4.7 Article Proceedings Paper

Integration of molecular network data reconstructs Gene Ontology

Journal

BIOINFORMATICS
Volume 30, Issue 17, Pages I594-I600

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/bioinformatics/btu470

Keywords

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Funding

  1. European Research Council (ERC) [278212]
  2. National Science Foundation (NSF) Cyber-Enabled Discovery and Innovation (CDI) [OIA-1028394]
  3. Serbian Ministry of Education and Science [III44006]
  4. ARRS [J1-5454]
  5. Office Of The Director
  6. Office of Integrative Activities [1028394] Funding Source: National Science Foundation

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Motivation: Recently, a shift was made from using Gene Ontology (GO) to evaluate molecular network data to using these data to construct and evaluate GO. Dutkowski et al. provide the first evidence that a large part of GO can be reconstructed solely from topologies of molecular networks. Motivated by this work, we develop a novel data integration framework that integrates multiple types of molecular network data to reconstruct and update GO. We ask how much of GO can be recovered by integrating various molecular interaction data. Results: We introduce a computational framework for integration of various biological networks using penalized non-negative matrix tri-factorization (PNMTF). It takes all network data in a matrix form and performs simultaneous clustering of genes and GO terms, inducing new relations between genes and GO terms (annotations) and between GO terms themselves. To improve the accuracy of our predicted relations, we extend the integration methodology to include additional topological information represented as the similarity in wiring around non-interacting genes. Surprisingly, by integrating topologies of bakers' yeasts protein-protein interaction, genetic interaction (GI) and co-expression networks, our method reports as related 96% of GO terms that are directly related in GO. The inclusion of the wiring similarity of non-interacting genes contributes 6% to this large GO term association capture. Furthermore, we use our method to infer new relationships between GO terms solely from the topologies of these networks and validate 44% of our predictions in the literature. In addition, our integration method reproduces 48% of cellular component, 41% of molecular function and 41% of biological process GO terms, outperforming the previous method in the former two domains of GO. Finally, we predict new GO annotations of yeast genes and validate our predictions through GIs profiling.

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