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Preface to the Third Edition | |
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Preface to the First Edition | |
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Introduction | |
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The Master Elements of Control | |
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Components of the Switch | |
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DNA | |
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RNA Polymerase | |
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The Repressor | |
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Cro | |
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The Action of Repressor and Cro | |
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Negative Control | |
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Positive Control | |
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Cooperativity of Repressor Binding | |
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Induction--Flipping the Switch | |
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Cooperativity--Switch Stability and Sensitivity | |
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The Effect of Autoregulation | |
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Other Cases | |
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Protein-DNA Interactions and Gene Control | |
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The Operator | |
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Repressor | |
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Cro | |
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Amino Acid-Base Pair Interactions | |
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The Promoter | |
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Gene Control | |
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Control Circuits--Setting the Switch | |
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A Brief Overview of [lambda] Growth | |
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The Genetic Map | |
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Circularization | |
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Gene Expression | |
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Integration | |
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Control of Transcription | |
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Very Early | |
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Early | |
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Late Lytic | |
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Late Lysogenic | |
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The Decision | |
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Control of Integration and Excision | |
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Establishing Lysogeny | |
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Lytic Growth | |
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Induction | |
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Other Phages | |
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The SOS Response | |
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[lambda] Pathways and Cell Development | |
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Regulatory Genes | |
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Switches | |
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Patterns of Gene Expression | |
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How Do We Know--the Key Experiments | |
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The Repressor Idea | |
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Clear and Virulent Mutants | |
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Observations | |
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Explanation | |
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Immunity and Heteroimmunity | |
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Observations | |
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Explanation | |
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Asymmetry in Bacterial Mating | |
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Observations | |
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Explanation | |
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The Repressor Problem in the Early 1960s | |
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Repressor Isolation and DNA Binding | |
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Making More Repressor | |
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The Claims of Chapters One and Two | |
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The repressor is composed of two globular domains held together by a linker of some 40 amino acids | |
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The repressor dimerizes, largely through interaction between its carboxyl domains | |
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A repressor dimer binds, through its amino domains, to a 17 base pair operator site | |
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A single operator site binds one dimer of repressor | |
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Dimers form before DNA binding | |
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The amino domains contact DNA | |
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There are three 17 base pair repressor binding sites in the right operator. At each site repressor and Cro bind along the same face of the helix | |
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Chemical probes | |
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Operator mutations | |
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Binding to supercoiled and linear DNA | |
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Repressor binds to three sites in O[subscript R] with alternate pairwise cooperativity. The cooperativity is mediated by interactions between carboxyl domains of adjacent dimers | |
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In a lysogen repressor is typically bound to O[subscript R]1 and O[subscript R]2. The bound repressors turn off rightward transcription of cro and stimulate leftward transcription of cl. At higher concentrations, repressor binds to O[subscript R]3 to turn off transcription of cl | |
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Cro binds first to O[subscript R]3, then to O[subscript R]1 and O[subscript R]2, thereby first turning off P[subscript RM], then P[subscript R] | |
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Some background about Cro | |
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Cro in vivo | |
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Cro in vitro | |
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RecA cleaves repressor to trigger induction | |
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When Cro is bound at O[subscript R]3 the switch is thrown | |
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Repressor and Cro bind to the operator as shown in Figures 2.6, 2.8, 2.10, and 2.11 | |
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Crystallography | |
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The "helix swap" experiment | |
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Specific amino acid-base pair contacts | |
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The role of the arm of [lambda] repressor | |
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Repressor activates transcription of cl by binding to O[subscript R]2 and contacting polymerase with its amino domain | |
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Positive control mutants | |
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Positive control in vitro | |
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Conclusion | |
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2004: New Developments | |
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Long-range Cooperativity and Repression of P[subscript RM] | |
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An Octamer of Repressor Binds O[subscript R] and O[subscript L] | |
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Autonegative Regulation of Repressor Synthesis | |
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How Do We Know | |
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Long-range Interactions and Repression of P[subscript R] | |
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Long-range Interactions and Repression of P[subscript RM] | |
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Activation and Repression of P[subscript RM] | |
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Repressor Structure | |
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Positive Control (Activation of Transcription) | |
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Polymerase and Promoter | |
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The Mechanism of Activation | |
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How Do We Know | |
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Activating Region Variants | |
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A Suppressor of a pc Mutant | |
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Crystallography | |
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Activator Bypass | |
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Changing Activating Regions and Target Context | |
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The Structure of the Repressor Monomer and the Mechanism of Repressor Cleavage | |
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How Do We Know | |
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Evolving the Switch | |
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Changing the Affinities of Sites in O[subscript R] for Repressor | |
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Eliminating Positive Control | |
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Eliminating Cooperativity between DNA-binding Dimers | |
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CII and the Decision | |
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Index | |