Transposition with Tn<i>3</i>-family elements occurs through interaction with the host β-sliding clamp processivity factor

Tn3 family transposons are a widespread group of replicative transposons, notorious for contributing to the dissemination of antibiotic resistance, particularly the global prevalence of carbapenem resistance. The transposase (TnpA) of these elements catalyzes DNA breakage and rejoining reactions required for transposition. However, the molecular mechanism for target site selection with these elements remains unclear. Here, we identify a QLxxLR motif in N-terminal of Tn3 TnpAs and demonstrate that this motif allows interaction between TnpA of Tn3 family transposon Tn1721 and the host β-sliding clamp (DnaN), the major processivity factor of the DNA replication machinery. The TnpA-DnaN interaction is essential for Tn1721 transposition. Our work unveils a mechanism whereby Tn3 family transposons can bias transposition into certain replisomes through an interaction with the host replication machinery. This study further expands the diversity of mobile elements that use interaction with the host replication machinery to bias integration.

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Publication Details

Journal
Nucleic Acids Research
Published
2024-08-09
DOI
https://doi.org/10.1093/nar/gkae674
Citations
8
Primary Topic
Advanced biosensing and bioanalysis techniques
Type
article
Field-Weighted Citation Impact
1.87

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article

Transposition with Tn3-family elements occurs through interaction with the host β-sliding clamp processivity factor

Michael T. Petassi, Minggui Wang, Hong‐Yu Ou, Xiaofei Jiang et al.
8 citations
Nucleic Acids Research
Advanced biosensing and bioanalysis techniques
1.87
article

Transposition with Tn3-family elements occurs through interaction with the host β-sliding clamp processivity factor

Michael T. Petassi, Minggui Wang, Hong‐Yu Ou, Xiaofei Jiang, Yumeng Zhang, Yu Tang, Jiahao Guan, Joseph E. Peters, Wenjuan Wu, Jianfeng Zhang, Wei Liang
article en
8 citations

Abstract

Tn3 family transposons are a widespread group of replicative transposons, notorious for contributing to the dissemination of antibiotic resistance, particularly the global prevalence of carbapenem resistance. The transposase (TnpA) of these elements catalyzes DNA breakage and rejoining reactions required for transposition. However, the molecular mechanism for target site selection with these elements remains unclear. Here, we identify a QLxxLR motif in N-terminal of Tn3 TnpAs and demonstrate that this motif allows interaction between TnpA of Tn3 family transposon Tn1721 and the host β-sliding clamp (DnaN), the major processivity factor of the DNA replication machinery. The TnpA-DnaN interaction is essential for Tn1721 transposition. Our work unveils a mechanism whereby Tn3 family transposons can bias transposition into certain replisomes through an interaction with the host replication machinery. This study further expands the diversity of mobile elements that use interaction with the host replication machinery to bias integration.

Nucleic Acids ResearchVol. 52(17)
Ningbo University (CN), Shanghai Jiao Tong University (CN), Cornell University (US), Fudan University (CN), Shanghai East Hospital (CN), Huashan Hospital (CN)
National Natural Science Foundation of China, National Institutes of Health
Openalex Percentile: Top 14%
Advanced biosensing and bioanalysis techniques
1.87
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