Affiliation:
1. State Scientific Research Institute of Genetics and Selection of Industrial Microorganisms, Moscow 113545, Russia,1 and
2. Institut Jacques Monod (Centre National de la Recherche Scientifique, UniversitéParis 7), 75251 Paris Cedex 05, France2
Abstract
ABSTRACT
Two
Escherichia coli
genes, expressed from multicopy plasmids, are shown to cause partial induction of prophage λ in
recA
mutant lysogens. One is
rcsA
, which specifies a positive transcriptional regulator of the
cps
genes, which are involved in capsular polysaccharide synthesis. The other is
dsrA
, which specifies an 85-nucleotide RNA that relieves repression of the
rcsA
gene by histone-like protein H-NS. Genetic contexts known to increase Cps expression also cause RecA-independent λ induction: the
rcsC137
mutation, which causes constitutive Cps expression, and the
lon
and
rcsA3
mutations, which stabilize RcsA. Lambdoid phages 21, φ80, and 434 are also induced by RcsA and DsrA overexpression in
recA
lysogens. Excess λ cI repressor specifically blocks λ induction, suggesting that induction involves repressor inactivation rather than repressor bypass. RcsA-mediated induction requires RcsB, the known effector of the
cps
operon, whereas DsrA-mediated induction is RcsB independent in stationary phase, pointing to the existence of yet another RecA-independent pathway of prophage induction.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Cited by
50 articles.
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