Multilevel autoregulation of λ repressor protein CI by DNA looping in vitro

The prophage state of bacteriophage λ is extremely stable and is maintained by a highly regulated level of λ repressor protein, CI, which represses lytic functions. CI regulates its own synthesis in a lysogen by activating and repressing its promoter, PRM. CI participates in long-range interactions involving two regions of widely separated operator sites by generating a loop in the intervening DNA. We investigated the roles of each individual site under conditions that permitted DNA loop formation by using in vitro transcription assays for the first time on supercoiled DNA that mimics in vivo situation. We confirmed that DNA loops generated by oligomerization of CI bound to its operators influence the autoactivation and autorepression of PRM regulation. We additionally report that different configurations of DNA loops are central to this regulation—one configuration further enhances autoactivation and another is essential for autorepression of PRM.

[1]  Molecular recognition and information gain. , 1989, Journal of theoretical biology.

[2]  Susan J. Brown,et al.  Characterization of a doubly mutant derivative of the λ PRM promoter: Effects of mutations on activation of PRM☆ , 1988 .

[3]  Mark Ptashne,et al.  λ Repressor and cro—components of an efficient molecular switch , 1981, Nature.

[4]  R. Sauer,et al.  Isolation of lambda repressor mutants with defects in cooperative operator binding. , 1993, Biochemistry.

[5]  D. Jain,et al.  Structure of a ternary transcription activation complex. , 2004, Molecular cell.

[6]  Haw Yang,et al.  DNA looping can enhance lysogenic CI transcription in phage lambda , 2008, Proceedings of the National Academy of Sciences.

[7]  M. Ptashne,et al.  Gene regulation at the right operator (OR) bacteriophage lambda. I. OR3 and autogenous negative control by repressor. , 1980, Journal of molecular biology.

[8]  M. Lewis,et al.  Crystal structure of the λ repressor and a model for pairwise cooperative operator binding , 2008, Nature.

[9]  Benno Müller-Hill,et al.  Four dimers of λ repressor bound to two suitably spaced pairs of λ operators form octamers and DNA loops over large distances , 1999, Current Biology.

[10]  N. Costantino,et al.  On the role of Cro in lambda prophage induction. , 2005, Proceedings of the National Academy of Sciences of the United States of America.

[11]  Mark Ptashne,et al.  Interactions between DNA-bound repressors govern regulation by the λ phage repressor , 1979 .

[12]  Haw Yang,et al.  A simplified model for lysogenic regulation through DNA looping , 2008, 2008 30th Annual International Conference of the IEEE Engineering in Medicine and Biology Society.

[13]  François Jacob,et al.  Regulation of Repressor Expression in λ , 1970 .

[14]  Victor B. Zhurkin,et al.  Gal repressosome contains an antiparallel DNA loop , 2001, Nature Structural Biology.

[15]  N. Costantino,et al.  On the role of Cro in λ prophage induction , 2005 .

[16]  M. Lewis,et al.  Crystal Structure of the λ Repressor C-Terminal Domain Provides a Model for Cooperative Operator Binding , 2000, Cell.

[17]  D. Mount,et al.  The SOS regulatory system of Escherichia coli , 1982, Cell.

[18]  A. D. Kaiser,et al.  Control of λ Repressor Synthesis , 1971 .

[19]  G. K. Ackers,et al.  Site-specific enthalpic regulation of DNA transcription at bacteriophage lambda OR. , 1992, Biochemistry.

[20]  I. Dodd,et al.  Octamerization of lambda CI repressor is needed for effective repression of P(RM) and efficient switching from lysogeny. , 2001, Genes & development.

[21]  I. Dodd,et al.  Cooperativity in long-range gene regulation by the lambda CI repressor. , 2004, Genes & development.

[22]  C. Zurla,et al.  Novel tethered particle motion analysis of CI protein-mediated DNA looping in the regulation of bacteriophage lambda , 2006 .

[23]  M. Ptashne,et al.  Gene regulation at the right operator (OR) of bacteriophage lambda. III. lambda repressor directly activates gene transcription. , 1980, Journal of molecular biology.

[24]  G. Gussin,et al.  Genetic characterization of a prm- mutant of bacteriophage lambda. , 1973, Virology.

[25]  David Dunlap,et al.  Direct demonstration and quantification of long-range DNA looping by the λ bacteriophage repressor , 2009, Nucleic acids research.

[26]  A. Jeffrey,et al.  How the λ repressor and cro work , 1980, Cell.

[27]  Mark Ptashne,et al.  DNA loops induced by cooperative binding of λ repressor , 1986, Nature.

[28]  M. Kashlev,et al.  DNA sequences in gal operon override transcription elongation blocks. , 2008, Journal of molecular biology.

[29]  G. K. Ackers,et al.  Quantitative model for gene regulation by lambda phage repressor. , 1982, Proceedings of the National Academy of Sciences of the United States of America.

[30]  B. Müller-Hill,et al.  Four dimers of lambda repressor bound to two suitably spaced pairs of lambda operators form octamers and DNA loops over large distances. , 1999, Current biology : CB.

[31]  Ian B. Dodd,et al.  Cooperativity in long-range gene regulation by the λ CI repressor , 2004 .

[32]  M Ptashne,et al.  How the lambda repressor and cro work. , 1980, Cell.

[33]  A. Oppenheim,et al.  Supercoiling, integration host factor, and a dual promoter system, participate in the control of the bacteriophage λ pL promoter☆ , 1992 .

[34]  A. Hochschild,et al.  Specificity determinants for the interaction of lambda repressor and P22 repressor dimers. , 1994, Genes & development.

[35]  M Ptashne,et al.  Autoregulation and function of a repressor in bacteriophage lambda. , 1976, Science.

