Affiliation:
1. Department of Microbiology, School of Medicine, Case Western Reserve University, Cleveland, Ohio 44106
Abstract
The ability of
Escherichia coli
K to support bacteriophage T4rII replication starts to decline at 3 to 6 min after infection by λ. This inhibition appears to depend on expression of the λ
rex
+
gene, since little inhibition was observed following infection by a λ
rex
mutant or by a hybrid bacteriophage λi
434
which lacks a functional
rex
gene. For promotion of the synthesis of
rex
product, cII
+
and N
+
genes are required and can act
trans
, whereas cY
+
, also required, must be
cis
to a
rex
+
gene. These genes presumably play a role in the transcription of the cI-
rex
operon because they are also known to be required for repressor (cI product) synthesis. Functional cIII, O, P genes are not necessary for ample
rex
product synthesis. We also observed full
rex
expression after infection by λ
sus
cI mutants, suggesting that
rex
and repressor are separate gene products and that repressor is not required for inhibition of T4rII replication. We also report experiments with a
rex
mutant that is not leaky when in a lysogen but is sufficiently leaky shortly after infection to cause inhibition of T4rII replication.
Publisher
American Society for Microbiology
Subject
Virology,Insect Science,Immunology,Microbiology
Cited by
27 articles.
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