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Journal of Bacteriology, February 2001, p. 1085-1089, Vol. 183, No. 3
Biology Department, Massachusetts Institute
of Technology, Cambridge, Massachusetts 02139
Received 15 September 2000/Accepted 20 October 2000
The Escherichia coli SOS-regulated umuDC
gene products participate in a DNA damage checkpoint control and in
translesion DNA synthesis. Specific interactions involving the UmuD and
UmuD' proteins, both encoded by the umuD gene, and
components of the replicative DNA polymerase, Pol III, appear to be
important for regulating these two biological activities of the
umuDC gene products. Here we show that overproduction of
the
0021-9193/01/$04.00+0 DOI: 10.1128/JB.183.3.1085-1089.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
umuDC-dnaQ Interaction and Its
Implications for Cell Cycle Regulation and SOS Mutagenesis in
Escherichia coli


proofreading subunit of Pol III suppresses the cold sensitivity
normally associated with overexpression of the umuDC gene
products. Our results suggest that this suppression is attributable to
specific interactions between UmuD or UmuD' and the C-terminal domain
of
.
*
Corresponding author. Mailing address: Biology
Department, 68-633, Massachusetts Institute of Technology, 77 Massachusetts Ave., Cambridge, MA 02139. Phone: (617) 253-6716. Fax:
(617) 253-2643. E-mail: gwalker{at}MIT.EDU.
Present address: Section of Microbial Pathogenesis, Boyer Center
for Molecular Medicine, Yale University School of Medicine, New Haven,
CT 06536-0812.
Present address: Department of Pathogen Genetics, Genome
Therapeutics Corporation Waltham, MA 02453.
§
Present address: Department of Biochemistry, University of
California, San Francisco, San Francisco, CA 94143-0448.
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