Cooperative DNA binding by CI repressor is dispensable in a phage λ variant

  1. Andrea C. Babić and
  2. John W. Little*
  1. Department of Biochemistry and Molecular Biophysics and Department of Molecular and Cellular Biology, University of Arizona, Tucson, AZ 85721
  1. Edited by Barbara J. Meyer, University of California, Berkeley, CA, and approved September 21, 2007 (received for review March 17, 2006)

Abstract

Complex gene regulatory circuits contain many interacting components. In principle, all of these components and interactions may be essential to the function of the circuit. Alternatively, some of them may be refinements to a simpler version of the circuit that improve its fitness. In this work, we have tested whether a particular property of a critical regulatory protein, CI, is essential to the behavior of the phage λ regulatory circuit. In the lysogenic state, CI represses the expression of the lytic genes, allowing a stable lysogenic state, by binding cooperatively to six operators. A mutant phage lacking cooperativity because of a change in cI could not form stable lysogens; however, this defect could be suppressed by the addition of mutations that altered two cis-acting sites but did not restore cooperativity. The resulting triple mutant was able to grow lytically, form stable single lysogens, and switch to lytic growth upon prophage induction, showing a threshold response in switching similar to that of wild-type λ. We conclude that cooperative DNA binding by CI is not essential for these properties of the λ circuitry, provided that suppressors increase the level of CI. Unlike wild-type lysogens, mutant lysogens were somewhat unstable under certain growth conditions. We surmise that cooperativity is a refinement to a more basic circuit, and that it affords increased stability to the lysogenic state in response to environmental variations.

Footnotes

  • *To whom correspondence should be addressed at:
    1007 East Lowell Street, Life Sciences South Building, Tucson, AZ 85721.
    E-mail: jlittle{at}u.arizona.edu
  • Author contributions: A.C.B. and J.W.L. designed research, performed research, contributed new reagents/analytic tools, analyzed data, and wrote the paper.

  • The authors declare no conflict of interest.

  • This article is a PNAS Direct Submission.

  • This article contains supporting information online at www.pnas.org/cgi/content/full/0602223104/DC1.

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