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Automatic mechanistic inference from large families of Boolean models generated by Monte Carlo tree search

Many important processes in biology, such as signaling and gene regulation, can be described using logic models. These logic models are typically built to behaviorally emulate experimentally observed phenotypes, which are assumed to be steady states of a biological system. Most models are built by h...

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Detalles Bibliográficos
Autores principales: Glazer, Bryan J., Lifferth, Jonathan T., Lopez, Carlos F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10485623/
https://www.ncbi.nlm.nih.gov/pubmed/37691824
http://dx.doi.org/10.3389/fcell.2023.1198359
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author Glazer, Bryan J.
Lifferth, Jonathan T.
Lopez, Carlos F.
author_facet Glazer, Bryan J.
Lifferth, Jonathan T.
Lopez, Carlos F.
author_sort Glazer, Bryan J.
collection PubMed
description Many important processes in biology, such as signaling and gene regulation, can be described using logic models. These logic models are typically built to behaviorally emulate experimentally observed phenotypes, which are assumed to be steady states of a biological system. Most models are built by hand and therefore researchers are only able to consider one or perhaps a few potential mechanisms. We present a method to automatically synthesize Boolean logic models with a specified set of steady states. Our method, called MC-Boomer, is based on Monte Carlo Tree Search an efficient, parallel search method using reinforcement learning. Our approach enables users to constrain the model search space using prior knowledge or biochemical interaction databases, thus leading to generation of biologically plausible mechanistic hypotheses. Our approach can generate very large numbers of data-consistent models. To help develop mechanistic insight from these models, we developed analytical tools for multi-model inference and model selection. These tools reveal the key sets of interactions that govern the behavior of the models. We demonstrate that MC-Boomer works well at reconstructing randomly generated models. Then, using single time point measurements and reasonable biological constraints, our method generates hundreds of thousands of candidate models that match experimentally validated in-vivo behaviors of the Drosophila segment polarity network. Finally we outline how our multi-model analysis procedures elucidate potentially novel biological mechanisms and provide opportunities for model-driven experimental validation.
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spelling pubmed-104856232023-09-09 Automatic mechanistic inference from large families of Boolean models generated by Monte Carlo tree search Glazer, Bryan J. Lifferth, Jonathan T. Lopez, Carlos F. Front Cell Dev Biol Cell and Developmental Biology Many important processes in biology, such as signaling and gene regulation, can be described using logic models. These logic models are typically built to behaviorally emulate experimentally observed phenotypes, which are assumed to be steady states of a biological system. Most models are built by hand and therefore researchers are only able to consider one or perhaps a few potential mechanisms. We present a method to automatically synthesize Boolean logic models with a specified set of steady states. Our method, called MC-Boomer, is based on Monte Carlo Tree Search an efficient, parallel search method using reinforcement learning. Our approach enables users to constrain the model search space using prior knowledge or biochemical interaction databases, thus leading to generation of biologically plausible mechanistic hypotheses. Our approach can generate very large numbers of data-consistent models. To help develop mechanistic insight from these models, we developed analytical tools for multi-model inference and model selection. These tools reveal the key sets of interactions that govern the behavior of the models. We demonstrate that MC-Boomer works well at reconstructing randomly generated models. Then, using single time point measurements and reasonable biological constraints, our method generates hundreds of thousands of candidate models that match experimentally validated in-vivo behaviors of the Drosophila segment polarity network. Finally we outline how our multi-model analysis procedures elucidate potentially novel biological mechanisms and provide opportunities for model-driven experimental validation. Frontiers Media S.A. 2023-08-25 /pmc/articles/PMC10485623/ /pubmed/37691824 http://dx.doi.org/10.3389/fcell.2023.1198359 Text en Copyright © 2023 Glazer, Lifferth and Lopez. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cell and Developmental Biology
Glazer, Bryan J.
Lifferth, Jonathan T.
Lopez, Carlos F.
Automatic mechanistic inference from large families of Boolean models generated by Monte Carlo tree search
title Automatic mechanistic inference from large families of Boolean models generated by Monte Carlo tree search
title_full Automatic mechanistic inference from large families of Boolean models generated by Monte Carlo tree search
title_fullStr Automatic mechanistic inference from large families of Boolean models generated by Monte Carlo tree search
title_full_unstemmed Automatic mechanistic inference from large families of Boolean models generated by Monte Carlo tree search
title_short Automatic mechanistic inference from large families of Boolean models generated by Monte Carlo tree search
title_sort automatic mechanistic inference from large families of boolean models generated by monte carlo tree search
topic Cell and Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10485623/
https://www.ncbi.nlm.nih.gov/pubmed/37691824
http://dx.doi.org/10.3389/fcell.2023.1198359
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