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Genome-wide Functional Linkage Maps Methods for inferring functional linkages: Complexes, Pathways Rosetta stone Phylogenetic profiles Gene neighbors Operon method (Microarray method) The Genome-wide functional linkage Map in M. tb Assessing accuracy of functional linkages Functional linkages in structural genomics Analyzing parallel pathways The DIP and ProLinks databases
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Diphtheria Toxin Dimer vs. Monomer Bennett et al., PNAS, Vol. 91, 3127-3131 (1994)
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Marcotte et al. (1999) Science, 285, 751
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PHYLOGENETIC PROFILE METHOD Pellegrini et al (1999) PNAS 96, 4285
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The Gene Neighbor Method for Inferring Functional Linkages genome 1... genome 2genome 3 genome 4 A A A A B B B B C C C C A B C A statistically significant correlation is observed between the positions of proteins A and B across multiple genomes. A functional relationship is inferred between proteins A and B, but not between the other pairs of proteins:
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gene Abbbb gene B gene C OPERON or GENE CLUSTER method of inferring functional linkages in the genome of Mycobacterium tuberculosis The 100 bp threshold is chosen because it gives the broadest coverage consistent with high accuracy Research of Michael Strong
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vs Network Interaction Map vs. Genome-Wide Functional Linkage Map Strong, Graeber et al. (2003) Nucleic Acid Research, 31, 7099
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Figure 7. M. Strong, T. Graeber et al.
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Requiring 2 or more functional linkages: 1,865 genes make 9,766 linkages
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A E F C B D
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A E F C B D Cluster A: 6 genes; 5 annotated 4 linkages 5 genes coding for DNA replication or repair The 6 th gene inferred to be involved in DNA binding, and in fact encodes a Zn-ribbon
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A E F C B D Cluster A: 6 genes; 5 annotated 5 linkages 5 genes coding for DNA replication or repair The 6 th gene inferred to be involved in DNA binding, and in fact encodes a Zn-ribbon None of the genes is a homolog
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A E F C B D Cluster B: 6 genes; 7 linkages 3 genes: Ser/Thr kinase or phophatase activities 2 genes: cell wall biosynth. 1 gene: unannotated Gene 14, pknB (a Ser/Thr kinase) contains PASTA domains (penicillin-binding serine/threonine kinase associated)
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A E F C B D Cluster B: 6 genes; 7 linkages 3 genes: Ser/Thr kinase or phophotase activities 2 genes: cell wall biosynth. 1 gene: unannotated Gene 19 is unannotated. It contains A FHA (Forkhead associated) domain, which binds phosphothreonine containing proteins.
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A E F C B D Cluster D: Links gene 50 (a penicillin binding protein involved in cell wall synthesis) to gene 51 (an integral membrane protein).
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A E F C B D E is a functional link between gene 16 (pbkA in cell wall biosynthesis) and gene 50 (the penicillin binding protein involved in cell wall biosynthesis)
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Some columns show similar linkages, so cluster like columns, using Eisen et al.(1998) procedure, CLUSTER
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Hierarchical clustering of the TB Whole Genome Functional Linkage Map Research of Michael Strong and Tom Graeber Functional modules range in size From 2 to > 100 linkages Dozens of off diagonal functional linkages
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Detoxification Polyketide and non-ribosomal Peptide synthesis Energy Metabolism, oxidoreductases Polyketide and non- ribosomal,Degradation of Fatty acids, and Energy Metabolism Degradation of Fatty acids Research of Michael Strong and Tom Graeber
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Detoxification Polyketide and non-ribosomal peptide synthesis Energy Metabolism, oxidoreductase Deg. of Fatty Acids Virulence Energy Metabolism, oxidoreductase Amino acid Biosynthesis Emergy Metab. Respiration Aerobic Lipid Biosynthesis Degradation of Fatty Acids Amino Acid Biosynthesis (Branched) Synthesis and Modif. Of Macromolecules, rpl,rpm, rps Biosynthesis of Cofactors, Prosthetic groups Purine, Pyrimidine nucleotide biosynthesis Novel Group Sugar Metabolism Aromatic Amino Acid Biosynthesis Energy Metabolism, Anaerobic Respiration Two component systemsCell Envelope Cytochrome P450Chaperones Biosynthesis of cofactors Cell Envelope, Cell Division Transport/Binding Proteins Energy Metabolism TCA Broad Regulatory, Serine Threonine Protein Kinase Cell Envelope, Murein Sacculus and Peptidoglycan Transport/Binding Proteins Cations Energy Metabolism, ATP Proton Motive force Fig 4. M. Strong, T. Graeber et al.
