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The role of photorespiration during the evolution of C(4) photosynthesis in the genus Flaveria

C(4) photosynthesis represents a most remarkable case of convergent evolution of a complex trait, which includes the reprogramming of the expression patterns of thousands of genes. Anatomical, physiological, and phylogenetic and analyses as well as computational modeling indicate that the establishm...

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Autores principales: Mallmann, Julia, Heckmann, David, Bräutigam, Andrea, Lercher, Martin J, Weber, Andreas PM, Westhoff, Peter, Gowik, Udo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4103682/
https://www.ncbi.nlm.nih.gov/pubmed/24935935
http://dx.doi.org/10.7554/eLife.02478
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author Mallmann, Julia
Heckmann, David
Bräutigam, Andrea
Lercher, Martin J
Weber, Andreas PM
Westhoff, Peter
Gowik, Udo
author_facet Mallmann, Julia
Heckmann, David
Bräutigam, Andrea
Lercher, Martin J
Weber, Andreas PM
Westhoff, Peter
Gowik, Udo
author_sort Mallmann, Julia
collection PubMed
description C(4) photosynthesis represents a most remarkable case of convergent evolution of a complex trait, which includes the reprogramming of the expression patterns of thousands of genes. Anatomical, physiological, and phylogenetic and analyses as well as computational modeling indicate that the establishment of a photorespiratory carbon pump (termed C(2) photosynthesis) is a prerequisite for the evolution of C(4). However, a mechanistic model explaining the tight connection between the evolution of C(4) and C(2) photosynthesis is currently lacking. Here we address this question through comparative transcriptomic and biochemical analyses of closely related C(3), C(3)–C(4), and C(4) species, combined with Flux Balance Analysis constrained through a mechanistic model of carbon fixation. We show that C(2) photosynthesis creates a misbalance in nitrogen metabolism between bundle sheath and mesophyll cells. Rebalancing nitrogen metabolism requires anaplerotic reactions that resemble at least parts of a basic C(4) cycle. Our findings thus show how C(2) photosynthesis represents a pre-adaptation for the C(4) system, where the evolution of the C(2) system establishes important C(4) components as a side effect. DOI: http://dx.doi.org/10.7554/eLife.02478.001
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spelling pubmed-41036822014-07-22 The role of photorespiration during the evolution of C(4) photosynthesis in the genus Flaveria Mallmann, Julia Heckmann, David Bräutigam, Andrea Lercher, Martin J Weber, Andreas PM Westhoff, Peter Gowik, Udo eLife Genomics and Evolutionary Biology C(4) photosynthesis represents a most remarkable case of convergent evolution of a complex trait, which includes the reprogramming of the expression patterns of thousands of genes. Anatomical, physiological, and phylogenetic and analyses as well as computational modeling indicate that the establishment of a photorespiratory carbon pump (termed C(2) photosynthesis) is a prerequisite for the evolution of C(4). However, a mechanistic model explaining the tight connection between the evolution of C(4) and C(2) photosynthesis is currently lacking. Here we address this question through comparative transcriptomic and biochemical analyses of closely related C(3), C(3)–C(4), and C(4) species, combined with Flux Balance Analysis constrained through a mechanistic model of carbon fixation. We show that C(2) photosynthesis creates a misbalance in nitrogen metabolism between bundle sheath and mesophyll cells. Rebalancing nitrogen metabolism requires anaplerotic reactions that resemble at least parts of a basic C(4) cycle. Our findings thus show how C(2) photosynthesis represents a pre-adaptation for the C(4) system, where the evolution of the C(2) system establishes important C(4) components as a side effect. DOI: http://dx.doi.org/10.7554/eLife.02478.001 eLife Sciences Publications, Ltd 2014-06-16 /pmc/articles/PMC4103682/ /pubmed/24935935 http://dx.doi.org/10.7554/eLife.02478 Text en Copyright © 2014, Mallmann et al http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Genomics and Evolutionary Biology
Mallmann, Julia
Heckmann, David
Bräutigam, Andrea
Lercher, Martin J
Weber, Andreas PM
Westhoff, Peter
Gowik, Udo
The role of photorespiration during the evolution of C(4) photosynthesis in the genus Flaveria
title The role of photorespiration during the evolution of C(4) photosynthesis in the genus Flaveria
title_full The role of photorespiration during the evolution of C(4) photosynthesis in the genus Flaveria
title_fullStr The role of photorespiration during the evolution of C(4) photosynthesis in the genus Flaveria
title_full_unstemmed The role of photorespiration during the evolution of C(4) photosynthesis in the genus Flaveria
title_short The role of photorespiration during the evolution of C(4) photosynthesis in the genus Flaveria
title_sort role of photorespiration during the evolution of c(4) photosynthesis in the genus flaveria
topic Genomics and Evolutionary Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4103682/
https://www.ncbi.nlm.nih.gov/pubmed/24935935
http://dx.doi.org/10.7554/eLife.02478
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