DNA methylation activates retron Ec86 filaments for antiphage defense

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<sup>+</sup>). 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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Publication Details

Journal
Cell Reports
Published
2024-10-01
DOI
https://doi.org/10.1016/j.celrep.2024.114857
Citations
26
Primary Topic
Autophagy in Disease and Therapy
Type
article
Field-Weighted Citation Impact
10.05
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article

DNA methylation activates retron Ec86 filaments for antiphage defense

Yongqing Cui, Zeyuan Guan, Yibei Chen, Tingting Zou et al.
26 citations
Cell Reports
Autophagy in Disease and Therapy
10.05
article

DNA methylation activates retron Ec86 filaments for antiphage defense

Yongqing Cui, Zeyuan Guan, Yibei Chen, Tingting Zou, Tao Pan, Ming Sun, Shuangshuang Wang, Shuangxia Jin, Hongbo Liu, Chen Wang, Jie Cao, Yanjing Wang, Delin Zhang, Qiang Wang, Yongqi Yin, Jia Xu
article en
26 citations

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<sup>+</sup>). These findings provide insights into the retron Ec86 defense mechanism and underscore an emerging theme of antiphage defense through supramolecular complex assemblies.

Cell ReportsVol. 43(10)
Huazhong Agricultural University (CN)
Openalex Percentile: Top 1%
Autophagy in Disease and Therapy
10.05
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DNA methylation activates retron Ec86 filaments for antiphage defense — Yongqing Cui, Zeyuan Guan, et al. · Cell Reports (2024) | TGRS Research Map | TGRS