Multi-Species Network Inference Improves Gene Regulatory Network Reconstruction for Early Embryonic Development in Drosophila

被引:9
作者
Joshi, Anagha [1 ]
Beck, Yvonne [2 ]
Michoel, Tom [2 ]
机构
[1] Univ Edinburgh, Div Dev Biol, Roslin Inst, Edinburgh EH8 9YL, Midlothian, Scotland
[2] Univ Edinburgh, Div Genet & Genom, Roslin Inst, Edinburgh EH8 9YL, Midlothian, Scotland
基金
英国生物技术与生命科学研究理事会;
关键词
functional genomics; genomics; graphs and networks; gene networks; FUNCTIONAL ELEMENTS; EXPRESSION; EVOLUTION; DISCOVERY; MELANOGASTER; DIVERGENCE; CHALLENGES; BINDING;
D O I
10.1089/cmb.2014.0290
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Gene regulatory network inference uses genome-wide transcriptome measurements in response to genetic, environmental, or dynamic perturbations to predict causal regulatory influences between genes. We hypothesized that evolution also acts as a suitable network perturbation and that integration of data from multiple closely related species can lead to improved reconstruction of gene regulatory networks. To test this hypothesis, we predicted networks from temporal gene expression data for 3,610 genes measured during early embryonic development in six Drosophila species and compared predicted networks to gold standard networks of ChIP-chip and ChIP-seq interactions for developmental transcription factors in five species. We found that (i) the performance of single-species networks was independent of the species where the gold standard was measured; (ii) differences between predicted networks reflected the known phylogeny and differences in biology between the species; (iii) an integrative consensus network that minimized the total number of edge gains and losses with respect to all single-species networks performed better than any individual network. Our results show that in an evolutionarily conserved system, integration of data from comparable experiments in multiple species improves the inference of gene regulatory networks. They provide a basis for future studies on the numerous multispecies gene expression datasets for other biological processes available in the literature.
引用
收藏
页码:253 / 265
页数:13
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