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Stationary Phase Induction of DnaN and RecF, Two Genes of Escherichia Coli Involved in DNA Replication and Repair

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Journal EMBO J
Date 1998 May 2
PMID 9501104
Citations 11
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Abstract

The beta subunit of DNA polymerase III holoenzyme, the Escherichia coli chromosomal replicase, is a sliding DNA clamp responsible for tethering the polymerase to DNA and endowing it with high processivity. The gene encoding beta, dnaN, maps between dnaA and recF, which are involved in initiation of DNA replication at oriC and resumption of DNA replication at disrupted replication forks, respectively. In exponentially growing cells, dnaN and recF are expressed predominantly from the dnaA promoters. However, we have found that stationary phase induction of the dnaN promoters drastically changes the expression pattern of the dnaA operon genes. As a striking consequence, synthesis of the beta subunit and RecF protein increases when cell metabolism is slowing down. Such an induction is dependent on the stationary phase sigma factor, RpoS, although the accumulation of this factor alone is not sufficient to activate the dnaN promoters. These promoters are located in DNA regions without static bending, and the -35 hexamer element is essential for their RpoS-dependent induction. Our results suggest that stationary phase-dependent mechanisms have evolved in order to coordinate expression of dnaN and recF independently of the dnaA regulatory region. These mechanisms might be part of a developmental programme aimed at maintaining DNA integrity under stress conditions.

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References
1.
Ohmori H, Kimura M, Nagata T, Sakakibara Y . Structural analysis of the dnaA and dnaN genes of Escherichia coli. Gene. 1984; 28(2):159-70. DOI: 10.1016/0378-1119(84)90253-1. View

2.
Kusano S, Ishihama A . Stimulatory effect of trehalose on formation and activity of Escherichia coli RNA polymerase E sigma38 holoenzyme. J Bacteriol. 1997; 179(11):3649-54. PMC: 179160. DOI: 10.1128/jb.179.11.3649-3654.1997. View

3.
Armengod M, Lambies E . Transcriptional organization of the dnaN and recF genes of Escherichia coli K-12. J Biol Chem. 1988; 263(24):12109-14. View

4.
Quinones A, Messer W . Discoordinate gene expression in the dnaA-dnaN operon of Escherichia coli. Mol Gen Genet. 1988; 213(1):118-24. DOI: 10.1007/BF00333407. View

5.
Kleiner D, Paul W, Merrick M . Construction of multicopy expression vectors for regulated over-production of proteins in Klebsiella pneumoniae and other enteric bacteria. J Gen Microbiol. 1988; 134(7):1779-84. DOI: 10.1099/00221287-134-7-1779. View