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Modeling the Drosophila Gene Cluster Regulation Network for Muscle Development

The development of accurate and reliable dynamical modeling procedures that describe the time evolution of gene expression levels is a prerequisite to understanding and controlling the transcription process. We focused on data from DNA microarray time series for 20 Drosophila genes involved in muscl...

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Detalles Bibliográficos
Autores principales: Haye, Alexandre, Albert, Jaroslav, Rooman, Marianne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3940846/
https://www.ncbi.nlm.nih.gov/pubmed/24594656
http://dx.doi.org/10.1371/journal.pone.0090285
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author Haye, Alexandre
Albert, Jaroslav
Rooman, Marianne
author_facet Haye, Alexandre
Albert, Jaroslav
Rooman, Marianne
author_sort Haye, Alexandre
collection PubMed
description The development of accurate and reliable dynamical modeling procedures that describe the time evolution of gene expression levels is a prerequisite to understanding and controlling the transcription process. We focused on data from DNA microarray time series for 20 Drosophila genes involved in muscle development during the embryonic stage. Genes with similar expression profiles were clustered on the basis of a translation-invariant and scale-invariant distance measure. The time evolution of these clusters was modeled using coupled differential equations. Three model structures involving a transcription term and a degradation term were tested. The parameters were identified in successive steps: network construction, parameter optimization, and parameter reduction. The solutions were evaluated on the basis of the data reproduction and the number of parameters, as well as on two biology-based requirements: the robustness with respect to parameter variations and the values of the expression levels not being unrealistically large upon extrapolation in time. Various solutions were obtained that satisfied all our evaluation criteria. The regulatory networks inferred from these solutions were compared with experimental data. The best solution has half of the experimental connections, which compares favorably with previous approaches. Biasing the network toward the experimental connections led to the identification of a model that is only slightly less good on the basis of the evaluation criteria. The non-uniqueness of the solutions and the variable agreement with experimental connections were discussed in the context of the different hypotheses underlying this type of approach.
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spelling pubmed-39408462014-03-06 Modeling the Drosophila Gene Cluster Regulation Network for Muscle Development Haye, Alexandre Albert, Jaroslav Rooman, Marianne PLoS One Research Article The development of accurate and reliable dynamical modeling procedures that describe the time evolution of gene expression levels is a prerequisite to understanding and controlling the transcription process. We focused on data from DNA microarray time series for 20 Drosophila genes involved in muscle development during the embryonic stage. Genes with similar expression profiles were clustered on the basis of a translation-invariant and scale-invariant distance measure. The time evolution of these clusters was modeled using coupled differential equations. Three model structures involving a transcription term and a degradation term were tested. The parameters were identified in successive steps: network construction, parameter optimization, and parameter reduction. The solutions were evaluated on the basis of the data reproduction and the number of parameters, as well as on two biology-based requirements: the robustness with respect to parameter variations and the values of the expression levels not being unrealistically large upon extrapolation in time. Various solutions were obtained that satisfied all our evaluation criteria. The regulatory networks inferred from these solutions were compared with experimental data. The best solution has half of the experimental connections, which compares favorably with previous approaches. Biasing the network toward the experimental connections led to the identification of a model that is only slightly less good on the basis of the evaluation criteria. The non-uniqueness of the solutions and the variable agreement with experimental connections were discussed in the context of the different hypotheses underlying this type of approach. Public Library of Science 2014-03-03 /pmc/articles/PMC3940846/ /pubmed/24594656 http://dx.doi.org/10.1371/journal.pone.0090285 Text en © 2014 Haye et al http://creativecommons.org/licenses/by/4.0/ 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 properly credited.
spellingShingle Research Article
Haye, Alexandre
Albert, Jaroslav
Rooman, Marianne
Modeling the Drosophila Gene Cluster Regulation Network for Muscle Development
title Modeling the Drosophila Gene Cluster Regulation Network for Muscle Development
title_full Modeling the Drosophila Gene Cluster Regulation Network for Muscle Development
title_fullStr Modeling the Drosophila Gene Cluster Regulation Network for Muscle Development
title_full_unstemmed Modeling the Drosophila Gene Cluster Regulation Network for Muscle Development
title_short Modeling the Drosophila Gene Cluster Regulation Network for Muscle Development
title_sort modeling the drosophila gene cluster regulation network for muscle development
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3940846/
https://www.ncbi.nlm.nih.gov/pubmed/24594656
http://dx.doi.org/10.1371/journal.pone.0090285
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