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Shared origins of a key enzyme during the evolution of C(4) and CAM metabolism

CAM and C(4) photosynthesis are two key plant adaptations that have evolved independently multiple times, and are especially prevalent in particular groups of plants, including the Caryophyllales. We investigate the origin of photosynthetic PEPC, a key enzyme of both the CAM and C(4) pathways. We co...

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Autores principales: Christin, Pascal-Antoine, Arakaki, Monica, Osborne, Colin P., Bräutigam, Andrea, Sage, Rowan F., Hibberd, Julian M., Kelly, Steven, Covshoff, Sarah, Wong, Gane Ka-Shu, Hancock, Lillian, Edwards, Erika J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4085957/
https://www.ncbi.nlm.nih.gov/pubmed/24638902
http://dx.doi.org/10.1093/jxb/eru087
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author Christin, Pascal-Antoine
Arakaki, Monica
Osborne, Colin P.
Bräutigam, Andrea
Sage, Rowan F.
Hibberd, Julian M.
Kelly, Steven
Covshoff, Sarah
Wong, Gane Ka-Shu
Hancock, Lillian
Edwards, Erika J.
author_facet Christin, Pascal-Antoine
Arakaki, Monica
Osborne, Colin P.
Bräutigam, Andrea
Sage, Rowan F.
Hibberd, Julian M.
Kelly, Steven
Covshoff, Sarah
Wong, Gane Ka-Shu
Hancock, Lillian
Edwards, Erika J.
author_sort Christin, Pascal-Antoine
collection PubMed
description CAM and C(4) photosynthesis are two key plant adaptations that have evolved independently multiple times, and are especially prevalent in particular groups of plants, including the Caryophyllales. We investigate the origin of photosynthetic PEPC, a key enzyme of both the CAM and C(4) pathways. We combine phylogenetic analyses of genes encoding PEPC with analyses of RNA sequence data of Portulaca, the only plants known to perform both CAM and C(4) photosynthesis. Three distinct gene lineages encoding PEPC exist in eudicots (namely ppc-1E1, ppc-1E2 and ppc-2), one of which (ppc-1E1) was recurrently recruited for use in both CAM and C(4) photosynthesis within the Caryophyllales. This gene is present in multiple copies in the cacti and relatives, including Portulaca. The PEPC involved in the CAM and C(4) cycles of Portulaca are encoded by closely related yet distinct genes. The CAM-specific gene is similar to genes from related CAM taxa, suggesting that CAM has evolved before C(4) in these species. The similar origin of PEPC and other genes involved in the CAM and C(4) cycles highlights the shared early steps of evolutionary trajectories towards CAM and C(4), which probably diverged irreversibly only during the optimization of CAM and C(4) phenotypes.
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spelling pubmed-40859572014-07-10 Shared origins of a key enzyme during the evolution of C(4) and CAM metabolism Christin, Pascal-Antoine Arakaki, Monica Osborne, Colin P. Bräutigam, Andrea Sage, Rowan F. Hibberd, Julian M. Kelly, Steven Covshoff, Sarah Wong, Gane Ka-Shu Hancock, Lillian Edwards, Erika J. J Exp Bot Research Paper CAM and C(4) photosynthesis are two key plant adaptations that have evolved independently multiple times, and are especially prevalent in particular groups of plants, including the Caryophyllales. We investigate the origin of photosynthetic PEPC, a key enzyme of both the CAM and C(4) pathways. We combine phylogenetic analyses of genes encoding PEPC with analyses of RNA sequence data of Portulaca, the only plants known to perform both CAM and C(4) photosynthesis. Three distinct gene lineages encoding PEPC exist in eudicots (namely ppc-1E1, ppc-1E2 and ppc-2), one of which (ppc-1E1) was recurrently recruited for use in both CAM and C(4) photosynthesis within the Caryophyllales. This gene is present in multiple copies in the cacti and relatives, including Portulaca. The PEPC involved in the CAM and C(4) cycles of Portulaca are encoded by closely related yet distinct genes. The CAM-specific gene is similar to genes from related CAM taxa, suggesting that CAM has evolved before C(4) in these species. The similar origin of PEPC and other genes involved in the CAM and C(4) cycles highlights the shared early steps of evolutionary trajectories towards CAM and C(4), which probably diverged irreversibly only during the optimization of CAM and C(4) phenotypes. Oxford University Press 2014-07 2014-03-17 /pmc/articles/PMC4085957/ /pubmed/24638902 http://dx.doi.org/10.1093/jxb/eru087 Text en © The Author 2014. Published by Oxford University Press on behalf of the Society for Experimental Biology. http://creativecommons.org/licenses/by/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Paper
Christin, Pascal-Antoine
Arakaki, Monica
Osborne, Colin P.
Bräutigam, Andrea
Sage, Rowan F.
Hibberd, Julian M.
Kelly, Steven
Covshoff, Sarah
Wong, Gane Ka-Shu
Hancock, Lillian
Edwards, Erika J.
Shared origins of a key enzyme during the evolution of C(4) and CAM metabolism
title Shared origins of a key enzyme during the evolution of C(4) and CAM metabolism
title_full Shared origins of a key enzyme during the evolution of C(4) and CAM metabolism
title_fullStr Shared origins of a key enzyme during the evolution of C(4) and CAM metabolism
title_full_unstemmed Shared origins of a key enzyme during the evolution of C(4) and CAM metabolism
title_short Shared origins of a key enzyme during the evolution of C(4) and CAM metabolism
title_sort shared origins of a key enzyme during the evolution of c(4) and cam metabolism
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4085957/
https://www.ncbi.nlm.nih.gov/pubmed/24638902
http://dx.doi.org/10.1093/jxb/eru087
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