Inter-species pathway perturbation prediction via data-driven detection of functional homology

Bioinformatics. 2015 Feb 15;31(4):501-8. doi: 10.1093/bioinformatics/btu570. Epub 2014 Aug 22.

Abstract

Motivation: Experiments in animal models are often conducted to infer how humans will respond to stimuli by assuming that the same biological pathways will be affected in both organisms. The limitations of this assumption were tested in the IMPROVER Species Translation Challenge, where 52 stimuli were applied to both human and rat cells and perturbed pathways were identified. In the Inter-species Pathway Perturbation Prediction sub-challenge, multiple teams proposed methods to use rat transcription data from 26 stimuli to predict human gene set and pathway activity under the same perturbations. Submissions were evaluated using three performance metrics on data from the remaining 26 stimuli.

Results: We present two approaches, ranked second in this challenge, that do not rely on sequence-based orthology between rat and human genes to translate pathway perturbation state but instead identify transcriptional response orthologs across a set of training conditions. The translation from rat to human accomplished by these so-called direct methods is not dependent on the particular analysis method used to identify perturbed gene sets. In contrast, machine learning-based methods require performing a pathway analysis initially and then mapping the pathway activity between organisms. Unlike most machine learning approaches, direct methods can be used to predict the activation of a human pathway for a new (test) stimuli, even when that pathway was never activated by a training stimuli.

Availability: Gene expression data are available from ArrayExpress (accession E-MTAB-2091), while software implementations are available from http://bioinformaticsprb.med.wayne.edu?p=50 and http://goo.gl/hJny3h.

Contact: [email protected] or [email protected].

Supplementary information: Supplementary data are available at Bioinformatics online.

Publication types

  • Comparative Study
  • Research Support, N.I.H., Extramural
  • Research Support, N.I.H., Intramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Algorithms*
  • Animals
  • Artificial Intelligence*
  • Bronchi / cytology
  • Bronchi / metabolism
  • Cells, Cultured
  • Cytokines / metabolism*
  • Databases, Factual
  • Epithelial Cells / cytology
  • Epithelial Cells / metabolism
  • Gene Expression Profiling / methods*
  • Gene Expression Regulation
  • Humans
  • Models, Animal
  • Oligonucleotide Array Sequence Analysis
  • Phosphoproteins / metabolism*
  • Phosphorylation
  • Rats
  • Signal Transduction
  • Software*
  • Species Specificity
  • Systems Biology / methods*
  • Translational Research, Biomedical

Substances

  • Cytokines
  • Phosphoproteins