Affiliation:
1. Department of Biological Sciences, University at Buffalo, Buffalo, New York
Abstract
ABSTRACT
Our data show that unlike bacteriophage λ, repressor bound at O
L
of bacteriophage 933W has no role in regulation of 933W repressor occupancy of 933W O
R
3 or the transcriptional activity of 933W P
RM
. This finding suggests that a cooperative long-range loop between repressor tetramers bound at O
R
and O
L
does not form in bacteriophage 933W. Nonetheless, 933W forms lysogens, and 933W prophage display a threshold response to UV induction similar to related lambdoid phages. Hence, the long-range loop thought to be important for constructing a threshold response in lambdoid bacteriophages is dispensable. The lack of a loop requires bacteriophage 933W to use a novel strategy in regulating its lysis-lysogeny decisions. As part of this strategy, the difference between the repressor concentrations needed to bind O
R
2 and activate 933W P
RM
transcription or bind O
R
3 and repress transcription from P
RM
is <2-fold. Consequently, P
RM
is never fully activated, reaching only ∼25% of the maximum possible level of repressor-dependent activation before repressor-mediated repression occurs. The 933W repressor also apparently does not bind cooperatively to the individual sites in O
R
and O
L
. This scenario explains how, in the absence of DNA looping, bacteriophage 933W displays a threshold effect in response to DNA damage and suggests how 933W lysogens behave as “hair triggers” with spontaneous induction occurring to a greater extent in this phage than in other lambdoid phages.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Cited by
17 articles.
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