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Hybrid analysis of gene dynamics predicts context-specific expression and offers regulatory insights
MOTIVATION: To understand the regulatory pathways underlying diseases, studies often investigate the differential gene expression between genetically or chemically differing cell populations. Differential expression analysis identifies global changes in transcription and enables the inference of fun...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6853664/ https://www.ncbi.nlm.nih.gov/pubmed/30994899 http://dx.doi.org/10.1093/bioinformatics/btz256 |
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author | Finkle, Justin D Bagheri, Neda |
author_facet | Finkle, Justin D Bagheri, Neda |
author_sort | Finkle, Justin D |
collection | PubMed |
description | MOTIVATION: To understand the regulatory pathways underlying diseases, studies often investigate the differential gene expression between genetically or chemically differing cell populations. Differential expression analysis identifies global changes in transcription and enables the inference of functional roles of applied perturbations. This approach has transformed the discovery of genetic drivers of disease and possible therapies. However, differential expression analysis does not provide quantitative predictions of gene expression in untested conditions. We present a hybrid approach, termed Differential Expression in Python (DiffExPy), that uniquely combines discrete, differential expression analysis with in silico differential equation simulations to yield accurate, quantitative predictions of gene expression from time-series data. RESULTS: To demonstrate the distinct insight provided by DiffExpy, we applied it to published, in vitro, time-series RNA-seq data from several genetic PI3K/PTEN variants of MCF10a cells stimulated with epidermal growth factor. DiffExPy proposed ensembles of several minimal differential equation systems for each differentially expressed gene. These systems provide quantitative models of expression for several previously uncharacterized genes and uncover new regulation by the PI3K/PTEN pathways. We validated model predictions on expression data from conditions that were not used for model training. Our discrete, differential expression analysis also identified SUZ12 and FOXA1 as possible regulators of specific groups of genes that exhibit late changes in expression. Our work reveals how DiffExPy generates quantitatively predictive models with testable, biological hypotheses from time-series expression data. AVAILABILITY AND IMPLEMENTATION: DiffExPy is available on GitHub (https://github.com/bagherilab/diffexpy). SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. |
format | Online Article Text |
id | pubmed-6853664 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-68536642019-11-19 Hybrid analysis of gene dynamics predicts context-specific expression and offers regulatory insights Finkle, Justin D Bagheri, Neda Bioinformatics Original Papers MOTIVATION: To understand the regulatory pathways underlying diseases, studies often investigate the differential gene expression between genetically or chemically differing cell populations. Differential expression analysis identifies global changes in transcription and enables the inference of functional roles of applied perturbations. This approach has transformed the discovery of genetic drivers of disease and possible therapies. However, differential expression analysis does not provide quantitative predictions of gene expression in untested conditions. We present a hybrid approach, termed Differential Expression in Python (DiffExPy), that uniquely combines discrete, differential expression analysis with in silico differential equation simulations to yield accurate, quantitative predictions of gene expression from time-series data. RESULTS: To demonstrate the distinct insight provided by DiffExpy, we applied it to published, in vitro, time-series RNA-seq data from several genetic PI3K/PTEN variants of MCF10a cells stimulated with epidermal growth factor. DiffExPy proposed ensembles of several minimal differential equation systems for each differentially expressed gene. These systems provide quantitative models of expression for several previously uncharacterized genes and uncover new regulation by the PI3K/PTEN pathways. We validated model predictions on expression data from conditions that were not used for model training. Our discrete, differential expression analysis also identified SUZ12 and FOXA1 as possible regulators of specific groups of genes that exhibit late changes in expression. Our work reveals how DiffExPy generates quantitatively predictive models with testable, biological hypotheses from time-series expression data. AVAILABILITY AND IMPLEMENTATION: DiffExPy is available on GitHub (https://github.com/bagherilab/diffexpy). SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. Oxford University Press 2019-11-15 2019-04-17 /pmc/articles/PMC6853664/ /pubmed/30994899 http://dx.doi.org/10.1093/bioinformatics/btz256 Text en © The Author(s) 2019. Published by Oxford University Press. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Papers Finkle, Justin D Bagheri, Neda Hybrid analysis of gene dynamics predicts context-specific expression and offers regulatory insights |
title | Hybrid analysis of gene dynamics predicts context-specific expression and offers regulatory insights |
title_full | Hybrid analysis of gene dynamics predicts context-specific expression and offers regulatory insights |
title_fullStr | Hybrid analysis of gene dynamics predicts context-specific expression and offers regulatory insights |
title_full_unstemmed | Hybrid analysis of gene dynamics predicts context-specific expression and offers regulatory insights |
title_short | Hybrid analysis of gene dynamics predicts context-specific expression and offers regulatory insights |
title_sort | hybrid analysis of gene dynamics predicts context-specific expression and offers regulatory insights |
topic | Original Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6853664/ https://www.ncbi.nlm.nih.gov/pubmed/30994899 http://dx.doi.org/10.1093/bioinformatics/btz256 |
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