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bioRxiv · 10.1101/2019.12.20.884163

Gene network reconstruction using single cell transcriptomic data reveals key factors for embryonic stem cell differentiation

Kim, J.·Jakobsen, S. T.·Natarajan, K. N.·Won, K. J.
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Abstract

Accurate prediction of gene regulatory rules is important towards understanding of cellular processes. Existing computational algorithms devised for bulk transcriptomics typically require a large number of time points to infer gene regulatory networks (GRNs), are applicable for a small number of genes, and fail to detect potential causal relationships effectively. Here, we propose a novel approach TENET to reconstruct GRNs from single cell RNA sequencing (scRNAseq) datasets. Employing transfer entropy (TE) to measure the amount of causal relationships between genes, TENET predicts large-scale gene regulatory cascades/relationships from scRNAseq data. TENET showed better performance than other GRN reconstructors, in identifying key regulators from public datasets. Specifically from scRNAseq, TENET identified key transcriptional factors in embryonic stem cells (ESCs) and during direct cardiomyocytes reprogramming, where other predictors failed. We further demonstrate that known target genes have significantly higher TE values, and TENET predicted higher TE genes were more influenced by the perturbation of their regulator. Using TENET, we identified and validated that Nme2 is a culture condition specific stem cell factor. These results indicate that TENET is uniquely capable of identifying key regulators from scRNAseq data. Key PointsO_LITENET measures putative causal relationships between genes using transfer entropy. C_LIO_LITENET shows outstanding performance in identifying key regulators compared to existing methods. C_LIO_LITENET can reveal previously uncharacterized regulators. C_LI

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Kim, J., Jakobsen, S. T., Natarajan, K. N., Won, K. J.. 2019-12-21. Gene network reconstruction using single cell transcriptomic data reveals key factors for embryonic stem cell differentiation. https://doi.org/10.1101/2019.12.20.884163

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