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Host responses influence on the induction of lambda prophage
- Source :
- Molecular Microbiology
- Publication Year :
- 2008
- Publisher :
- Wiley, 2008.
-
Abstract
- Inactivation of bacteriophage lambda CI repressor leads almost exclusively to lytic development. Prophage induction can be initiated either by DNA damage or by heat treatment of a temperature-sensitive repressor. These two treatments also cause a concurrent activation of either the host SOS or heat-shock stress responses respectively. We studied the effects of these two methods of induction on the lytic pathway by monitoring the activation of different lambda promoters, and found that the lambda genetic network co-ordinates information from the host stress response networks. Our results show that the function of the CII transcriptional activator, which facilitates the lysogenic developmental pathway, is not observed following either method of induction. Mutations in the cro gene restore the CII function irrespective of the induction method. Deletion of the heat-shock protease gene ftsH can also restore CII function following heat induction but not following SOS induction. Our findings highlight the importance of the elimination of CII function during induction as a way to ensure an efficient lytic outcome. We also show that, despite the common inhibitory effect on CII function, there are significant differences in the heat- and SOS-induced pathways leading to the lytic cascade.
- Subjects :
- Ultraviolet Rays
Mitomycin
Repressor
Biology
Microbiology
Bacteriophage
Viral Proteins
SOS Response (Genetics)
Lysogenic cycle
Viral Regulatory and Accessory Proteins
SOS response
Promoter Regions, Genetic
SOS Response, Genetics
Lysogeny
Molecular Biology
Research Articles
Prophage
Temperature
Lambda phage
biology.organism_classification
Bacteriophage lambda
Molecular biology
DNA-Binding Proteins
Repressor Proteins
Lytic cycle
Virus Activation
Transcription Factors
Subjects
Details
- ISSN :
- 13652958 and 0950382X
- Volume :
- 68
- Database :
- OpenAIRE
- Journal :
- Molecular Microbiology
- Accession number :
- edsair.doi.dedup.....da1b2233b415ee83ff62c32f10c7edf9