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Updated: Aug 17, 2026

Following Cell-fate in E. coli After Infection by Phage Lambda
Published on: October 14, 2011
Mutations reducing the activity of c17, a promoter of phage lambda formed by a tandem duplication
Abstract:
We report the isolation of four independently selected mutations (scs) in the c17 promoter of phage lambda that reduce or eliminate the promoter activity. The c17 promoter is not normally present in lambda, and has been shown to be generated by a tandem duplication which creates a "Pribnow Box," a heptamer sequence implicated in promoter activity. This sequence is located upstream from the site of transcription initiation and is present, with some variation, in all promoters whose sequences have been determined. Analysis of the c17 duplications carrying the scs mutations reveals that three of these mutants carry single base-pair changes in the most highly conserved base pairs of the Pribnow Box and that the other mutation is a reversion to the wild type sequence in this region (i.e., a loss of the duplicated base pairs).
Insights
Researchers identified four mutations in the phage lambda c17 promoter that decrease its activity. These mutations affect the critical "Pribnow Box" sequence, crucial for transcription initiation.
Area of Science:
- Molecular Biology
- Genetics
- Virology
Background:
- The phage lambda c17 promoter is not naturally occurring and arises from a tandem duplication.
- This duplication generates a functional
- Pribnow Box,
- a conserved DNA sequence essential for promoter activity and transcription initiation.
Purpose of the Study:
- To isolate and characterize mutations affecting the activity of the phage lambda c17 promoter.
- To investigate the role of the Pribnow Box sequence in promoter function.
Main Methods:
- Isolation of independently selected mutations (scs) in the c17 promoter region of phage lambda.
- Sequence analysis of the c17 promoter duplications carrying the scs mutations.
Main Results:
- Four scs mutations were identified, all reducing or eliminating c17 promoter activity.
- Three mutations involved single base-pair changes within highly conserved regions of the Pribnow Box.
- One mutation represented a reversion to the wild-type sequence, indicating the loss of duplicated base pairs.
Conclusions:
- The Pribnow Box sequence is critical for phage lambda c17 promoter activity.
- Specific base-pair alterations within the Pribnow Box can significantly impair or abolish promoter function.
- The study provides insights into the structure-function relationship of bacterial promoters.
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