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Detoxification Polyketide and non-ribosomal peptide synthesis Energy Metabolism, oxidoreductase Deg. of Fatty Acids Virulence Energy Metabolism, oxidoreductase Amino acid Biosynthesis Emergy Metab. Respiration Aerobic Lipid Biosynthesis Degradation of Fatty Acids Amino Acid Biosynthesis (Branched) Biosynthesis of Cofactors, Prosthetic groups Purine, Pyrimidine nucleotide biosynthesis Novel Group Sugar Metabolism Aromatic Amino Acid Biosynthesis Energy Metabolism, Anaerobic Respiration Two component systemsCell Envelope Cytochrome P450Chaperones Biosynthesis of cofactors Cell Envelope, Cell Division Transport/Binding Proteins Energy Metabolism TCA Broad Regulatory, Serine Threonine Protein Kinase Cell Envelope, Murein Sacculus and Peptidoglycan Transport/Binding Proteins Cations Energy Metabolism, ATP Proton Motive force One of 7 modules of unannotated linkages, perhaps undiscovered pathways or complexes
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HisG HisF HisI / HisI2 HisA HisH HisB HisC / HisC2 HisB HisD Pathway Reconstruction from Functional Linkages All 9 enzymes of the histidine biosynthesis pathway are linked, and are clustered separately from other amino acid synthetic pathways
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CtaD CtaECtaC Functional Linkages Among Cytochrome Oxidase Genes CtaB Functional linkages relate all 3 components of cytochrome oxidase complex and also CtaB, the cytochrome oxidase assembly factor These genes are at four different chromosomal locations Membrane proteins linked to soluble proteins
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Quantitative Assessment of Inferred Protein Complexes Research of Edward Marcotte, Matteo Pellegrini, Michael Thompson and Todd Yeates
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Calculating Probabilities of Co- evolution Phylogenetic Profile Rosetta Stone Gene Neighbor Operon N= number of fully sequenced genomes n= number of homologs of protein A m = number of homologs of protein B k = number of genomes shared in common X= fractional separation of genes n = intergenic separation
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Combining Inferences of Co- Evolution from 4 Methods We use a Bayesian approach to combine the probabilities from the four methods to arrive at a single probability that two proteins co-evolve: where positive pairs are proteins with common pathway annotation and negative pairs are proteins with different annotation
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ProLinks Database www.dip.doembi.ucla.edu/pronav ~ 10,000,000 Functional Linkages inferred from 83 fully sequenced genomes
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Benchmarking this Approach Against Known Complexes Ecocyc: Karp et al. NAR, 30, 56 (2002) True positive interactions are between subunits of known complexes and false positive ones are between subunits of different complexes. For high confidence links, we find 1/3 of true interactions with only one 1/1000 of the false positive ones Random Research of Matteo Pellegrini
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Benchmarking our Approach Against Known Complexes True positive interactions are between subunits of known complexes and false positive ones are between subunits of different complexes. For the first few hundred pairs of high confidence links, about 50% are between subunits of known complexes
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Example Complex: NADH Dehydrogenase I 11 of 13 subunits detected
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Example Complex: NADH Dehydrogenase I 11 of 13 subunits detected 3 false positives
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From Inferred Protein Linkages to Structures of Complexes Research of Michael Strong, Shuishu Wang, Markus Kauffman
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PE, PE-PGRS, and PPE Proteins in M. tuberculosis 38 PE proteins; 61 PE-PGRS proteins; 68 PPE proteins Together compromise about 5 % of the genome No function is known, but some appear to be membrane bound No structure is known: always insoluble when expressed Goal: use functional linkages to predict a complex between a PE and a PPE protein: express complex, and determine its structure Research of Shuishu Wang and Michael Strong The Problem of PE and PPE Proteins in M. tb
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Construction of a co-expression vector to test for protein-protein interactions (Mike Strong) pET 29b(+) T7 promoter lac oper. RBS Nde1 HindIIIKpn1NcoI RBS gene A gene B Thrombin site His tag polycistronic mRNA transcription translation protein A protein B (with His tag) If proteins interact (protein-protein interaction) If proteins do not interact
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When co-expressed, the PE and PPE proteins, inferred to interact, do form a soluble complex, Mr = 35,200 Sedimentation equilibrium experiments: Rv2430c + Rv2431c fraction 49, in 20mM HEPES, 150mM NaCl, pH 7.8 Concentration OD 280 0.7, 0.45, 0.15 Expected Mr: Rv 2431c (PE) 10,687 (10563.12 from Mass Spec) Rv2430c+His tag (PPE) 24,072 (23895.00 from Mass Spec) Possibly suggests a 1:1 complex between these two proteins
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Crystallization trials of the Complex Between PE Protein Rv2430c and PPE Protein Rv2431c
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Database of Interacting Proteins www.dip.doe-mbi.ucla.edu Experimentally detected interactions from the scientific literature Currently ~ 44,000 interactions
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The DIP Database DOE-MBI LSBMM, UCLA
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* * * Live DIP Gives the States of Proteins Transitions Documented
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ProLinks Database and the Protein Navigator Contains some 10,000,000 inferred functional linkages from 83 genomes Available at www.doe-mbi.ucla.eduwww.doe-mbi.ucla.edu Soon to be expanded to 250 fully sequenced genomes Eventually to be reconciled with DIP
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Summary A X Y Z B V C A protein’s function is defined by the cellular context of its linkages Many functional linkages are revealed from genomic and microarray data (high coverage) Validity of functional linkages can be assessed by compar- ison to known complexes, and to expression data, and by keyword recovery Clustered genome-wide functional maps can reveal and organize information on complexes and pathways Functional linkages can reveal protein complexes suitable for structural studies
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Protein Interactions Analysis of M.tb. Genome Michael Strong Whole Genome Interaction Maps Michael Strong & Tom Graeber Methods of Inferring Interactions Edward Marcotte, Matteo Pellegrini, Todd Yeates Michael Thompson, Richard Llwellyn Database of Interacting Proteins Lukasz Salwinski, Joyce Duan, Ioannis Xenarios, Robert Riley, Christopher Miller Parallel pathways Huiying Li
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