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

Author:

Pio Gianvito12ORCID,Mignone Paolo12ORCID,Magazzù Giuseppe3,Zampieri Guido34ORCID,Ceci Michelangelo125ORCID,Angione Claudio367ORCID

Affiliation:

1. Department of Computer Science, University of Bari Aldo Moro, Bari 70125, Italy

2. Big Data Lab, National Interuniversity Consortium for Informatics (CINI), Rome 00185, Italy

3. School of Computing, Engineering & Digital Technologies, Teesside University, Tees Valley TS1 3BA, UK

4. Department of Biology, University of Padova, Padova 35121, Italy

5. Department of Knowledge Technologies, Jozef Stefan Institute, Ljubljana 1000, Slovenia

6. Centre for Digital Innovation, Teesside University, Campus Heart, Tees Valley TS1 3BX, UK

7. Healthcare Innovation Centre, Teesside University, Campus Heart, Tees Valley TS1 3BX, UK

Abstract

Abstract 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. Availability and implementation The method, the datasets and all the results obtained in this study are available at: https://doi.org/10.6084/m9.figshare.c.5237687. Supplementary information Supplementary data are available at Bioinformatics online.

Funder

Ministry of Universities and Research

Big Data Analytics

UKRI Research England’s THYME

Children’s Liver Disease Foundation Research

Apulia Region through the ‘Research for Innovation—REFIN’

Publisher

Oxford University Press (OUP)

Subject

Computational Mathematics,Computational Theory and Mathematics,Computer Science Applications,Molecular Biology,Biochemistry,Statistics and Probability

Cited by 31 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3