[36]  M. Ptashne,et al.  Cooperative binding of λ repressors to sites separated by integral turns of the DNA helix , 1986, Cell.

[37]  G. K. Ackers,et al.  Single-site mutations in the C-terminal domain of bacteriophage lambda cI repressor alter cooperative interactions between dimers adjacently bound to OR. , 1994, Biochemistry.

[38]  T Schlick,et al.  Dynamics of site juxtaposition in supercoiled DNA. , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[39]  M. A. Shea,et al.  Free energy coupling within macromolecules. The chemical work of ligand binding at the individual sites in co-operative systems. , 1983, Journal of molecular biology.

[40]  A. D. Kaiser,et al.  Control of lambda repressor synthesis. , 1971, Proceedings of the National Academy of Sciences of the United States of America.

[41]  Mark Ptashne,et al.  A Genetic Switch, Phage Lambda Revisited , 2004 .

[42]  S. Roy,et al.  Amino acid changes in the repressor of bacteriophage lambda due to temperature-sensitive mutations in its cI gene and the structure of a highly temperature-sensitive mutant repressor. , 1999, Protein engineering.

[43]  A. Sarai,et al.  Lambda repressor recognizes the approximately 2-fold symmetric half-operator sequences asymmetrically. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[44]  M Ptashne,et al.  Cooperative binding of lambda repressors to sites separated by integral turns of the DNA helix. , 1986, Cell.

[45]  D. Lewis Identification of promoters of Escherichia coli and phage in transcription section plasmid pSA850. , 2003, Methods in enzymology.

[46]  C. Pabo,et al.  Refined 1.8 A crystal structure of the lambda repressor-operator complex. , 1992, Journal of molecular biology.

[47]  A. Hochschild,et al.  Amino acid-amino acid contacts at the cooperativity interface of the bacteriophage lambda and P22 repressors. , 1998, Genes & development.

[48]  M Ptashne,et al.  Gene regulation at the right operator (OR) of bacteriophage lambda. II. OR1, OR2, and OR3: their roles in mediating the effects of repressor and cro. , 1980, Journal of molecular biology.

[49]  D. Dunlap,et al.  AFM studies of lambda repressor oligomers securing DNA loops. , 2009, Current pharmaceutical biotechnology.

[50]  B. Matthews,et al.  How Cro and lambda-repressor distinguish between operators: the structural basis underlying a genetic switch. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[51]  V. Zhurkin,et al.  "Antiparallel" DNA loop in gal repressosome visualized by atomic force microscopy. , 2003, Journal of molecular biology.

[52]  G. K. Ackers,et al.  Self-assembly of bacteriophage lambda cI repressor: effects of single-site mutations on the monomer-dimer equilibrium. , 1994, Biochemistry.

[53]  V. Pirrotta,et al.  Active Form of Two Coliphage Repressors , 1970, Nature.

[54]  M. Ptashne,et al.  Lambda repressor turns off transcription of its own gene. , 1975, Proceedings of the National Academy of Sciences of the United States of America.

[55]  G N Gussin,et al.  Characterization of a doubly mutant derivative of the lambda PRM promoter. Effects of mutations on activation of PRM. , 1988, Journal of molecular biology.

[56]  J. W. Little,et al.  Stability and Instability in the Lysogenic State of Phage Lambda , 2010, Journal of bacteriology.

[57]  F. Jacob,et al.  Regulation of repressor expression in lambda. , 1970, Proceedings of the National Academy of Sciences of the United States of America.

[58]  L. Beamer,et al.  Refined 1.8 p crystal structure of the ? repressor-operator complex*1 , 1992 .

[59]  L. Guarente,et al.  Mutant lambda phage repressor with a specific defect in its positive control function. , 1982, Proceedings of the National Academy of Sciences of the United States of America.

[60]  M. Ptashne,et al.  Sites of contact between λ operators and λ repressor , 1977 .

[61]  M. Ptashne,et al.  Gene regulation at the right operator (OR) of bacteriophage λ: III. λ Repressor directly activates gene transcription , 1980 .

[62]  M. Ptashne,et al.  DNA loops induced by cooperative binding of lambda repressor. , 1986, Nature.

[63]  M. Lewis,et al.  Crystal structure of the lambda repressor C-terminal domain provides a model for cooperative operator binding. , 2000, Cell.

[64]  M. A. Shea,et al.  The OR control system of bacteriophage lambda. A physical-chemical model for gene regulation. , 1985, Journal of molecular biology.

[65]  J. Keith Joung,et al.  Activation of prokaryotic transcription through arbitrary protein–protein contacts , 1997, Nature.

[66]  T. Itoh,et al.  Inhibition of ColE1 RNA primer formation by a plasmid-specified small RNA. , 1981, Proceedings of the National Academy of Sciences of the United States of America.

[67]  D. Dunlap,et al.  AFM studies of λ repressor oligomers securing DNA loops , 2009 .

[68]  K. Murakami,et al.  Identification of an UP element within the IHF binding site at the PL1-PL2 tandem promoter of bacteriophage lambda. , 1996, Journal of molecular biology.

[69]  A. Johnson,et al.  Interactions between DNA-bound repressors govern regulation by the lambda phage repressor. , 1979, Proceedings of the National Academy of Sciences of the United States of America.

[70]  J. W. Little,et al.  Autodigestion of lexA and phage lambda repressors. , 1984, Proceedings of the National Academy of Sciences of the United States of America.

[71]  Jordan,et al.  Structure of the lambda complex at 2.5 A resolution: details of the repressor-operator interactions , 1988, Science.

[72]  A. Sarai,et al.  Analysis of the sequence-specific interactions between Cro repressor and operator DNA by systematic base substitution experiments. , 1989, Proceedings of the National Academy of Sciences of the United States of America.