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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...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2014
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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. |
format | Online Article Text |
id | pubmed-4085957 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
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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