Niault Théophile, Talavera Ariel, Le Cam Eric, Baconnais Sonia, Skovgaard Ole, Fournes Florian, Wagner Léa, Tamman Hedvig, Thompson Andrew, Echemendia-Blanco Dannele, Guzzi Noa, Garcia-Pino Abel, Mazel Didier, Val Marie-Eve
Institut Pasteur, Université Paris Cité, CNRS UMR3525, Unité Plasticité du Génome Bactérien, Département Génomes et Génétique, Paris, France.
Sorbonne Université, Collège Doctoral, Paris, France.
Nat Commun. 2025 Jan 8;16(1):485. doi: 10.1038/s41467-024-55598-9.
The replication of the two chromosomes in the pathogenic bacterium Vibrio cholerae is coordinated by the binding of initiator protein RctB to a checkpoint sequence, crtS. Replication of crtS on the primary chromosome (Chr1) triggers replication of the secondary chromosome (Chr2), but the details are poorly understood. Here, we analyze RctB binding patterns in the V. cholerae genome across various cell cycle stages. We find that RctB primarily binds to sites inhibiting replication initiation at the Chr2 origin (ori2). This inhibitory effect is counteracted when crtS is replicated on Chr1, causing a shift in RctB binding to sites that activate replication at ori2. Structural analyzes indicate the formation of diverse oligomeric states of RctB, coupled to the allosteric effect of DNA, which determine ori2 accessibility. We propose a synchronization model where, upon replication, crtS locally destabilizes the RctB inhibition complex, releasing the Chr2 replication origin.
致病性细菌霍乱弧菌中两条染色体的复制是由起始蛋白RctB与一个检查点序列crtS的结合来协调的。初级染色体(Chr1)上crtS的复制会触发次级染色体(Chr2)的复制,但其细节尚不清楚。在这里,我们分析了霍乱弧菌基因组在不同细胞周期阶段的RctB结合模式。我们发现,RctB主要结合在抑制次级染色体复制起点(ori2)处复制起始的位点上。当crtS在Chr1上复制时,这种抑制作用会被抵消,导致RctB的结合位点转移到激活ori2处复制的位点上。结构分析表明,RctB形成了不同的寡聚状态,并与DNA的变构效应相关联,这决定了ori2的可及性。我们提出了一个同步模型,即在复制时,crtS会使RctB抑制复合物局部不稳定,从而释放Chr2的复制起点。