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Transcriptome integrated metabolic modeling of carbon assimilation underlying storage root development in cassava
The existing genome-scale metabolic model of carbon metabolism in cassava storage roots, rMeCBM, has proven particularly resourceful in exploring the metabolic basis for the phenotypic differences between high and low-yield cassava cultivars. However, experimental validation of predicted metabolic f...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8062692/ https://www.ncbi.nlm.nih.gov/pubmed/33888810 http://dx.doi.org/10.1038/s41598-021-88129-3 |
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author | Kamsen, Ratchaprapa Kalapanulak, Saowalak Chiewchankaset, Porntip Saithong, Treenut |
author_facet | Kamsen, Ratchaprapa Kalapanulak, Saowalak Chiewchankaset, Porntip Saithong, Treenut |
author_sort | Kamsen, Ratchaprapa |
collection | PubMed |
description | The existing genome-scale metabolic model of carbon metabolism in cassava storage roots, rMeCBM, has proven particularly resourceful in exploring the metabolic basis for the phenotypic differences between high and low-yield cassava cultivars. However, experimental validation of predicted metabolic fluxes by carbon labeling is quite challenging. Here, we incorporated gene expression data of developing storage roots into the basic flux-balance model to minimize infeasible metabolic fluxes, denoted as rMeCBMx, thereby improving the plausibility of the simulation and predictive power. Three different conceptual algorithms, GIMME, E-Flux, and HPCOF were evaluated. The rMeCBMx-HPCOF model outperformed others in predicting carbon fluxes in the metabolism of storage roots and, in particular, was highly consistent with transcriptome of high-yield cultivars. The flux prediction was improved through the oxidative pentose phosphate pathway in cytosol, as has been reported in various studies on root metabolism, but hardly captured by simple FBA models. Moreover, the presence of fluxes through cytosolic glycolysis and alanine biosynthesis pathways were predicted with high consistency with gene expression levels. This study sheds light on the importance of prediction power in the modeling of complex plant metabolism. Integration of multi-omics data would further help mitigate the ill-posed problem of constraint-based modeling, allowing more realistic simulation. |
format | Online Article Text |
id | pubmed-8062692 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-80626922021-04-27 Transcriptome integrated metabolic modeling of carbon assimilation underlying storage root development in cassava Kamsen, Ratchaprapa Kalapanulak, Saowalak Chiewchankaset, Porntip Saithong, Treenut Sci Rep Article The existing genome-scale metabolic model of carbon metabolism in cassava storage roots, rMeCBM, has proven particularly resourceful in exploring the metabolic basis for the phenotypic differences between high and low-yield cassava cultivars. However, experimental validation of predicted metabolic fluxes by carbon labeling is quite challenging. Here, we incorporated gene expression data of developing storage roots into the basic flux-balance model to minimize infeasible metabolic fluxes, denoted as rMeCBMx, thereby improving the plausibility of the simulation and predictive power. Three different conceptual algorithms, GIMME, E-Flux, and HPCOF were evaluated. The rMeCBMx-HPCOF model outperformed others in predicting carbon fluxes in the metabolism of storage roots and, in particular, was highly consistent with transcriptome of high-yield cultivars. The flux prediction was improved through the oxidative pentose phosphate pathway in cytosol, as has been reported in various studies on root metabolism, but hardly captured by simple FBA models. Moreover, the presence of fluxes through cytosolic glycolysis and alanine biosynthesis pathways were predicted with high consistency with gene expression levels. This study sheds light on the importance of prediction power in the modeling of complex plant metabolism. Integration of multi-omics data would further help mitigate the ill-posed problem of constraint-based modeling, allowing more realistic simulation. Nature Publishing Group UK 2021-04-22 /pmc/articles/PMC8062692/ /pubmed/33888810 http://dx.doi.org/10.1038/s41598-021-88129-3 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Kamsen, Ratchaprapa Kalapanulak, Saowalak Chiewchankaset, Porntip Saithong, Treenut Transcriptome integrated metabolic modeling of carbon assimilation underlying storage root development in cassava |
title | Transcriptome integrated metabolic modeling of carbon assimilation underlying storage root development in cassava |
title_full | Transcriptome integrated metabolic modeling of carbon assimilation underlying storage root development in cassava |
title_fullStr | Transcriptome integrated metabolic modeling of carbon assimilation underlying storage root development in cassava |
title_full_unstemmed | Transcriptome integrated metabolic modeling of carbon assimilation underlying storage root development in cassava |
title_short | Transcriptome integrated metabolic modeling of carbon assimilation underlying storage root development in cassava |
title_sort | transcriptome integrated metabolic modeling of carbon assimilation underlying storage root development in cassava |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8062692/ https://www.ncbi.nlm.nih.gov/pubmed/33888810 http://dx.doi.org/10.1038/s41598-021-88129-3 |
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