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J. Biol. Chem., Vol. 263, Issue 15, 7124-7130, May, 1988
K Sekimizu, D Bramhill and A Kornberg
Complexes previously identified in the reconstitution of stages in the
initiation of replication of plasmids (oriC) bearing the origin of the
Escherichia coli chromosome have been examined further. These are: (i) an
ATP complex of dnaA protein, (ii) an initial complex of ATP.dnaA protein
with oriC DNA, (iii) an open complex in which a portion of the oriC duplex
has been opened by dnaA protein action, (iv) a prepriming complex of the
open complex with dnaB, dnaC, and HU proteins, and (v) a complex with a
small bubble opened at oriC by dnaB helicase action and by coating with
single strand-binding protein (SSB). Helicase and gyrase actions can
enlarge the bubble; coupling to priming and replication propagates
bidirectional fork movement. Formation and stability of these complexes are
profoundly affected by ATP, Mg2+, and temperature, as well as the levels of
the participating proteins, including HU and SSB. As examples, the open
complex is stable to isolation at a temperature near 38 degrees C but not
at 24 degrees C; the prepriming complex requires an elevated temperature
and high ATP levels for its formation, but is maintained at a low
temperature and is destabilized by Mg2+. These successive steps, subject to
a variety of controls, are designed to open the supercoiled duplex for
priming and bidirectional replication.
Sequential early stages in the in vitro initiation of replication at the origin of the Escherichia coli chromosome
Department of Biochemistry, Stanford University School of Medicine, California 94305.
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