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Introduction to the Gene Ontology and GO Annotation Resources EBI Bioinformatics Roadshow 13th June 2012 Rotterdam, Netherlands Duncan Legge EBI is an Outstation of the European Molecular Biology Laboratory. OUTLINE OF TUTORIAL: PART I: Ontologies and the Gene Ontology (GO) PART II: GO Annotations How to access GO annotations How scientists use GO annotations PART I: Gene Ontology What does an ontology provide? 1. Consistent terminology – controlled vocabulary. 2. Relationships between terms – hierarchy. Controlled vocabulary Q: What is a cell? A: It really depends who you ask! Different things can be described by the same name The same thing can be described by different names: • • • • • Glucose synthesis Glucose biosynthesis Glucose formation Glucose anabolism Gluconeogenesis Inconsistency in naming of biological concepts • Same name for different concepts • Different names for the same concept Comparison is difficult – in particular across species or across databases Just one reason why the Gene Ontology (GO) is is needed… Why do we need GO? • Inconsistency in naming of biological concepts • Large datasets need to be interpreted quickly •Increasing amounts of biological data available • Increasing amounts of biological data to come Increasing amounts of biological data available Search on mesoderm development…. you get 9441 results! Expansion of sequence information 1700s 1606 What is an ontology? • Dictionary: • A branch of metaphysics concerned with the nature and relations of being (philosophy) • A formal representation of the knowledge by a set of concepts within a domain and the relationships between those concepts (computer science) • Barry Smith: • The science of what is, of the kinds and structures of objects, properties, events, processes and relations in every area of reality. What is an ontology? • More usefully: • An ontology is the representation of something we know about. “Ontologies" consist of a representation of things, that are detectable or directly observable, and the relationships between those things. What’s in an Ontology? What is the Gene Ontology (GO)? A way to capture biological knowledge in a written and computable form Describes attributes of gene products (RNA and protein) E. Coli hub http://www.geneontology.org Reactome The scope of GO What information might we want to capture about a gene product? • What does the gene product do? • Where does it act? • How does it act? Biological Process what does a gene product do? A commonly recognised series of events transcription cell division Cellular Component where is a gene product located? • plasma membrane • mitochondrion • mitochondrial membrane • mitochondrial matrix • mitochondrial lumen • ribosome • large ribosomal subunit • small ribosomal subunit Molecular Function how does a gene product act? • • insulin binding • insulin receptor activity glucose-6-phosphate isomerase activity Three separate ontologies or one large one? • GO was originally three completely independent hierarchies, with no relationships between them • As of 2009, GO have started making relationships between biological process and molecular function in the live ontology Process Function art of Function sa • GO IS: • species independent • covers normal processes • GO is NOT: • NO pathological/disease processes • NO experimental conditions • NO evolutionary relationships • NOT a nomenclature system Aims of the GO project • Edit the ontologies • Annotate gene products using ontology terms • Provide a public resource of data and tools Anatomy of a GO term Unique identifier Term name Definition Synonyms Crossreferences Ontology structure Less specific node • Nodes = terms in the ontology node More specific node edge • Edges = relationships between the concepts node • GO is structured as a hierarchical directed acyclic graph (DAG) • Terms can have more than one parent and zero, one or more children • Terms are linked by reationships, which add to the meaning of the term Relationships between GO terms • is_a • part_of • regulates • positively regulates • negatively regulates • has_part is_a • If A is a B, then A is a subtype of B • mitotic cell cycle is a cell cycle • lyase activity is a catalytic activity. • Transitive relationship: can infer up the graph part_of • Necessarily part of • Wherever B exists, it is as part of A. But not all B is part of A. A • Transitive relationship (can infer up the graph) B regulates • One process directly affects another process or quality • Necessarily regulates: if both A and B are present, B always regulates A, but A may not always be regulated by B A B has_part • Relationships are upside down compared to is_a and part_of • Necessarily has part GO and GO Annotation, EBI Bioinformatics Roadshow. Düsseldorf. March 2011 is_a complete • For all terms in the ontology, you have to be able to reach the root through a complete path of is_a relationships: • we call this being is_a complete • important for reasoning over the ontology, and ontology development True path rule • Child terms inherit the meaning of all their parent terms. How is GO maintained? • GO editors and annotators work with experts to remodel specific areas of the ontology • Signaling • Kidney development • Transcription • Pathogenesis • Cell cycle • Deal with requests from the community • database