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Author Notes:

Correspondence and requests for materials should be addressed to F.L. (email: lengf@fiu.edu)

F.L. designed research; G.F., S.D., X.Z., B.C. and D.D. performed research; P.C. and B.G. constructed the molecular model; F.L. analyzed data; F.L. wrote the paper.

We thank Kathleen S. Matthews for providing us with E. coli strains containing plasmids overexpressing E. coli lac repressor and mutants. We also thank Dr. Alberto Martin at the University of Toronto for providing us with E. coli strain MG1655(DE3). We are grateful to Dr. Bo Chen for technical support.

The authors declare no competing financial interests.

Subjects:

Research Funding:

This work was supported by grants from the National Institutes of Health: 1SC1HD063059-04 and 1R15GM109254-01A1 (to F.L.) and RGM084070A (to Laura Finzi at Emory University).

Keywords:

  • Bacterial genetics
  • Transcriptional regulatory elements

DNA supercoiling, a critical signal regulating the basal expression of the lac operon in Escherichia coli

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Journal Title:

Scientific Reports

Volume:

Volume 6

Publisher:

, Pages 19243-19243

Type of Work:

Article | Final Publisher PDF

Abstract:

Escherichia coli lac repressor (LacI) is a paradigmatic transcriptional factor that controls the expression of lacZYA in the lac operon. This tetrameric protein specifically binds to the O1, O2 and O3 operators of the lac operon and forms a DNA loop to repress transcription from the adjacent lac promoter. In this article, we demonstrate that upon binding to the O1 and O2 operators at their native positions LacI constrains three (−) supercoils within the 401-bp DNA loop of the lac promoter and forms a topological barrier. The stability of LacI-mediated DNA topological barriers is directly proportional to its DNA binding affinity. However, we find that DNA supercoiling modulates the basal expression from the lac operon in E. coli. Our results are consistent with the hypothesis that LacI functions as a topological barrier to constrain free, unconstrained (−) supercoils within the 401-bp DNA loop of the lac promoter. These constrained (−) supercoils enhance LacI’s DNA-binding affinity and thereby the repression of the promoter. Thus, LacI binding is superhelically modulated to control the expression of lacZYA in the lac operon under varying growth conditions.

Copyright information:

This is an Open Access work distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/).

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