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Methods and resources for pathway analysis

Methods and resources for pathway analysis. PABIO590B Week 2. Pathways overview. Introduction to pathways and networks Examples of pathways and networks Review of pathway databases and tools Representing pathways and networks Methods of inferring pathways and networks

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Methods and resources for pathway analysis

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  1. Methods and resources for pathway analysis PABIO590BWeek 2

  2. Pathways overview • Introduction to pathways and networks • Examples of pathways and networks • Review of pathway databases and tools • Representing pathways and networks • Methods of inferring pathways and networks • Pathway and cellular simulations

  3. Pathways vs. networks Gene networks • Clusters of genes (or gene products) with evidence of co-expression • Connections usually represent degrees of co-expression • In-depth knowledge of process is not necessary • Networks are non-predictive Biochemical pathways • Series of chained, chemical reactions • Connections represent describable (and quantifiable) relations between molecules, proteins, lipids, etc. • Enzymatic process is elucidated • Changes via perturbation are predictable downstream

  4. Pathways vs. networks

  5. Pathway and network granularity Curated reaction pathways Qualitative networks Effort to curate Mathematical simulation models Probabilistic networks General interaction networks Level of detail

  6. Introduction to pathways and networks • Examples of pathways and networks • Review of pathway databases and tools • Representing pathways and networks • Methods of inferring pathways and networks • Pathway and cellular simulations

  7. Yeast gene interaction network Tong, et al., Science 303, 808 (2004)

  8. Characteristics of the yeast gene network • Some genes (e.g. regulatory factors) act as ‘hubs’ in a network and have many interactions • Degrees of connectivity follows the power law • Hubs may make interesting anti-cancer targets • Clusters of genes with known function suggest function for hypothetical genes in same cluster • Network characteristics can be used to predict protein-protein interactions • Path between two genes tends to be short (average ~3.3 hops) Tong, et al., Science 303, 808 (2004)

  9. E. coli metabolic pathway glycolysis Karp, et al., Science 293, 2040 (2001)

  10. Pathways: E. coli metabolic map • Encompasses >791 chemical compounds in >744 noted biochemical reactions • Pathway was compiled via literature information extraction and extensive manual curation • System allows for users to indicate evidence of pathway annotations • Curation is done collaboratively with numerous experts outside of EcoCyc Karp, et al., Science 293, 2040 (2001)

  11. Pathways in bioinformatics • Most resources for pathways focus on metabolic pathways (signaling and regulatory gaining prominence) • Pathways as a very specific subtype of networks • Like networks, can be made in computable (symbolic) form • Specificities in chemical reactions are more predictive • Pathways can chain together, forming larger pathways Karp, et al., Science 293, 2040 (2001)

  12. Introduction to pathways and networks • Examples of pathways and networks • Review of pathway databases and tools • Representing pathways and networks • Methods of inferring pathways and networks • Pathway and cellular simulations

  13. Pathway repositories • BioCyc/MetaCyc • Kyoto Encyclopedia of Genes and Genomes (KEGG) PATHWAY DB • BioCarta • BioModels database

  14. BioCyc databasehttp://www.biocyc.org • Pathway/genome database (PGDB) for organisms with completely sequenced genomes • 409 full genomes and pathways deposited • Species-specific pathways are inferred form MetaCyc • Query/navigation/pathway creation support through the Pathway Tools software suite

  15. http://www.biocyc.org

  16. MetaCyc database http://www.metacyc.org • Non-redundant reference database for metabolic pathways, reactions, enzymes and compounds • Curation through experimental verification and manual literature review • >1200 pathways from 1600+ species (mostly plants and microorganisms)

  17. http://www.metacyc.org

  18. Glycolysis pathway in MetaCyc http://www.metacyc.org

  19. KEGG PATHWAY databasehttp://www.kegg.com • Consolidated set of databases that cover genomics (GENE), chemical compounds (LIGAND) and reaction networks (PATHWAY) • Broad focus on metabolics, signal transduction, disease, etc. • Species-specific views available (but networks are static across all organisms)

