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MCB 317 Genetics and Genomics MCB 317 Topic 10, part 4 A Story of Transcription
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Deletion and Linker Scanner Analysis In vitro Txn Assay Promoter sufficient in vitro Identification of Enhancers Identify and define TBP and basal factors Extract + Prom.-Enh. Basal Facts. + Prom.-Enh. Activated Txn (Enhanced) & Regulated Txn Extract + Prom.-Enh. Activators Co-activators + Enhancer & TBP & TAFs Promoter “Activated” txn & Regulated txn In vivo Txn Assay Promoter not Sufficient
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Co-activators and Chromatin Remodeling Complexes
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Co-activators & chromatin remodeling complexes not shown
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How could we have missed Co-activators and Chromatin Remodelling Complexes for 20+ years? How to study what’s going on and what’s important in vivo?
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Purify Polymerases Immuno-affinity Purification, Mass Spec Mediator In vitro “chromatin” Assembly Genetic Screens In vitro txn of in vitro “chromatin” Coactivators Chromatin Remodeling Complexes “Histone” Biochemistry Activators
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Strength of Genetics as a Tool Strength of Genetics: Is a Gene Important in vivo? Limitation of biochemistry: Does an in vitro assay recapitulate the entire in vivo process?
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Concept: Comprehensive view of a molecular process requires both Genetics and Biochemistry
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Genetic Screens (Yeast mostly) Coactivators Chromatin Remodeling Complexes Basal Factors Activators Mediator RNAP II
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Purify Polymerases Immuno-affinity Purification, Mass Spec Mediator In vitro “chromatin” Assembly Genetic Screens In vitro txn of in vitro “chromatin” Coactivators Chromatin Remodeling Complexes “Histone” Biochemistry Activators
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Coding RegionPrUAS Enzyme involved in sucrose metabolism
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Coding RegionPrUAS Enzyme involved in sucrose metabolism
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Genetic Screens: Primary screen and initial characterization of mutants 1. Screen for mutants 2. Phenotype due to a single mutation? 3. Dominant or Recessive? 4. Complementation tests
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Our snf- screen = many complementation groups = many genes snf1 snf2 snf3 snf4 snf5 snf6 snf7 snf8….. Which, if any encode txn factors? Secondary screen to identify possible txn factors
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Genetic Screens: Primary screen Secondary screen(s)
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SUC2 encodes an enzyme that metabolizes sucrose. SUC2 txn is induced in response to sucrose Transform Reporter into each of our mutant strains: snf1-, snf2-, snf3-, snf4-, snf5-, snf6-, etc. Three key complementation groups identified: SNF2, SNF5 and GCN5
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Raise antibodies to Snf2 and Snf5 proteins and use them to purify the native proteins from wild-type yeast cells Snf2 and Snf5 are part of the same large protein complex
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Nuclease Protection Assay = variation on footprinting that provides information on where histones bind and on which bases and strands of the DNA faces outward on the nucleosome surface and which face inward
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Purify Polymerases Immuno-affinity Purification, Mass Spec Mediator In vitro “chromatin” Assembly Genetic Screens In vitro txn of in vitro “chromatin” Coactivators Chromatin Remodeling Complexes “Histone” Biochemistry Activators
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Back to GCN5
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Continuing Concept: Comprehensive view of a molecular process requires both Genetics and Biochemistry
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Histone Modification Histone Code
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Lodish 11-32 UAS = Upstream Activation Site = Yeast Enhancer Gcn4 is an Activator Gcn5 is a subunit of a co-activator (SAGA) that has histone acetylase activity
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Activators One function of activators is to act as a “platform” that recruits (binds) Co-activators
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Purify Polymerases Immuno-affinity Purification, Mass Spec Mediator In vitro “chromatin” Assembly Genetic Screens In vitro txn of in vitro “chromatin” Coactivators Chromatin Remodeling Complexes “Histone” Biochemistry Activators
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How could we have missed Co-activators and Chromatin Remodelling Complexes for 20+ years? How to study what’s going on and what’s important in vivo?
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Purify Polymerases Immuno-affinity Purification, Mass Spec Mediator In vitro “chromatin” Assembly Genetic Screens In vitro txn of in vitro “chromatin” Coactivators Chromatin Remodeling Complexes “Histone” Biochemistry Activators
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