A Coordinated Approach by Public Domain Bioinformatics Resources to Aid the Fight Against Alzheimer’s Disease Through Expert Curation of Key Protein Targets

Author:

Breuza Lionel1,Arighi Cecilia N.23,Argoud-Puy Ghislaine1,Casals-Casas Cristina1,Estreicher Anne1,Famiglietti Maria Livia1,Georghiou George4,Gos Arnaud1,Gruaz-Gumowski Nadine1,Hinz Ursula1,Hyka-Nouspikel Nevila1,Kramarz Barbara5,Lovering Ruth C.5,Lussi Yvonne4,Magrane Michele4,Masson Patrick1,Perfetto Livia4,Poux Sylvain1,Rodriguez-Lopez Milagros4,Stoeckert Christian6,Sundaram Shyamala1,Wang Li-San6,Wu Elizabeth7,Orchard Sandra4ORCID,

Affiliation:

1. Swiss-Prot Group, SIB Swiss Institute of Bioinformatics, Centre Medical Universitaire, Geneva, Switzerland

2. Protein Information Resource, Georgetown University Medical Center, Washington, DC, USA

3. Protein Information Resource, University of Delaware, Newark, DE, USA

4. European Molecular Biology Laboratory, European Bioinformatics Institute (EMBL-EBI), Wellcome Trust Campus, Hinxton, Cambridge, UK

5. Functional Gene Annotation, Preclinical and Fundamental Science, Institute of Cardiovascular Science, University College London (UCL), London, UK

6. Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA

7. Alzforum, Cambridge, MA, USA

Abstract

Background: The analysis and interpretation of data generated from patient-derived clinical samples relies on access to high-quality bioinformatics resources. These are maintained and updated by expert curators extracting knowledge from unstructured biological data described in free-text journal articles and converting this into more structured, computationally-accessible forms. This enables analyses such as functional enrichment of sets of genes/proteins using the Gene Ontology, and makes the searching of data more productive by managing issues such as gene/protein name synonyms, identifier mapping, and data quality. Objective: To undertake a coordinated annotation update of key public-domain resources to better support Alzheimer’s disease research. Methods: We have systematically identified target proteins critical to disease process, in part by accessing informed input from the clinical research community. Results: Data from 954 papers have been added to the UniProtKB, Gene Ontology, and the International Molecular Exchange Consortium (IMEx) databases, with 299 human proteins and 279 orthologs updated in UniProtKB. 745 binary interactions were added to the IMEx human molecular interaction dataset. Conclusion: This represents a significant enhancement in the expert curated data pertinent to Alzheimer’s disease available in a number of biomedical databases. Relevant protein entries have been updated in UniProtKB and concomitantly in the Gene Ontology. Molecular interaction networks have been significantly extended in the IMEx Consortium dataset and a set of reference protein complexes created. All the resources described are open-source and freely available to the research community and we provide examples of how these data could be exploited by researchers.

Publisher

IOS Press

Subject

Psychiatry and Mental health,Geriatrics and Gerontology,Clinical Psychology,General Medicine,General Neuroscience

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