  20. http://www.kegg.com

  21. Glycolysis pathway in KEGG http://www.kegg.com

  22. Global Pathway Map

  23. BioCarta databasehttp://www.biocarta.com • Corporate-owned, publicly-curated pathway database • Series of interactive, “cartoon” pathway maps • Predominantly human and mouse pathways • Contains 120,000 gene entries and 355 pathways

  24. http://www.biocarta.com

  25. Glycolysis pathway in BioCarta http://www.biocarta.com

  26. BioModels databasehttp://www.biomodels.net • Database for published, quantitative models of biochemical processes • All models/pathways curated manually, compliant with MIRIAM • Models can be output in SBML format for quantitative modeling • 86 curated models, 40 models pending curation

  27. http://www.biomodels.net

  28. Glycolysis pathways in BioModels http://www.biomodels.net

  29. Comparison of pathway databases

  30. Introduction to pathways and networks • Examples of pathways and networks • Review of pathway databases and tools • Representing pathways and networks • Methods of inferring pathways and networks • Pathway and cellular simulations

  31. Pathway formats • Extensible Markup Language (XML) • Systems Biology Markup Language (SBML) • BioPax

  32. Extensible Markup Language (XML) • Standard of representing information in a machine-readable way • Similar to HTML; tags can enclose or contain data <myXMLData> <someTag>Some data here</someTag> <anotherTag>More stuff here</anotherTag> <attributeTag data=“embedded in tag” /> </myXMLData>

  33. Systems Biology Markup Language • XML-based language for representing biochemical reactions • Oriented towards software data-sharing • Tiered, upward-compatible architecture (two, upward-compatible levels, third planned) • Primary intended use is for quantitative model simulations

  34. SBML

  35. BioPax • Like SBML, XML-based pathway representation • Tiered structure • Level 1: Metabolic pathway information • Level 2: Level 1 + Molecular interaction, post-translational modification • Intended to be a lingua franca for pathway databases

  36. BioPax XML representation

  37. Introduction to pathways and networks • Examples of pathways and networks • Review of pathway databases and tools • Representing pathways and networks • Methods of inferring pathways and networks • Pathway and cellular simulations

  38. Inferring pathways and networks • Experimental methods • Microarray co-expression • Quantitative trait locus mapping (QTL) • Isotope-coded affinity tagging (ICAT) • Yeast two-hybrid assay • Green florescent protein tagging (GFP tagging) • Computational methods • Database-driven protein-protein interactions • Expression clustering techniques • Literature-mining for specified interactions

  39. Introduction to pathways and networks • Examples of pathways and networks • Review of pathway databases and tools • Representing pathways and networks • Methods of inferring pathways and networks • Pathway and cellular simulations

  40. Cellular simulations • Study the effect perturbation has on a pathway (and thus the organism) • Generally require extensive detail on the pathway or reactions of interest (flux equations, metabolite concentration, etc.) • Cellular pathway simulations must manage both temporal and spatial complexity

  41. organs and organisms picosec. nanosec. microsec. millisec. sec. min. yr. Temporal intervals systems physiology cellular processes molecular dynamics quantummechanics 0.1 nm 10nm 1um 1mm 1cm 1m Spatial dimension Adapted from Kelly, H., http://www.fas.org/resource/05242004121456.pdf , via Neal, Yngve 2006 VHS, UW MEBI 591

  42. Simulation methods and techniques Adapted from Tomita 2001

  43. Research in simulation and modeling • Virtual Cell (National Resource for Cell Analysis and Modeling) • MCell (the Salk Institute) • Gepasi (Virginia Tech) • E-CELL (Institute for Advanced Biosciences, Keio University) • Karyote/CellX (Indiana University)

  44. Your task is to: Exercise • Identify the functions of proteins X, Y & Z • Identify the pathway(s) in which they are involved • Look for differences in pathways between databases • Examine the same pathway(s) in humans

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