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Accurate flux predictions using tissue-specific gene expression in plant metabolic modeling
MOTIVATION: The accurate prediction of complex phenotypes such as metabolic fluxes in living systems is a grand challenge for systems biology and central to efficiently identifying biotechnological interventions that can address pressing industrial needs. The application of gene expression data to i...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10159652/ https://www.ncbi.nlm.nih.gov/pubmed/37040081 http://dx.doi.org/10.1093/bioinformatics/btad186 |
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author | Kaste, Joshua A M Shachar-Hill, Yair |
author_facet | Kaste, Joshua A M Shachar-Hill, Yair |
author_sort | Kaste, Joshua A M |
collection | PubMed |
description | MOTIVATION: The accurate prediction of complex phenotypes such as metabolic fluxes in living systems is a grand challenge for systems biology and central to efficiently identifying biotechnological interventions that can address pressing industrial needs. The application of gene expression data to improve the accuracy of metabolic flux predictions using mechanistic modeling methods such as flux balance analysis (FBA) has not been previously demonstrated in multi-tissue systems, despite their biotechnological importance. We hypothesized that a method for generating metabolic flux predictions informed by relative expression levels between tissues would improve prediction accuracy. RESULTS: Relative gene expression levels derived from multiple transcriptomic and proteomic datasets were integrated into FBA predictions of a multi-tissue, diel model of Arabidopsis thaliana’s central metabolism. This integration dramatically improved the agreement of flux predictions with experimentally based flux maps from (13)C metabolic flux analysis compared with a standard parsimonious FBA approach. Disagreement between FBA predictions and MFA flux maps was measured using weighted averaged percent error values, and for parsimonious FBA this was169%–180% for high light conditions and 94%–103% for low light conditions, depending on the gene expression dataset used. This fell to 10%-13% and 9%-11% upon incorporating expression data into the modeling process, which also substantially altered the predicted carbon and energy economy of the plant. AVAILABILITY AND IMPLEMENTATION: Code and data generated as part of this study are available from https://github.com/Gibberella/ArabidopsisGeneExpressionWeights. |
format | Online Article Text |
id | pubmed-10159652 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-101596522023-05-05 Accurate flux predictions using tissue-specific gene expression in plant metabolic modeling Kaste, Joshua A M Shachar-Hill, Yair Bioinformatics Original Paper MOTIVATION: The accurate prediction of complex phenotypes such as metabolic fluxes in living systems is a grand challenge for systems biology and central to efficiently identifying biotechnological interventions that can address pressing industrial needs. The application of gene expression data to improve the accuracy of metabolic flux predictions using mechanistic modeling methods such as flux balance analysis (FBA) has not been previously demonstrated in multi-tissue systems, despite their biotechnological importance. We hypothesized that a method for generating metabolic flux predictions informed by relative expression levels between tissues would improve prediction accuracy. RESULTS: Relative gene expression levels derived from multiple transcriptomic and proteomic datasets were integrated into FBA predictions of a multi-tissue, diel model of Arabidopsis thaliana’s central metabolism. This integration dramatically improved the agreement of flux predictions with experimentally based flux maps from (13)C metabolic flux analysis compared with a standard parsimonious FBA approach. Disagreement between FBA predictions and MFA flux maps was measured using weighted averaged percent error values, and for parsimonious FBA this was169%–180% for high light conditions and 94%–103% for low light conditions, depending on the gene expression dataset used. This fell to 10%-13% and 9%-11% upon incorporating expression data into the modeling process, which also substantially altered the predicted carbon and energy economy of the plant. AVAILABILITY AND IMPLEMENTATION: Code and data generated as part of this study are available from https://github.com/Gibberella/ArabidopsisGeneExpressionWeights. Oxford University Press 2023-04-11 /pmc/articles/PMC10159652/ /pubmed/37040081 http://dx.doi.org/10.1093/bioinformatics/btad186 Text en © The Author(s) 2023. Published by Oxford University Press. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://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 Paper Kaste, Joshua A M Shachar-Hill, Yair Accurate flux predictions using tissue-specific gene expression in plant metabolic modeling |
title | Accurate flux predictions using tissue-specific gene expression in plant metabolic modeling |
title_full | Accurate flux predictions using tissue-specific gene expression in plant metabolic modeling |
title_fullStr | Accurate flux predictions using tissue-specific gene expression in plant metabolic modeling |
title_full_unstemmed | Accurate flux predictions using tissue-specific gene expression in plant metabolic modeling |
title_short | Accurate flux predictions using tissue-specific gene expression in plant metabolic modeling |
title_sort | accurate flux predictions using tissue-specific gene expression in plant metabolic modeling |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10159652/ https://www.ncbi.nlm.nih.gov/pubmed/37040081 http://dx.doi.org/10.1093/bioinformatics/btad186 |
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