
doi: 10.1101/755397 , 10.1038/s41467-020-17606-6 , 10.17863/cam.54828 , 10.17863/cam.73708 , 10.17863/cam.55769
pmid: 32732900
pmc: PMC7394560
doi: 10.1101/755397 , 10.1038/s41467-020-17606-6 , 10.17863/cam.54828 , 10.17863/cam.73708 , 10.17863/cam.55769
pmid: 32732900
pmc: PMC7394560
Abstract The ter region of the bacterial chromosome, where replication terminates, is the last to be segregated before cell division in Escherichia coli . Delayed segregation is controlled by the MatP protein, which binds to specific sites ( matS ) within ter, and interacts with other proteins such as ZapB. Here, we investigate the role of MatP by combining short-time mobility analyses of the ter locus with biochemical approaches. We find that ter mobility is similar to that of a non- ter locus, except when sister ter loci are paired after replication. This effect depends on MatP, the persistence of catenanes, and ZapB. We characterise MatP/DNA complexes and conclude that MatP binds DNA as a tetramer, but bridging matS sites in a DNA-rich environment remains infrequent. We propose that tetramerisation of MatP links matS sites with ZapB and/or with non-specific DNA to promote optimal pairing of sister ter regions until cell division.
/631/337/641/2002, DNA Replication, /631/326/41, Chromosomal Proteins, Non-Histone, Science, Escherichia coli Proteins, Q, article, Cell Cycle Proteins, /631/326/88, Chromosomes, Bacterial, /631/337/641/2358, /14, Article, [SDV] Life Sciences [q-bio], DNA-Binding Proteins, /14/63, /9, Escherichia coli, /14/35, Cell Division
/631/337/641/2002, DNA Replication, /631/326/41, Chromosomal Proteins, Non-Histone, Science, Escherichia coli Proteins, Q, article, Cell Cycle Proteins, /631/326/88, Chromosomes, Bacterial, /631/337/641/2358, /14, Article, [SDV] Life Sciences [q-bio], DNA-Binding Proteins, /14/63, /9, Escherichia coli, /14/35, Cell Division
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