TY - JOUR
T1 - Re-wiring of energy metabolism promotes viability during hyperreplication stress in E. coli
AU - Charbon, Godefroid
AU - Campion, Christopher
AU - Chan, Siu Hung Joshua
AU - Bjørn, Louise
AU - Weimann, Allan
AU - da Silva, Luís Cláudio Nascimento
AU - Jensen, Peter Ruhdal
AU - Løbner-Olesen, Anders
PY - 2017/1/27
Y1 - 2017/1/27
N2 - Chromosome replication in Escherichia coli is initiated by DnaA. DnaA binds ATP which is essential for formation of a DnaA-oriC nucleoprotein complex that promotes strand opening, helicase loading and replisome assembly. Following initiation, DnaAATP is converted to DnaAADP primarily by the Regulatory Inactivation of DnaA process (RIDA). In RIDA deficient cells, DnaAATP accumulates leading to uncontrolled initiation of replication and cell death by accumulation of DNA strand breaks. Mutations that suppress RIDA deficiency either dampen overinitiation or permit growth despite overinitiation. We characterize mutations of the last group that have in common that distinct metabolic routes are rewired resulting in the redirection of electron flow towards the cytochrome bd-1. We propose a model where cytochrome bd-1 lowers the formation of reactive oxygen species and hence oxidative damage to the DNA in general. This increases the processivity of replication forks generated by overinitiation to a level that sustains viability.
AB - Chromosome replication in Escherichia coli is initiated by DnaA. DnaA binds ATP which is essential for formation of a DnaA-oriC nucleoprotein complex that promotes strand opening, helicase loading and replisome assembly. Following initiation, DnaAATP is converted to DnaAADP primarily by the Regulatory Inactivation of DnaA process (RIDA). In RIDA deficient cells, DnaAATP accumulates leading to uncontrolled initiation of replication and cell death by accumulation of DNA strand breaks. Mutations that suppress RIDA deficiency either dampen overinitiation or permit growth despite overinitiation. We characterize mutations of the last group that have in common that distinct metabolic routes are rewired resulting in the redirection of electron flow towards the cytochrome bd-1. We propose a model where cytochrome bd-1 lowers the formation of reactive oxygen species and hence oxidative damage to the DNA in general. This increases the processivity of replication forks generated by overinitiation to a level that sustains viability.
U2 - 10.1371/journal.pgen.1006590
DO - 10.1371/journal.pgen.1006590
M3 - Journal article
C2 - 28129339
SN - 1553-7390
VL - 13
JO - PLoS Genetics
JF - PLoS Genetics
IS - 1
M1 - e1006590
ER -