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Improving Gene Regulatory Network Inference by Incorporating Rates of Transcriptional Changes

Organisms respond to changes in their environment through transcriptional regulatory networks (TRNs). The regulatory hierarchy of these networks can be inferred from expression data. Computational approaches to identify TRNs can be applied in any species where quality RNA can be acquired, However, C...

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Autores principales: Desai, Jigar S., Sartor, Ryan C., Lawas, Lovely Mae, Jagadish, S. V. Krishna, Doherty, Colleen J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5722905/
https://www.ncbi.nlm.nih.gov/pubmed/29222512
http://dx.doi.org/10.1038/s41598-017-17143-1
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author Desai, Jigar S.
Sartor, Ryan C.
Lawas, Lovely Mae
Jagadish, S. V. Krishna
Doherty, Colleen J.
author_facet Desai, Jigar S.
Sartor, Ryan C.
Lawas, Lovely Mae
Jagadish, S. V. Krishna
Doherty, Colleen J.
author_sort Desai, Jigar S.
collection PubMed
description Organisms respond to changes in their environment through transcriptional regulatory networks (TRNs). The regulatory hierarchy of these networks can be inferred from expression data. Computational approaches to identify TRNs can be applied in any species where quality RNA can be acquired, However, ChIP-Seq and similar validation methods are challenging to employ in non-model species. Improving the accuracy of computational inference methods can significantly reduce the cost and time of subsequent validation experiments. We have developed ExRANGES, an approach that improves the ability to computationally infer TRN from time series expression data. ExRANGES utilizes both the rate of change in expression and the absolute expression level to identify TRN connections. We evaluated ExRANGES in five data sets from different model systems. ExRANGES improved the identification of experimentally validated transcription factor targets for all species tested, even in unevenly spaced and sparse data sets. This improved ability to predict known regulator-target relationships enhances the utility of network inference approaches in non-model species where experimental validation is challenging. We integrated ExRANGES with two different network construction approaches and it has been implemented as an R package available here: http://github.com/DohertyLab/ExRANGES. To install the package type: devtools::install_github(“DohertyLab/ExRANGES”).
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spelling pubmed-57229052017-12-12 Improving Gene Regulatory Network Inference by Incorporating Rates of Transcriptional Changes Desai, Jigar S. Sartor, Ryan C. Lawas, Lovely Mae Jagadish, S. V. Krishna Doherty, Colleen J. Sci Rep Article Organisms respond to changes in their environment through transcriptional regulatory networks (TRNs). The regulatory hierarchy of these networks can be inferred from expression data. Computational approaches to identify TRNs can be applied in any species where quality RNA can be acquired, However, ChIP-Seq and similar validation methods are challenging to employ in non-model species. Improving the accuracy of computational inference methods can significantly reduce the cost and time of subsequent validation experiments. We have developed ExRANGES, an approach that improves the ability to computationally infer TRN from time series expression data. ExRANGES utilizes both the rate of change in expression and the absolute expression level to identify TRN connections. We evaluated ExRANGES in five data sets from different model systems. ExRANGES improved the identification of experimentally validated transcription factor targets for all species tested, even in unevenly spaced and sparse data sets. This improved ability to predict known regulator-target relationships enhances the utility of network inference approaches in non-model species where experimental validation is challenging. We integrated ExRANGES with two different network construction approaches and it has been implemented as an R package available here: http://github.com/DohertyLab/ExRANGES. To install the package type: devtools::install_github(“DohertyLab/ExRANGES”). Nature Publishing Group UK 2017-12-08 /pmc/articles/PMC5722905/ /pubmed/29222512 http://dx.doi.org/10.1038/s41598-017-17143-1 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Desai, Jigar S.
Sartor, Ryan C.
Lawas, Lovely Mae
Jagadish, S. V. Krishna
Doherty, Colleen J.
Improving Gene Regulatory Network Inference by Incorporating Rates of Transcriptional Changes
title Improving Gene Regulatory Network Inference by Incorporating Rates of Transcriptional Changes
title_full Improving Gene Regulatory Network Inference by Incorporating Rates of Transcriptional Changes
title_fullStr Improving Gene Regulatory Network Inference by Incorporating Rates of Transcriptional Changes
title_full_unstemmed Improving Gene Regulatory Network Inference by Incorporating Rates of Transcriptional Changes
title_short Improving Gene Regulatory Network Inference by Incorporating Rates of Transcriptional Changes
title_sort improving gene regulatory network inference by incorporating rates of transcriptional changes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5722905/
https://www.ncbi.nlm.nih.gov/pubmed/29222512
http://dx.doi.org/10.1038/s41598-017-17143-1
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