that causes bacteria to evolve defence systems. Type I, II and III restriction enzymes cleave incoming non-modified phage DNAs. Phages have evolved to defend against these restriction systems by modifying their DNA so that they are no longer suitable substrates. Type IV restriction enzymes have evolved to recognize and cleave modified DNA. We have recently characterized and solved the first structure for the Type IV GmrSD-family enzymes, using the BrxU homologue from <i>Escherichia fergusonii</i>. Though promiscuous in target modifications, little is known about BrxU substrate preference. We used modified DNAs in <i>in vitro</i> assays to characterize the substrate preferences of BrxU and investigate the impact of the GmrSD-inhibitor IPI* on BrxU activity. These data extend our knowledge of phage-host interactions and inform mechanistic studies on the reaction cycle of BrxU and GmrSD homologues.This article is part of the discussion meeting issue 'The ecology and evolution of bacterial immune systems'.

Philosophical Transactions of the Royal Society B Biological SciencesVol. 380(1934)
New England Biolabs (United States) (US), Durham University (GB), New England Biolabs (China) (CN)
Lister Institute of Preventive Medicine, Biotechnology and Biological Sciences Research Council
Openalex Percentile: Top 8%
Bacteriophages and microbial interactions
3.43
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Modified DNA substrate selectivity by GmrSD-family Type IV restriction enzyme BrxU — Tim R. Blower, Jennifer J. Readshaw, et al. · Philosophical Transactions of the Royal Society B Biological Sciences (2025) | TGRS Research Map | TGRS