Heydari, Tiam and Langley, Matthew A. and Fisher, Cynthia L. and Aguilar-Hidalgo, Daniel and Shukla, Shreya and Yachie-Kinoshita, Ayako and Hughes, Michael and McNagny, Kelly M. and Zandstra, Peter W. (2022) IQCELL: A platform for predicting the effect of gene perturbations on developmental trajectories using single-cell RNA-seq data. PLoS Computational Biology, 18 (2). Art. No. e1009907. ISSN 1553-734X. PMCID PMC8906617. doi:10.1101/2021.04.01.438014. https://resolver.caltech.edu/CaltechAUTHORS:20210405-071808216
Use this Persistent URL to link to this item: https://resolver.caltech.edu/CaltechAUTHORS:20210405-071808216
Abstract
The increasing availability of single-cell RNA-sequencing (scRNA-seq) data from various developmental systems provides the opportunity to infer gene regulatory networks (GRNs) directly from data. Herein we describe IQCELL, a platform to infer, simulate, and study executable logical GRNs directly from scRNA-seq data. Such executable GRNs allow simulation of fundamental hypotheses governing developmental programs and help accelerate the design of strategies to control stem cell fate. We first describe the architecture of IQCELL. Next, we apply IQCELL to scRNA-seq datasets from early mouse T-cell and red blood cell development, and show that the platform can infer overall over 74% of causal gene interactions previously reported from decades of research. We will also show that dynamic simulations of the generated GRN qualitatively recapitulate the effects of known gene perturbations. Finally, we implement an IQCELL gene selection pipeline that allows us to identify candidate genes, without prior knowledge. We demonstrate that GRN simulations based on the inferred set yield results similar to the original curated lists. In summary, the IQCELL platform offers a versatile tool to infer, simulate, and study executable GRNs in dynamic biological systems.
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Additional Information: | © 2022 Heydari et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Received: August 20, 2021; Accepted: February 8, 2022; Published: February 25, 2022. We thank Sara-Jane Dunn, Boyan Yordanov, and Ellen V. Rothenberg for our fruitful discussions and Yale S. Michaels and John M. Edgar for critically reading the manuscript. We also thank Microsoft Research (Cambridge, UK) and Sara-Jane Dunn for facilitating the opportunity for the author to deepen his understanding of the Z3 reasoning engine. We thank Ellen V. Rothenberg, and Bertie Gottgens for generating publicly available high-quality scRNA-seq data sets that have been used in this study. TH, MAL, AYK, CLF, DAH, SS, and PWZ were supported by the Canadian Institutes of Health Research (CIHR), Foundation Grant FRN 154283, and the Natural Sciences and Engineering Research Council of Canada (NSERC), Discovery Grant RGPIN-2020-06496), to PWZ. PWZ is the Canada Research Chair in Stem Cell Bioengineering (https://www.chairs-chaires.gc.ca). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. Peer Review History: PLOS recognizes the benefits of transparency in the peer review process; therefore, we enable the publication of all of the content of peer review and author responses alongside final, published articles. The editorial history of this article is available here: https://doi.org/10.1371/journal.pcbi.1009907. Author Contributions: Conceptualization: Tiam Heydari, Peter W. Zandstra. Investigation: Matthew A. Langley, Cynthia L. Fisher, Shreya Shukla, Michael Hughes. Methodology: Tiam Heydari. Resources: Kelly M. McNagny. Software: Tiam Heydari, Matthew A. Langley, Ayako Yachie-Kinoshita. Supervision: Peter W. Zandstra. Writing – original draft: Tiam Heydari, Daniel Aguilar-Hidalgo, Peter W. Zandstra. Writing – review & editing: Tiam Heydari, Matthew A. Langley, Cynthia L. Fisher, Daniel Aguilar-Hidalgo, Kelly M. McNagny, Peter W. Zandstra. The authors have declared that no competing interests exist. Data Availability Statement: The source code of IQCELL python package generated during this study and example notebooks of IQCELL’s implementation are available on Gitlab: (https://gitlab.com/stemcellbioengineering/iqcell). The raw sequencing data generated in this study have been submitted to GEO under the accession number GSE196972. | ||||||||||||||||||||
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Issue or Number: | 2 | ||||||||||||||||||||
PubMed Central ID: | PMC8906617 | ||||||||||||||||||||
DOI: | 10.1101/2021.04.01.438014 | ||||||||||||||||||||
Record Number: | CaltechAUTHORS:20210405-071808216 | ||||||||||||||||||||
Persistent URL: | https://resolver.caltech.edu/CaltechAUTHORS:20210405-071808216 | ||||||||||||||||||||
Official Citation: | Heydari T, A. Langley M, Fisher CL, Aguilar-Hidalgo D, Shukla S, Yachie-Kinoshita A, et al. (2022) IQCELL: A platform for predicting the effect of gene perturbations on developmental trajectories using single-cell RNA-seq data. PLoS Comput Biol 18(2): e1009907. https://doi.org/10.1371/journal.pcbi.1009907 | ||||||||||||||||||||
Usage Policy: | No commercial reproduction, distribution, display or performance rights in this work are provided. | ||||||||||||||||||||
ID Code: | 108616 | ||||||||||||||||||||
Collection: | CaltechAUTHORS | ||||||||||||||||||||
Deposited By: | Tony Diaz | ||||||||||||||||||||
Deposited On: | 08 Apr 2021 20:50 | ||||||||||||||||||||
Last Modified: | 25 Mar 2022 20:23 |
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