4.7 Article

Inference of gene regulatory networks from genome-wide knockout fitness data

期刊

BIOINFORMATICS
卷 29, 期 3, 页码 338-346

出版社

OXFORD UNIV PRESS
DOI: 10.1093/bioinformatics/bts634

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资金

  1. Office of Science, Office of Biological and Environmental Research, of the U. S. Department of Energy [DE-AC02-05CH11231]
  2. U.S. National Science Foundation (NSF) grant [DBI-0850030]
  3. Columbia Open-Access Publication (COAP) Fund
  4. Direct For Biological Sciences
  5. Div Of Biological Infrastructure [0850205] Funding Source: National Science Foundation
  6. Div Of Biological Infrastructure
  7. Direct For Biological Sciences [0850030] Funding Source: National Science Foundation

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Motivation: Genome-wide fitness is an emerging type of high-throughput biological data generated for individual organisms by creating libraries of knockouts, subjecting them to broad ranges of environmental conditions, and measuring the resulting clone-specific fitnesses. Since fitness is an organism-scale measure of gene regulatory network behaviour, it may offer certain advantages when insights into such phenotypical and functional features are of primary interest over individual gene expression. Previous works have shown that genome-wide fitness data can be used to uncover novel gene regulatory interactions, when compared with results of more conventional gene expression analysis. Yet, to date, few algorithms have been proposed for systematically using genome-wide mutant fitness data for gene regulatory network inference. Results: In this article, we describe a model and propose an inference algorithm for using fitness data from knockout libraries to identify underlying gene regulatory networks. Unlike most prior methods, the presented approach captures not only structural, but also dynamical and non-linear nature of biomolecular systems involved. A state-space model with non-linear basis is used for dynamically describing gene regulatory networks. Network structure is then elucidated by estimating unknown model parameters. Unscented Kalman filter is used to cope with the non-linearities introduced in the model, which also enables the algorithm to run in on-line mode for practical use. Here, we demonstrate that the algorithm provides satisfying results for both synthetic data as well as empirical measurements of GAL network in yeast Saccharomyces cerevisiae and TyrR-LiuR network in bacteria Shewanella oneidensis.

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