期刊
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
卷 105, 期 15, 页码 5827-5832出版社
NATL ACAD SCIENCES
DOI: 10.1073/pnas.0705570105
关键词
bacteriophage lambda; gene regulation; flow cytometry
The lysogenic state of bacteriophage lambda is maintained by CI repressor, which negatively regulates two promoters to block lytic gene expression. Expression of CI is itself controlled by positive and negative feedback as CI binds to OR to regulate the P-RM promoter. In addition to direct interactions with operator DNA, CI tetramers bound at O-L and O-R can come together to form an octamer, looping the DNA that lies between them and allowing O-L to assist with negative regulation of P-RM. We used a fluorescent reporter protein to measure the CI concentration for a set of constructs that differ in their ability to assume various forms of the looped structure. Based on the observed steady-state fluorescence for these constructs, the presence of O-L increases P-RM activation unless both operators can be fully occupied. By calculating the probabilities for the underlying operator configurations present in each construct, two different models for the mechanism of enhanced activation allow us to predict that when the DNA is looped, P-RM activation can be 2- to 4-fold higher than is possible for unlooped DNA. Based on our results, transcriptional regulation for lambda's lysogenic/lytic switch includes both activation and repression due to DNA looping.
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