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MCB 317 Genetics and Genomics Topic 11, part 2 Genomics Slide 2 Need to Add to part 2 or 3 A.Chip-seq B.Deep sequencing for expression profiling C.Illumina? movie Slide 3 Genomics Summary A.Microarrays: expression profiling and other uses B.Global Gene Knockouts C.Global protein localization in yeast D.Global complex identification in yeast E.Global two-hybrid analysis in yeast and other organisms F.RNAi G.Transgenics, gene knock-outs (genetics not genomics) H.Human Genome Project, Next Generation Sequencing, and Comparative Genomics Slide 4 Yeast Knockout Library Delete YFG Delete all genes (individually) Slide 5 Disruption of All Yeast Genes Approx 6000 genes Make 6000 sets of disruption primers Disrupt each gene in a diploid Dissect all 6000 diploids Identify set of essential genes Identify set of non-essential genes Slide 6 Yeast Knockout Library Delete one copy of each gene in diploid 5,916 genes deleted 5,916 diploid strains constructed Dissect to determine if gene is essential 1,105 genes = essential 18.7% of genes = essential Construct an ordered library of haploids for non- essential genes 4,811 mutant strains in library Slide 7 Genomics Summary A.Microarrays: expression profiling and other uses B.Global Gene Knockouts C.Global protein localization in yeast D.Global complex identification in yeast E.Global two-hybrid analysis in yeast and other organisms F.RNAi G.Transgenics, gene knock-outs (genetics not genomics) H.Human Genome Project, Next Generation Sequencing, and Comparative Genomics Slide 8 Ab Protein Txn Profile Gene Orthologs and Paralogs Mutant Gene Biochemistry Genetics Mutant Organism A C F Subunits of Protein Complex B, G D E Protein Profile/ Localization Genomics: High-throughput genetics Genomics B, G H Slide 9 Slide 10 Slide 11 Slide 12 Genomics Summary A.Microarrays: expression profiling (and other uses) B.Global Gene Knockouts C.Global protein localization in yeast D.Global complex identification in yeast E.Global two-hybrid analysis in yeast and other organisms F.RNAi G.Transgenics, gene knock-outs (genetics not genomics) H.Human Genome Project, Next Generation Sequencing, and Comparative Genomics Slide 13 Ab Protein Txn Profile Gene Orthologs and Paralogs Mutant Gene Biochemistry Genetics Mutant Organism A C F Subunits of Protein Complex B, G D E Protein Profile/ Localization Genomics: High-throughput genetics Genomics B, G H Slide 14 Slide 15 Slide 16 Slide 17 Genomics Summary A.Microarrays: expression profiling and other uses B.Global Gene Knockouts C.Global protein localization in yeast D.Global complex identification in yeast E.Global two-hybrid analysis in yeast and other organisms F.RNAi G.Transgenics, gene knock-outs (genetics not genomics) H.Human Genome Project, Next Generation Sequencing, and Comparative Genomics Slide 18 Ab Protein Txn Profile Gene Orthologs and Paralogs Mutant Gene Biochemistry Genetics Mutant Organism A C F Subunits of Protein Complex B, G D E Protein Profile/ Localization Genomics:Hi gh- throughput genetics Genomics B, G H Slide 19 Slide 20 8100 Human DBD-ORFs x 8100 Human AD-ORFs Slide 21 Slide 22 Genomics Summary A.Microarrays: expression profiling and other uses B.Global Gene Knockouts C.Global protein localization in yeast D.Global complex identification in yeast E.Global two-hybrid analysis in yeast and other organisms F.RNAi G.Transgenics, gene knock-outs (genetics not genomics) H.Human Genome Project, Next Generation Sequencing, and Comparative Genomics Slide 23 Evolution of RNAi (current model) 1.a. Viruses are bad (so are transposons). b. Many viruses have dsRNA genomes c. euks originally lacked dsRNAs d. invent mechanism to kill dsRNA 2. Evolve mechanism to regulate endogenous genes a. RNA degradation b. inhibit translation c. form heterochromatin 3. Use as experimental technique Slide 24 Genomics Summary A.Microarrays: expression profiling and other uses B.Global Gene Knockouts C.Global protein localization in yeast D.Global complex identification in yeast E.Global two-hybrid analysis in yeast and other organisms F.RNAi G.Transgenics, gene knock-outs (genetics not genomics) H.Human Genome Project, Next Generation Sequencing, and Comparative Genomics Slide 25 Knockout Mouse: The Goal YFG Replace the coding region of YFG with a selectable marker gene Marker Gene Slide 26 Knockout Mouse Transfected DNA can integrate at random sites (standard transgenic organism). This is a relatively common event. Or the Transfected DNA