Abstract

Gene regulatory network (GRN) inference can now take advantage of powerful machine learning algorithms to complement traditional experimental methods in building gene networks. However, the dynamical nature of embryonic development–representing the time-dependent interactions between thousands of transcription factors, signaling molecules, and effector genes–is one of the most challenging arenas for GRN prediction. In this work, we show that successful GRN predictions for a developmental network from gene expression data alone can be obtained with the Priors Enriched Absent Knowledge (PEAK) network inference algorithm. PEAK is a noise-robust method that models gene expression dynamics via ordinary differential equations and selects the best network based on information-theoretic criteria coupled with the machine learning algorithm Elastic Net. We test our GRN prediction methodology using two gene expression datasets for the purple sea urchin, Stronglyocentrotus purpuratus, and cross-check our results against existing GRN models that have been constructed and validated by over 30 years of experimental results. Our results find a remarkably high degree of sensitivity in identifying known gene interactions in the network (maximum 81.58%). We also generate novel predictions for interactions that have not yet been described, which provide a resource for researchers to use to further complete the sea urchin GRN. Published ChIPseq data and spatial co-expression analysis further support a subset of the top novel predictions. We conclude that GRN predictions that match known gene interactions can be produced using gene expression data alone from developmental time series experiments.

Highlights

  • Transcription factors regulate cell-specific gene expression to create phenotypes, respond to disease, drive evolution, and guide embryonic development [1]

  • Gene regulatory network (GRN) models are concerned with genes whose expression is regulated and the regulators themselves

  • To identify the set of regulated genes to input into the Priors Enriched Absent Knowledge (PEAK) machine learning algorithm, we started with the sea urchin RNAseq transcriptome dataset covering 0-72hpf, which represents genes expressed during embryogenesis [18]

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Summary

Introduction

Transcription factors regulate cell-specific gene expression to create phenotypes, respond to disease, drive evolution, and guide embryonic development [1]. Developmental gene regulatory network inference by machine learning. GRN models are routinely used to follow the causal links from regulatory genes to cell fate decisions or cell activities. Using a GRN model to create hypotheses about the function of actors in a regulatory program aids in experimental design. Animal and plant developmental programs have been described by GRN models, beginning with the construction of the sea urchin endomesoderm GRN [3, 4] and followed soon thereafter by the Drosophila melanogaster dorsoventral patterning network [5, 6] and the Xenopus laevis mesoderm specification network [7]. There is a pressing need to facilitate GRN modeling using computational prediction tools to help fill in the gaps in existing GRNs and to help create new GRN models with testable predictions

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