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Analysis of companion cell and phloem metabolism using a transcriptome-guided model of Arabidopsis metabolism

Companion cells and sieve elements play an essential role in vascular plants, and yet the details of the metabolism that underpins their function remain largely unknown. Here, we construct a tissue-scale flux balance analysis (FBA) model to describe the metabolism of phloem loading in a mature Arabi...

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Autores principales: Hunt, Hilary, Brueggen, Nico, Galle, Alexander, Vanderauwera, Sandy, Frohberg, Claus, Fernie, Alisdair R, Sonnewald, Uwe, Sweetlove, Lee J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10231466/
https://www.ncbi.nlm.nih.gov/pubmed/36913519
http://dx.doi.org/10.1093/plphys/kiad154
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author Hunt, Hilary
Brueggen, Nico
Galle, Alexander
Vanderauwera, Sandy
Frohberg, Claus
Fernie, Alisdair R
Sonnewald, Uwe
Sweetlove, Lee J
author_facet Hunt, Hilary
Brueggen, Nico
Galle, Alexander
Vanderauwera, Sandy
Frohberg, Claus
Fernie, Alisdair R
Sonnewald, Uwe
Sweetlove, Lee J
author_sort Hunt, Hilary
collection PubMed
description Companion cells and sieve elements play an essential role in vascular plants, and yet the details of the metabolism that underpins their function remain largely unknown. Here, we construct a tissue-scale flux balance analysis (FBA) model to describe the metabolism of phloem loading in a mature Arabidopsis (Arabidopsis thaliana) leaf. We explore the potential metabolic interactions between mesophyll cells, companion cells, and sieve elements based on the current understanding of the physiology of phloem tissue and through the use of cell type–specific transcriptome data as a weighting in our model. We find that companion cell chloroplasts likely play a very different role to mesophyll chloroplasts. Our model suggests that, rather than carbon capture, the most crucial function of companion cell chloroplasts is to provide photosynthetically generated ATP to the cytosol. Additionally, our model predicts that the metabolites imported into the companion cell are not necessarily the same metabolites that are exported in phloem sap; phloem loading is more efficient if certain amino acids are synthesized in the phloem tissue. Surprisingly, in our model predictions, the proton-pumping pyrophosphatase (H(+)-PP(i)ase) is a more efficient contributor to the energization of the companion cell plasma membrane than the H(+)-ATPase.
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spelling pubmed-102314662023-06-01 Analysis of companion cell and phloem metabolism using a transcriptome-guided model of Arabidopsis metabolism Hunt, Hilary Brueggen, Nico Galle, Alexander Vanderauwera, Sandy Frohberg, Claus Fernie, Alisdair R Sonnewald, Uwe Sweetlove, Lee J Plant Physiol Research Article Companion cells and sieve elements play an essential role in vascular plants, and yet the details of the metabolism that underpins their function remain largely unknown. Here, we construct a tissue-scale flux balance analysis (FBA) model to describe the metabolism of phloem loading in a mature Arabidopsis (Arabidopsis thaliana) leaf. We explore the potential metabolic interactions between mesophyll cells, companion cells, and sieve elements based on the current understanding of the physiology of phloem tissue and through the use of cell type–specific transcriptome data as a weighting in our model. We find that companion cell chloroplasts likely play a very different role to mesophyll chloroplasts. Our model suggests that, rather than carbon capture, the most crucial function of companion cell chloroplasts is to provide photosynthetically generated ATP to the cytosol. Additionally, our model predicts that the metabolites imported into the companion cell are not necessarily the same metabolites that are exported in phloem sap; phloem loading is more efficient if certain amino acids are synthesized in the phloem tissue. Surprisingly, in our model predictions, the proton-pumping pyrophosphatase (H(+)-PP(i)ase) is a more efficient contributor to the energization of the companion cell plasma membrane than the H(+)-ATPase. Oxford University Press 2023-03-11 /pmc/articles/PMC10231466/ /pubmed/36913519 http://dx.doi.org/10.1093/plphys/kiad154 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of American Society of Plant Biologists. 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 Research Article
Hunt, Hilary
Brueggen, Nico
Galle, Alexander
Vanderauwera, Sandy
Frohberg, Claus
Fernie, Alisdair R
Sonnewald, Uwe
Sweetlove, Lee J
Analysis of companion cell and phloem metabolism using a transcriptome-guided model of Arabidopsis metabolism
title Analysis of companion cell and phloem metabolism using a transcriptome-guided model of Arabidopsis metabolism
title_full Analysis of companion cell and phloem metabolism using a transcriptome-guided model of Arabidopsis metabolism
title_fullStr Analysis of companion cell and phloem metabolism using a transcriptome-guided model of Arabidopsis metabolism
title_full_unstemmed Analysis of companion cell and phloem metabolism using a transcriptome-guided model of Arabidopsis metabolism
title_short Analysis of companion cell and phloem metabolism using a transcriptome-guided model of Arabidopsis metabolism
title_sort analysis of companion cell and phloem metabolism using a transcriptome-guided model of arabidopsis metabolism
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10231466/
https://www.ncbi.nlm.nih.gov/pubmed/36913519
http://dx.doi.org/10.1093/plphys/kiad154
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