Chromosome organization by a conserved condensin-ParB system in the actinobacterium Corynebacterium glutamicum.
Kati BöhmGiacomo GiacomelliAndreas SchmidtAxel ImhofRomain KoszulMartial MarboutyMarc BramkampPublished in: Nature communications (2020)
Higher-order chromosome folding and segregation are tightly regulated in all domains of life. In bacteria, details on nucleoid organization regulatory mechanisms and function remain poorly characterized, especially in non-model species. Here, we investigate the role of DNA-partitioning protein ParB and SMC condensin complexes in the actinobacterium Corynebacterium glutamicum. Chromosome conformation capture reveals SMC-mediated long-range interactions around ten centromere-like parS sites clustered at the replication origin (oriC). At least one oriC-proximal parS site is necessary for reliable chromosome segregation. We use chromatin immunoprecipitation and photoactivated single-molecule localization microscopy to show the formation of distinct, parS-dependent ParB-nucleoprotein subclusters. We further show that SMC/ScpAB complexes, loaded via ParB at parS sites, mediate chromosomal inter-arm contacts (as previously shown in Bacillus subtilis). However, the MukBEF-like SMC complex MksBEFG does not contribute to chromosomal DNA-folding; instead, this complex is involved in plasmid maintenance and interacts with the polar oriC-tethering factor DivIVA. Our results complement current models of ParB-SMC/ScpAB crosstalk and show that some condensin complexes evolved functions that are apparently uncoupled from chromosome folding.
Keyphrases
- single molecule
- copy number
- transcription factor
- living cells
- atomic force microscopy
- bacillus subtilis
- genome wide
- gene expression
- escherichia coli
- drug delivery
- dna damage
- binding protein
- crispr cas
- molecular dynamics simulations
- oxidative stress
- cancer therapy
- small molecule
- wound healing
- high throughput
- circulating tumor cells
- genetic diversity