can Replace the Endogenous Copy of the Gene via Homologous Recombination. This is a relatively rare event. Slide 27 Gene Deletion Deletion by Homologous Recombination Marker Gene Slide 28 Knockout Mouse Slide 29 How to select for the cells in which the Occludin gene is replaced with a mutant allele (a null allele) in the face of the fact that most of the transformed DNA will integrate at random sites? neo r gene makes mammalian cells resistance to the drug G418 tk NSV makes mammalian cells sensitive to the drug ganciclovir Slide 30 Knockout Mouse YFG Red = Mouse DNA including YFG and regions upstream and downstream of YFG Blue = neor gene, Green = tkHSV gene Black = plasmid DNA (not homologous to any mouse DNA) neo r tk HSV Slide 31 Knockout Mouse Lodish 5-40 Slide 32 Knockout Mouse Slide 33 Different Types of Transgenic Organisms Slide 34 Genomics Summary A.Microarrays: expression profiling and other uses B.Global Gene Knockouts C.Global protein localization in yeast D.Global complex identification in yeast E.Global two-hybrid analysis in yeast and other organisms F.RNAi G.Transgenics, gene knock-outs (genetics not genomics) H.Human Genome Project, Next Generation Sequencing, and Comparative Genomics Slide 35 Goals of Human Genome Project 1.Generate Genetic, Physical and Sequence maps of the human genome 2.Sequence genomes of a variety of model organisms: Comparative Genomics 3.Develop improved technology for mapping and sequencing 4.Develop computational tools for capturing, storing, analyzing, displaying, and distributing map and sequence data 5.Sequence ESTs and cDNAs 6.Consider social, ethical and legal challenges posed by genetic information Slide 36 Genomicists look at two basic features of genomes: sequence and polymorphism Major challenges to determine sequence of each chromosome in genome and identify many polymorphisms How does one sequence a 500 Mb chromosome 600 bp at a time? How accurate should a genome sequence be? DNA sequencing error rate is about 1 per 600 bp How does one distinguish sequence errors from polymorphisms? Rate of polymorphism in diploid human genome is about 1 in 1000 bp Repeat sequences may be hard to place Unclonable DNA cannot be sequenced Up to 30% of genome is heterochromatic DNA that can not be cloned Slide 37 Whole-genome shotgun sequencing Private company Celera used to sequence whole human genome Whole genome randomly sheared three times Plasmid library constructed with ~ 2kb inserts Plasmid library with ~10 kb inserts BAC library with ~ 200 kb inserts Computer program assembles sequences into chromosomes No physical map construction Only one BAC library Overcomes problems of repeat sequences Fig. 10.13 Slide 38 Pyrosequencing, pt 1 Rxn2 Adenosine phosphosulfate = APS APS + PP i ATP Rxn1 (DNA) n + dNTP (DNA) n+1 + PP i ATP sulfurylase DNAP Slide 39 Pyrosequencing, pt 2 Luciferin Luciferase Oxyuciferin + Light ATPADP Apyrase: dNTP -> dNDP + Pi -> dNMP + Pi + Pi Slide 40 Pyrosequencing, overview GCTACACT CGATGTGACTGTA dTTP PP i APS ATP Luciferin Luciferase Oxyuciferin + Light Slide 41 Pyrosequencing Add one nt (A) -> detect light (yes or no) Apyrase degrades excess nt (A) Add next nt (C) -> detect light (yes or no) Apyrase degrades excess nt (C) Repeat cycle 100s of times Slide 42 Pyrosequencing Slide 43 Emulsion PCR 1. Add linkers (primers) to ends of genomic fragments 2. Attach frags to 1000s of beads in a mixture 3. Add PCR reagents 4. Add oil and make an emulsion so that each bead is in its own droplet (its own PCR reaction) 5. Amplify DNA to make millions of identical copies. Each bead has millions of copies of a single DNA Slide 44 Pyrosequencing Pico-titer plate 200,000-400,000 wells per plate 1. Add beads to picotiter plate, only one bead fits in each well 2. Add a second type of bead, smaller, that holds the DNA bead in the wells and delivers enzymes to the wells 3. Flow the nts into the wells one at a time and record the light emitted from each well using a CCD camera Slide 45 Pyrosequencing Currently the best machines can sequence 400 - 600 million base pairs in one 10 hour run Haploid human genome = 3,000,000,000 bp therefore sequence haploid human genome to 1x depth in 6 days with one machine. The current target goal for sequencing individual human genomes is to get the cost down to $1,000 per genome. At present the cost is around $5,000-$10,000 per individual (last year) Illumina claims to have hit the $1,000 cost per genome in January of 2014 Slide 46 Illumina Sequencing Technology See Movie