Consistent prediction of GO protein localization

• Published in: Scientific reports 2018-05, Vol.8 (1), p.7757-12, Article 7757
• Main Authors: Spetale, Flavio E., Arce, Debora, Krsticevic, Flavia, Bulacio, Pilar, Tapia, Elizabeth
• Format: Article
• Language: English
• Subjects: 631/114; 631/114/2397; Annotations; Gene duplication; Humanities and Social Sciences; Learning algorithms; Localization; Macromolecules; multidisciplinary; Ontology; Proteins; Science; Science (multidisciplinary); Tomatoes
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-018-26041-z

The GO-Cellular Component (GO-CC) ontology provides a controlled vocabulary for the consistent description of the subcellular compartments or macromolecular complexes where proteins may act. Current machine learning-based methods used for the automated GO-CC annotation of proteins suffer from the inconsistency of individual GO-CC term predictions. Here, we present FGGA-CC + , a class of hierarchical graph-based classifiers for the consistent GO-CC annotation of protein coding genes at the subcellular compartment or macromolecular complex levels. Aiming to boost the accuracy of GO-CC predictions, we make use of the protein localization knowledge in the GO-Biological Process (GO-BP) annotations to boost the accuracy of GO-CC prediction. As a result, FGGA-CC + classifiers are built from annotation data in both the GO-CC and GO-BP ontologies. Due to their graph-based design, FGGA-CC + classifiers are fully interpretable and their predictions amenable to expert analysis. Promising results on protein annotation data from five model organisms were obtained. Additionally, successful validation results in the annotation of a challenging subset of tandem duplicated genes in the tomato non-model organism were accomplished. Overall, these results suggest that FGGA-CC + classifiers can indeed be useful for satisfying the huge demand of GO-CC annotation arising from ubiquitous high throughout sequencing and proteomic projects.