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Conjugative transfer of the IncN plasmid pKM101 is mediated by dynamic interactions between the TraK accessory factor and TraI relaxase
Department of Microbiology and Molecular Genetics, McGovern Medical School at UTHealth Houston, TX, United States.
Umeå University, Faculty of Medicine, Department of Medical Biochemistry and Biophysics. Umeå University, Faculty of Medicine, Umeå Centre for Microbial Research (UCMR). Umeå University, Faculty of Medicine, Wallenberg Centre for Molecular Medicine at Umeå University (WCMM).ORCID iD: 0000-0002-6664-5165
Umeå University, Faculty of Medicine, Department of Medical Biochemistry and Biophysics. Umeå University, Faculty of Medicine, Umeå Centre for Microbial Research (UCMR). Umeå University, Faculty of Medicine, Wallenberg Centre for Molecular Medicine at Umeå University (WCMM).ORCID iD: 0000-0001-6848-322x
Department of Microbiology and Molecular Genetics, McGovern Medical School at UTHealth Houston, TX, United States.
2024 (English)In: FEBS Letters, ISSN 0014-5793, E-ISSN 1873-3468, Vol. 598, no 21, p. 2717-2733Article in journal (Refereed) Published
Abstract [en]

Conjugative dissemination of mobile genetic elements (MGEs) among bacteria is initiated by assembly of the relaxosome at the MGE's origin-of-transfer (oriT) sequence. A critical but poorly defined step of relaxosome assembly involves recruitment of the catalytic relaxase to its DNA strand-specific nicking site within oriT. Here, we present evidence by AlphaFold modeling, affinity pulldowns, and in vivo site-directed photocrosslinking that the TraK Ribbon–Helix–Helix DNA-binding protein recruits TraI to oriT through a dynamic interaction in which TraI's C-terminal unstructured domain (TraICTD) wraps around TraK's C-proximal tetramerization domain. Upon relaxosome assembly, conformational changes disrupt this contact, and TraICTD instead self-associates as a prerequisite for relaxase catalytic functions or substrate engagement with the transfer channel. These findings delineate key early-stage processing reactions required for conjugative dissemination of a model MGE.

Place, publisher, year, edition, pages
John Wiley & Sons, 2024. Vol. 598, no 21, p. 2717-2733
Keywords [en]
antibiotic resistance, conjugation, horizontal DNA transfer, mobile genetic elements, relaxase, type IV secretion
National Category
Biochemistry Molecular Biology
Identifiers
URN: urn:nbn:se:umu:diva-229657DOI: 10.1002/1873-3468.15011ISI: 001309880900001PubMedID: 39245885Scopus ID: 2-s2.0-85203370025OAI: oai:DiVA.org:umu-229657DiVA, id: diva2:1897816
Funder
Swedish Research Council, 2016-03599Swedish Research Council, 2023-02423Knut and Alice Wallenberg FoundationThe Kempe Foundations, SMK-1869Available from: 2024-09-16 Created: 2024-09-16 Last updated: 2025-02-20Bibliographically approved
In thesis
1. Exploring the diversity of conjugative type IV secretion systems
Open this publication in new window or tab >>Exploring the diversity of conjugative type IV secretion systems
2024 (English)Doctoral thesis, comprehensive summary (Other academic)
Abstract [en]

The increase of antibiotic resistance is a major threat to human health. The spread of mobile genetic elements (MGEs) via conjugation is a major contributor to this problem, especially in hospital settings. Many MGEs encode Type IV Secretion Systems (T4SSs), which are multiprotein complexes that transfer the MGE from donor to recipient cells. T4SSs are versatile systems that exist in all prokaryotes. While most research has focused on T4SSs from Gram negative (G) bacteria, it is important to understand the similarities and differences with T4SSs from Gram positive (G+) bacteria, given their different cell envelopes. Additionally, there is also variability within G T4SSs, which is not yet fully understood.

The aim of this thesis was to explore the diversity of T4SSs, using pKM101 from E. coli (G) and pCF10 from E. faecalis (G+) as model systems, with a focus on DNA transfer and replication (Dtr) proteins.

We biochemically characterized the relaxase TraI from pKM101, which processes plasmid DNA prior to transfer through the T4SS. We also solved the crystal structure of its transesterase domain with and without its substrate oriT DNA, highlighting its conserved mechanism of action. We further explored the relationship between TraI and the accessory protein TraK, using AlphaFold to predict an interaction involving the TraI CTD. This was confirmed experimentally using in vivo BPA-crosslinking.

Many conjugative plasmids encode single-stranded DNA-binding proteins (SSBs), which are thought to protect DNA during transfer. pCF10 encodes the protein PrgE, which was proposed to be one such SSB. However, our biochemical studies and X-ray crystallography revealed that PrgE is an OB-fold protein with unexpected DNA-binding behavior. While its benefit for the plasmid remains unclear, our functional studies have shown that it does not play a role in conjugation.

Finally, we analyzed the structural diversity of conjugative T4SSs in G and G+ bacteria, using bioinformatics and structural modelling. This revealed unknown commonalities, which indicate that G+ T4SS mating channels are likely more similar in structure to G T4SSs than expected.

In summary, this thesis provides new insights into the Dtr proteins that play an integral role in T4SS mediated conjugation, knowledge that hopefully can be used in the fight against hospital acquired infections in the future.

Place, publisher, year, edition, pages
Umeå: Umeå University, 2024. p. 60
Series
Umeå University medical dissertations, ISSN 0346-6612 ; 2325
Keywords
Antibiotic resistance, Horizontal gene transfer, Conjugation, Type IV Secretion Systems, Relaxases, Single-stranded DNA-binding proteins, Biochemistry, Structural Biology
National Category
Structural Biology Biochemistry Molecular Biology
Research subject
Biochemistry
Identifiers
urn:nbn:se:umu:diva-229972 (URN)978-91-8070-495-3 (ISBN)978-91-8070-496-0 (ISBN)
Public defence
2024-10-24, Carl Kempe salen (KBE303), KBC-huset, Linnaeus väg 6, Umeå, 09:00 (English)
Opponent
Supervisors
Available from: 2024-10-01 Created: 2024-09-24 Last updated: 2025-02-20Bibliographically approved

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Breidenstein, AnnikaBerntsson, Ronnie P.-A.

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FEBS Letters
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