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Vol. 273, Issue 2, 713-719, January 9, 1998
From the Departments of Biochemistry and Molecular Biology and
Medicine, University of Miami, School of Medicine,
Miami, Florida 33101
Proliferating cell nuclear antigen (PCNA) is
required for processive DNA synthesis catalyzed by DNA polymerase
The Interdomain Connector Loop of Human PCNA Is Involved in a
Direct Interaction with Human Polymerase
(pol
) and polymerase
. We have shown that the epitope of a human
PCNA inhibitory monoclonal antibody (74B1), which inhibits the PCNA
stimulation of DNA synthesis catalyzed by pol
, maps to residues
121-135, which overlap the interdomain connector loop of PCNA
(residues 119-133). We have mutagenized residues 122-133 of human
PCNA. The mutant proteins were expressed in Escherichia
coli and purified to near-homogeneity. The interactions of the
mutants with antibody 74B1 were examined; mutation of Gly-127 abolished
the recognition by antibody 74B1 in a Western blot analysis, confirming
the epitope assignment of 74B1. Mutations of Val-123, Leu-126, Gly-127,
and Ile-128 affected the ability of PCNA to stimulate DNA synthesis by
pol
in several different assays. These mutations affected the
interactions between PCNA and pol
as determined by enzyme-linked immunosorbent assays. These mutants were also affected in their abilities to form a ternary complex with a DNA template-primer, as
determined by electrophoretic mobility gel shift assays. The findings
show that the interdomain connector loop region is involved in binding
of pol
. This same region is involved in the binding of p21, and our
findings support the view that the mechanism of inhibition of DNA
synthesis by p21 is due to a competition for PCNA binding to pol
.
Copyright © 1998 by The American Society for Biochemistry and Molecular Biology, Inc.
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