Seba Mohammed, Boccard Frederic, Duigou Stéphane
Université Paris-Saclay, CEA, CNRS, Institute for Integrative Biology of the Cell, Gif-sur-Yvette, France.
Elife. 2024 Feb 5;12:RP91185. doi: 10.7554/eLife.91185.
Structural maintenance of chromosomes (SMC) complexes share conserved structures and serve a common role in maintaining chromosome architecture. In the bacterium , the SMC complex MukBEF is necessary for rapid growth and the accurate segregation and positioning of the chromosome, although the specific molecular mechanisms involved are still unknown. Here, we used a number of in vivo assays to reveal how MukBEF controls chromosome conformation and how the MatP/ system prevents MukBEF activity. Our results indicate that the loading of MukBEF occurs preferentially on newly replicated DNA, at multiple loci on the chromosome where it can promote long-range contacts in cis even though MukBEF can promote long-range contacts in the absence of replication. Using Hi-C and ChIP-seq analyses in strains with rearranged chromosomes, the prevention of MukBEF activity increases with the number of sites and this effect likely results from the unloading of MukBEF by MatP. Altogether, our results reveal how MukBEF operates to control chromosome folding and segregation in .
染色体结构维持(SMC)复合物具有保守结构,并在维持染色体结构方面发挥共同作用。在细菌中,SMC复合物MukBEF对于快速生长以及染色体的精确分离和定位是必需的,尽管其中涉及的具体分子机制仍不清楚。在这里,我们使用了多种体内试验来揭示MukBEF如何控制染色体构象以及MatP/系统如何阻止MukBEF的活性。我们的结果表明,MukBEF的加载优先发生在新复制的DNA上,在染色体上的多个位点,即使在没有复制的情况下MukBEF也能促进顺式远距离接触,它在这些位点可以促进远距离接触。在染色体重排的菌株中使用Hi-C和ChIP-seq分析,对MukBEF活性的阻止随着位点数量的增加而增强,这种效应可能是由MatP使MukBEF卸载导致的。总之,我们的结果揭示了MukBEF在细菌中如何控制染色体折叠和分离。