curators, researchers, software developers • Some simple requests can be dealt with automatically • GO Consortium meetings for large changes • Mailing lists, conference calls, content workshops Requesting changes to the ontology • Public Source Forge (SF) tracker for term related issues https://sourceforge.net/projects/geneontology/ Why modify the GO? • GO reflects current knowledge of biology • Information from new organisms can make existing terms and arrangements incorrect • Not everything perfect from the outset • Improving definitions • Adding in synonyms and extra relationships Searching for GO terms http://www.ebi.ac.uk/QuickGO/ http://amigo.geneontology.org … there are more browsers available on the GO Tools page: http://www.geneontology.org/GO.tools.browsers.shtml The latest OBO Gene Ontology file can be downloaded from: http://www.geneontology.org/ontology/gene_ontology.obo Exercise Browsing the Gene Ontology using QuickGO • Exercise 1 15 mins PART II: GO Annotation A GO annotation is… A statement that a gene product: 1. has a particular molecular function Or is involved in a particular biological process Or is located within a certain cellular component 2. as determined by a particular evidence 3. as described in a particular reference Accession Name GO ID GO term name Reference Evidence Code P00505 GOT2 GO:0004069 Aspartate transaminase activity PMID:2731362 IDA Evidence codes http://www.geneontology.org/GO.evidence.shtml IDA: enzyme assay IPI: e.g. Y2H BLASTs, orthology comparison, HMMs subcategories of ISS review papers GO evidence code decision tree GOA makes annotations using two methods • Electronic • Quick way of producing large numbers of annotations • Annotations are less detailed • Manual • Time-consuming process producing lower numbers of annotations • Annotations are very detailed and accurate Electronic annotation by GOA • 1. Mapping of external concepts to GO terms • InterPro2GO (protein domains) • SPKW2GO (UniProt/Swiss-Prot keywords) • HAMAP2GO (Microbial protein annotation) • EC2GO (Enzyme Commission numbers) • SPSL2GO (Swiss-Prot subcellular locations) Electronic annotation by GOA Aspartate transaminase activity ; GO:0004069 lipid transport; GO:0006869 Electronic annotation by GOA • 2. Automatic transfer of annotations to orthologs Manual annotation by GOA • High-quality, specific annotations using: • Peer-reviewed papers • A range of evidence codes to categorize the types of evidence found in a paper www.ebi.ac.uk/GOA Finding annotations in a paper …for B. napus PERK1 protein (Q9ARH1) In this study, we report the isolation and molecular characterization of the B. napus PERK1 cDNA, that is predicted to encode a novel receptor-like kinase. We have shown that like other plant RLKs, the kinase domain of serine/threonine kinase , In addition, the PERK1 has serine/threonine kinaseactivity activity, location of a PERK1-GTP fusion protein to the plasma membrane supports the prediction that PERK1 is an integral membrane integral membraneprotein protein…these kinases have been implicated in early stages of wound woundresponse… response PubMed ID: 12374299 Function: protein serine/threonine kinase activity GO:0004674 Component: integral to plasma membrane GO:0005887 Process: response to wounding GO:0009611 Additional information • Qualifiers Modify the interpretation of an annotation • • • NOT (protein is not associated with the GO term) colocalizes_with (protein associates with complex but is not a bona fide member) contributes_to (describes action of a complex of proteins) • 'With' column Can include further information on the method being referenced e.g. the protein accession of an interacting protein The NOT qualifier • NOT is used to make an explicit note that the gene product is not associated with the GO term • Also used to document conflicting claims in the literature • NOT can be used with ALL three gene ontologies In these cells, SIPP1 was mainly present in the nucleus, where it displayed a non-uniform, speckled distribution and appeared to be excludedfrom from the nucleoli excluded the nucleoli. The colocalizes_with qualifier Gene products that are transiently associated with an organelle or complex ONLY used with GO component ontology The colocalizes_with qualifier Example (from Schizosaccharomyces pombe): Clp1 (Q9P7H1) relocalizes from the nucleolus to the spindle and site of cell division; i.e. it is associated transiently with the contractile ring (evidence from GFP fusion). The contributes_to qualifier • Where an individual gene product that is part of a complex can be annotated to terms that describe the action (function or process) of the whole complex • contributes_to is not needed to annotate a catalytic subunit. ONLY used with GO function ontology whether the the protein .. To test whether proteincomplex complex consisting of PIG-A, has GlcNAc transferase transferase activity PIG-H, PIG-C and hGPI1 has GlcNAc activity in vitro…. …incubation of the radiolabeled donor of GlcNAc, UDP[6-3H]GlcNAc, with lysates of JY5 cells transfected with resultedininsynthesis synthesis of GlcNAc-PI GST-tagged PIG-A resulted GlcNAc-PIand and itssubsequent subsequent deacetylation to glucosa- minyl Its deacetylation to glucosa-minyl phosphatidylinositol (GlcN-PI) phosphatidylinositol (GlcN-PI) WITH column • The with column provides supporting evidence for ISS, IPI, IGI and IC evidence codes ISS: the