Dynamic regulatory module networks for inference of cell type–specific transcriptional networks

  1. Sushmita Roy1,2,7
  1. 1Wisconsin Institute for Discovery, University of Wisconsin, Madison, Wisconsin 53715, USA;
  2. 2Department of Computer Sciences, University of Wisconsin, Madison, Wisconsin 53715, USA;
  3. 3Morgridge Institute for Research, Madison, Wisconsin 53715, USA;
  4. 4Molecular and Environmental Toxicology Program, University of Wisconsin, Madison, Wisconsin 53715, USA;
  5. 5Department of Cell and Regenerative Biology, University of Wisconsin, Madison, Wisconsin 53715, USA;
  6. 6Department of Molecular, Cellular, and Developmental Biology, University of California, Santa Barbara, California 93117, USA;
  7. 7Department of Biostatistics and Medical Informatics, University of Wisconsin, Madison, Wisconsin 53715, USA
  1. 8 These authors contributed equally to this work.

  • 9 Present address: Division of Reproductive Sciences, Department of Obstetrics and Gynecology, University of Wisconsin, Madison, WI 53715, USA

  • Corresponding author: sroy{at}biostat.wisc.edu
  • Abstract

    Changes in transcriptional regulatory networks can significantly alter cell fate. To gain insight into transcriptional dynamics, several studies have profiled bulk multi-omic data sets with parallel transcriptomic and epigenomic measurements at different stages of a developmental process. However, integrating these data to infer cell type–specific regulatory networks is a major challenge. We present dynamic regulatory module networks (DRMNs), a novel approach to infer cell type–specific cis-regulatory networks and their dynamics. DRMN integrates expression, chromatin state, and accessibility to predict cis-regulators of context-specific expression, where context can be cell type, developmental stage, or time point, and uses multitask learning to capture network dynamics across linearly and hierarchically related contexts. We applied DRMNs to study regulatory network dynamics in three developmental processes, each showing different temporal relationships and measuring a different combination of regulatory genomic data sets: cellular reprogramming, liver dedifferentiation, and forward differentiation. DRMN identified known and novel regulators driving cell type–specific expression patterns, showing its broad applicability to examine dynamics of gene regulatory networks from linearly and hierarchically related multi-omic data sets.

    Footnotes

    • [Supplemental material is available for this article.]

    • Article published online before print. Article, supplemental material, and publication date are at https://www.genome.org/cgi/doi/10.1101/gr.276542.121.

    • Freely available online through the Genome Research Open Access option.

    • Received December 28, 2021.
    • Accepted June 2, 2022.

    This article, published in Genome Research, is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/.

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