AI Article Synopsis

  • Retrons are multigene defense systems that protect organisms from phage invasions, involving a reverse transcriptase, non-coding RNA, and effector protein.
  • The study focuses on the retron Ec86 system, discovering that it is triggered by a phage-encoded DNA methyltransferase (Dcm) and activated by methylation of single-stranded DNA.
  • Researchers revealed a specific structure of the Ec86-effector complex that can break down NAD, highlighting how complex assemblies contribute to effective antiphage defenses.

Article Abstract

Retrons are a class of multigene antiphage defense systems typically consisting of a retron reverse transcriptase, a non-coding RNA, and a cognate effector. Although triggers for several retron systems have been discovered recently, the complete mechanism by which these systems detect invading phages and mediate defense remains unclear. Here, we focus on the retron Ec86 defense system, elucidating its modes of activation and mechanisms of action. We identified a phage-encoded DNA cytosine methyltransferase (Dcm) as a trigger of the Ec86 system and demonstrated that Ec86 is activated upon multicopy single-stranded DNA (msDNA) methylation. We further elucidated the structure of a tripartite retron Ec86-effector filament assembly that is primed for activation by Dcm and capable of hydrolyzing nicotinamide adenine dinucleotide (NAD). These findings provide insights into the retron Ec86 defense mechanism and underscore an emerging theme of antiphage defense through supramolecular complex assemblies.

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Source
http://dx.doi.org/10.1016/j.celrep.2024.114857DOI Listing

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