accession of the aligned protein/ortholog IPI: the accession of the interacting protein IGI: the accession of the interacting gene IC: The GO:ID for the inferred_from term WITH column How to access GO annotation data Where can you find annotations? UniProtKB Ensembl Entrez gene Gene Association Downloads • 17 column files containing all information for each annotation GO Consortium website GOA website GO browsers GO Slims GO slims • Many GO analysis tools use GO slims to give a broad overview of the dataset • GO slims are cut-down versions of the GO and contain a subset of the terms in the whole GO • GO slims usually contain less-specialised GO terms Slimming the GO using the ‘true path rule’ Many gene products are associated with a large number of descriptive, leaf GO nodes: Slimming the GO using the ‘true path rule’ …however annotations can be mapped up to a smaller set of parent GO terms: GO slims • Custom slims are available for download; http://www.geneontology.org/GO.slims.shtml • Or you can make your own using; • QuickGO • http://www.ebi.ac.uk/QuickGO • AmiGO's GO slimmer • http://amigo.geneontology.org/cgi-bin/amigo/slimmer Just some things to be aware of…. • The GO is continually changing • New terms created ontology • Existing terms obsoleted • Re-structured annotation • New annotations being created • ALWAYS use a current version of ontology and annotations • If publishing your analyses, please report the versions/dates you use: http://www.geneontology.org/GO.cite.shtml • Differences in representation of GO terms may be due to biological phenomenon. But also may be due to annotation-bias or experimental assays • Often better to remove the ‘NOT’ annotations before doing any large-scale analysis, as they can skew the results How scientists use the GO, and the tools they use for analysis Source of annotation • If you wanted to find out the role of a gene product manually, you’d have to read an awful lot of papers • But by using GO annotations, this work has already been done for you! GO:0006915 : apoptosis How scientists use the GO • Find out what a gene product does or which genes are involved in a certain biological process/function • Analyse high-throughput genomic or proteomic datasets • Validation of experimental techniques • Get a broad overview of a proteome • Obtain functional information for novel gene products Some examples… time Defense response Immune response Response to stimulus Toll regulated genes JAK-STAT regulated genes Puparial adhesion Molting cycle Hemocyanin MicroArray data analysis Amino acid catabolism Lipid metobolism Peptidase activity Protein catabolism Immune response Immune response Toll regulated genes attacked control ... lw n3d ...Colored on lw n3d pears ected Gene Tree: pearson Coloredby: by: t: Lis Gene Set_LW_n3d_5p_... n: nch color classification: Set_LW_n3d_5p_... Gene List: C5_RMA (Defa... of ofofCopy Copy Copy of Copy C5_RMA (Defa... genes allall genes (14010)(14010) Bregje Wertheim at the Centre for Evolutionary Genomics, Department of Biology, UCL and Eugene Schuster Group, EB Validation of experimental techniques Rat liver plasma membrane isolation (Cao et al., Journal of Proteome Research 2006) Analysis of high-throughput proteomic datasets Characterisation of proteins interacting with ribosomal protein S19 (Orrù et al., Molecular and Cellular Proteomics 2007) Obtain functional information for novel gene products MPYVSQSQHIDRVRGAIEGRLPAPGNSSRLVSSWQRSYEQYRLDPGSVIGPRVLTS SELR DVQGKEEAFLRASGQCLARLHDMIRMADYCVMLTDAHGVTIDYRIDRDRRGD FKHAGLYI GSCWSEREEGTCGIASVLTDLAPITVHKTDHFRAAFTTLTCSASPIFAPTG ELIGVLDAS AVQSPDNRDSQRLVFQLVRQSAALIEDGYFLNQTAQHWMIFGHASRN FVEAQPEVLIAFD ECGNIAASNRKAQECIAGLNGPRHVDEIFDTSAVHLHDVARTDTI MPLRLRATGAVLYAR IRAPLKRVSRSACAVSPSHSGQGTHDAHNDTNLDAISRFLHS RDSRIARNAEVALRIAGK HLPILILGETGVGKEVFAQALHASGARRAKPFVAVNCGAIP DSLIESELFGYAPGAFTGA RSRGARGKIAQAHGGTLFLDEIGDMPLNLQTRLLRVLA EGEVLPLGGDAPVRVDIDVICA THRDLARMVEEGTFREDLYYRLSGATLHMPPLRER ADILDVVHAVFDEEAQSAGHVLTLD GRLAERLARFSWPGNIRQLRNVLRYACAVCDS TRVELRHVSPDVAALLAPDEAALRPALA LENDERARIVDALTRHHWRPNAAAEALGM InterProScan Annotating novel sequences • Can use BLAST queries to find similar sequences with GO annotation which can be transferred to the new sequence • Two tools currently available; • AmiGO BLAST (from GO Consortium) http://amigo.geneontology.org/cgi-bin/amigo/blast.cgi • searches the GO Consortium database • BLAST2GO (from Babelomics) http://www.blast2go.org/ • searches the NCBI database AmiGO BLAST Exportin-T from Pongo abelii (Sumatran orangutan) Numerous Third Party Tools • Many tools exist that use GO to find common biological functions from a list of genes: http://www.geneontology.org/GO.tools.microarray.shtml GO tools: enrichment analysis • Most of these tools work in a similar way: • input a gene list and a subset of ‘interesting’ genes • tool shows which GO categories have most interesting genes associated with them i.e. which categories are ‘enriched’ for interesting genes • tool provides a statistical measure to determine whether enrichment is significant Exercises Searching for GO annotations in QuickGO • Exercise 2: using GO terms • Exercise 3: using a protein ID Using QuickGO to create a tailored set of annotations • Exercise 4: Filtering • Exercise 5: Statistics Map-up annotation using a GO slim • Exercise 6 Thanks for listening EBI is an Outstation of the European Molecular Biology Laboratory.