SeqA blocking of DnaA-oriC interactions ensures staged assembly of the E. coli pre-RC.

Abstract:

:DnaA occupies only the three highest-affinity binding sites in E. coli oriC throughout most of the cell cycle. Immediately prior to initiation of chromosome replication, DnaA interacts with additional recognition sites, resulting in localized DNA-strand separation. These two DnaA-oriC complexes formed during the cell cycle are functionally and temporally analogous to yeast ORC and pre-RC. After initiation, SeqA binds to hemimethylated oriC, sequestering oriC while levels of active DnaA are reduced, preventing reinitiation. In this paper, we investigate how resetting of oriC to the ORC-like complex is coordinated with SeqA-mediated sequestration. We report that oriC resets to ORC during sequestration. This was possible because SeqA blocked DnaA binding to hemimethylated oriC only at low-affinity recognition sites associated with GATC but did not interfere with occupation of higher-affinity sites. Thus, during the sequestration period, SeqA repressed pre-RC assembly while ensuring resetting of E. coli ORC.

journal_name

Mol Cell

journal_title

Molecular cell

authors

Nievera C,Torgue JJ,Grimwade JE,Leonard AC

doi

10.1016/j.molcel.2006.09.016

subject

Has Abstract

pub_date

2006-11-17 00:00:00

pages

581-92

issue

4

eissn

1097-2765

issn

1097-4164

pii

S1097-2765(06)00664-2

journal_volume

24

pub_type

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