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PMID: 3040665 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Cloning and characterization of dnaA(Cs), a mutation which leads to overinitiation of DNA replication in Escherichia coli K-12.

Journal of bacteriology ·Vol. 169 ·No. 9 ·1987-09-00 ·Pages 3898-903

Braun RE, O'Day K, Wright A

Abstract

The product of the dnaA gene is essential for the initiation of chromosomal DNA replication in Escherichia coli K-12. A cold-sensitive mutation, dnaA(Cs), was originally isolated as a putative intragenic suppressor of the temperature sensitivity of a dnaA46 mutant (G. Kellenberger-Gujer, A. J. Podhajska, and L. Caro, Mol. Gen. Genet. 162:9-16, 1978). The cold sensitivity of the dnaA(Cs) mutant was attributed to a loss of replication control resulting in overinitiation of DNA replication. We cloned and sequenced the dnaA gene from the dnaA(Cs) mutant and showed that it contains three point mutations in addition to the original dnaA46(Ts) mutation. The dnaA(Cs) mutation was dominant to the wild-type allele. Overproduction of the DnaA(Cs) protein blocked cell growth. In contrast, overproduction of wild-type DnaA protein reduced the growth rate of cells but did not stop cell growth. Thus, the effect of elevated levels of the DnaA(Cs) protein was quite different from that of the wild-type protein under the same conditions.

MeSH Terms
Bacterial Proteins/biosynthesis,genetics Base Sequence Cloning, Molecular Cold Temperature DNA Replication DNA Restriction Enzymes DNA, Bacterial/analysis Deoxyribonuclease EcoRI Escherichia coli/genetics,metabolism Genes, Bacterial Mutation Phenotype Plasmids
Chemicals
Bacterial Proteins DNA, Bacterial DNA Restriction Enzymes Deoxyribonuclease EcoRI
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Braun R E
O'Day K
Wright A
References (28)
28 references, click to expand
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Article Info
Journal
Journal of bacteriology
Abbr.
J Bacteriol
ISSN
0021-9193
Published
1987-09-00
Pages
3898-903
Language
English
Region
United States
NLM ID
2985120R
PMCID
PMC213684
Subset
IM
Grants
NIGMS NIH HHS · GM15837 · United States
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