4.7 Article

Integrating genome-scale metabolic modelling and transfer learning for human gene regulatory network reconstruction

Journal

BIOINFORMATICS
Volume 38, Issue 2, Pages 487-493

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/bioinformatics/btab647

Keywords

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Funding

  1. Ministry of Universities and Research through the project 'Big Data Analytics' [AIM 1852414-1]
  2. UKRI Research England's THYME project
  3. Children's Liver Disease Foundation Research Grant
  4. Apulia Region through the 'Research for Innovation-REFIN' initiative [7EDD092A]

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Researchers proposed a novel method for reconstructing the human gene regulatory network based on a transfer learning strategy that combines information from human and mouse, utilizing gene-related metabolic features. Experimental results showed that this method provides a significant advantage in terms of reconstruction accuracy and additional clues about the contribution of each metabolic feature.
Motivation: Gene regulation is responsible for controlling numerous physiological functions and dynamically responding to environmental fluctuations. Reconstructing the human network of gene regulatory interactions is thus paramount to understanding the cell functional organization across cell types, as well as to elucidating pathogenic processes and identifying molecular drug targets. Although significant effort has been devoted towards this direction, existing computational methods mainly rely on gene expression levels, possibly ignoring the information conveyed by mechanistic biochemical knowledge. Moreover, except for a few recent attempts, most of the existing approaches only consider the information of the organism under analysis, without exploiting the information of related model organisms. Results: We propose a novel method for the reconstruction of the human gene regulatory network, based on a transfer learning strategy that synergically exploits information from human and mouse, conveyed by gene-related metabolic features generated in silico from gene expression data. Specifically, we learn a predictive model from metabolic activity inferred via tissue-specific metabolic modelling of artificial gene knockouts. Our experiments show that the combination of our transfer learning approach with the constructed metabolic features provides a significant advantage in terms of reconstruction accuracy, as well as additional clues on the contribution of each constructed metabolic feature.

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