Defining the prototypical DNA replication fork trap in bacteria
Casey J. ToftiD, Morgane J. J. Moreau, Jiřı́ PerůtkaiD, Savitri Mandapati, Peter J. EnyeartiD, Alanna E. SorensoniD, Andrew D. EllingtoniD, Patrick M. SchaefferiD
Abstract
In Escherichia coli, DNA replication termination is orchestrated by two clusters of Ter sites forming a DNA replication fork trap when bound by Tus proteins. The formation of a locked Tus-Ter complex is essential for halting incoming DNA replication forks. However, the absence of replication fork arrest at some Ter sites raised questions about their significance. In this study, we examined the genome-wide distribution of Tus and found that only the six innermost Ter sites (TerA-E and G) were significantly bound by Tus. We also found that a single ectopic insertion of TerB in its non-permissive orientation could not be achieved, advocating against a need for back-up Ter sites. Finally, examination of the genomes of a variety of Enterobacterales revealed a new replication fork trap architecture exclusively found outside the Enterobacteriaceae family. Taken together, our data enabled the delineation of a narrow prototypical Tus-dependent DNA replication fork trap consisting of only two Ter sites. Graphical Abstract O_FIG O_LINKSMALLFIG WIDTH=198 HEIGHT=200 SRC="FIGDIR/small/453168v2_ufig1.gif" ALT="Figure 1"> View larger version (56K): org.highwire.dtl.DTLVardef@feb685org.highwire.dtl.DTLVardef@810368org.highwire.dtl.DTLVardef@6bed9org.highwire.dtl.DTLVardef@dbcff7_HPS_FORMAT_FIGEXP M_FIG C_FIG
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