ArticleNucleic acids research2025
Orchestrated long-distance gene activation by a ParB-like BisD-CTP DNA clamp in low-frequency transfer competence development in Pseudomonas putida.
Article in Nucleic acids research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
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Who cites it
5 citing papers in PubMed.
- Horizontal transfer of ICEJournal of bacteriology · 2026Article
- Plasmid-encoded host reprogramming promotes plasmid dissemination.bioRxiv : the preprint server for biology · 2026Article
- Article
- Versatile NTP recognition and domain fusions expand the functional repertoire of the ParB-CTPase fold beyond chromosome segregation.Proceedings of the National Academy of Sciences of the United States of America · 2025Article
- The repressor PrtR1 and the global H-NS-like regulators MvaT and MvaV enable the fine-tuning of R-tailocin expression in Pseudomonas protegens.BMC microbiology · 2025Article
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Authors and funding
5 authors.
Funding
Abstract
Integrative conjugative elements (ICEs) are mobile DNA that remain integrated within the host bacterial genome until they activate their excision and transfer. ICE transfer is initiated in a small subpopulation of cells that leads to transfer competence. Here we study the role of the ParB-like protein BisD for ICEclc transfer competence formation in Pseudomonas putida. Genetic dissection and single cell microscopy showed that mCherry-BisD fusion proteins form fluorescent foci on parS-like DNA sequences on ICEclc. Chromatin immunoprecipitation followed by DNA sequencing showed that BisD accumulates at two bisS sites, and further enriches around 11 ICEclc transfer competence promoters. BisD enrichments suggest its sliding over ca. 50 kb of ICE-DNA in an asymmetric manner, following the direction of inwards ICE gene transcription. BisD has a unique domain absent from ParB, which is essential for ICE promoter activation in conjunction with the ICEclc encoded factor BisC, and for ICE transfer. Similar to ParB, purified BisD preferentially binds and hydrolyses cytidine triphosphate (CTP). Mutation of a conserved Arg- at position 95 to an Ala-residue abolished nucleotide binding by BisD, and also inhibited ICE promoter activation and transfer. BisD action might thus serve two purposes, orchestrating ICE gene activation and ICE-DNA clamping.
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