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Multiscale Structuring of the E. coli Chromosome by Nucleoid-Associated and Condensin Proteins
Author(s) -
Virginia S. Lioy,
Axel Cournac,
Martial Marbouty,
Stéphane Duigou,
Julien Mozziconacci,
Olivier Espéli,
Frédéric Boccard,
Romain Koszul
Publication year - 2018
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2017.12.027
Subject(s) - biology , nucleoid , condensin , genetics , chromosome , replication timing , chromosome segregation , origin of replication , circular bacterial chromosome , genome , seqa protein domain , bacterial genome size , dna replication , dna , microbiology and biotechnology , escherichia coli , gene
As in eukaryotes, bacterial genomes are not randomly folded. Bacterial genetic information is generally carried on a circular chromosome with a single origin of replication from which two replication forks proceed bidirectionally toward the opposite terminus region. Here, we investigate the higher-order architecture of the Escherichia coli genome, showing its partition into two structurally distinct entities by a complex and intertwined network of contacts: the replication terminus (ter) region and the rest of the chromosome. Outside of ter, the condensin MukBEF and the ubiquitous nucleoid-associated protein (NAP) HU promote DNA contacts in the megabase range. Within ter, the MatP protein prevents MukBEF activity, and contacts are restricted to ∼280 kb, creating a domain with distinct structural properties. We also show how other NAPs contribute to nucleoid organization, such as H-NS, which restricts short-range interactions. Combined, these results reveal the contributions of major evolutionarily conserved proteins in a bacterial chromosome organization.

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