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Evidence for adaptive evolution of low-temperature stress response genes in a Pooideae grass ancestor
Adaptation to temperate environments is common in the grass subfamily Pooideae, suggesting an ancestral origin of cold climate adaptation. Here, we investigated substitution rates of genes involved in low-temperature-induced (LTI) stress responses to test the hypothesis that adaptive molecular evolu...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3840698/ https://www.ncbi.nlm.nih.gov/pubmed/23701123 http://dx.doi.org/10.1111/nph.12337 |
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author | Vigeland, Magnus D Spannagl, Manuel Asp, Torben Paina, Cristiana Rudi, Heidi Rognli, Odd-Arne Fjellheim, Siri Sandve, Simen R |
author_facet | Vigeland, Magnus D Spannagl, Manuel Asp, Torben Paina, Cristiana Rudi, Heidi Rognli, Odd-Arne Fjellheim, Siri Sandve, Simen R |
author_sort | Vigeland, Magnus D |
collection | PubMed |
description | Adaptation to temperate environments is common in the grass subfamily Pooideae, suggesting an ancestral origin of cold climate adaptation. Here, we investigated substitution rates of genes involved in low-temperature-induced (LTI) stress responses to test the hypothesis that adaptive molecular evolution of LTI pathway genes was important for Pooideae evolution. Substitution rates and signatures of positive selection were analyzed using 4330 gene trees including three warm climate-adapted species (maize (Zea mays), sorghum (Sorghum bicolor), and rice (Oryza sativa)) and five temperate Pooideae species (Brachypodium distachyon, wheat (Triticum aestivum), barley (Hordeum vulgare), Lolium perenne and Festuca pratensis). Nonsynonymous substitution rate differences between Pooideae and warm habitat-adapted species were elevated in LTI trees compared with all trees. Furthermore, signatures of positive selection were significantly stronger in LTI trees after the rice and Pooideae split but before the Brachypodium divergence (P < 0.05). Genome-wide heterogeneity in substitution rates was also observed, reflecting divergent genome evolution processes within these grasses. Our results provide evidence for a link between adaptation to cold habitats and adaptive evolution of LTI stress responses in early Pooideae evolution and shed light on a poorly understood chapter in the evolutionary history of some of the world's most important temperate crops. |
format | Online Article Text |
id | pubmed-3840698 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Blackwell Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-38406982013-12-02 Evidence for adaptive evolution of low-temperature stress response genes in a Pooideae grass ancestor Vigeland, Magnus D Spannagl, Manuel Asp, Torben Paina, Cristiana Rudi, Heidi Rognli, Odd-Arne Fjellheim, Siri Sandve, Simen R New Phytol Research Adaptation to temperate environments is common in the grass subfamily Pooideae, suggesting an ancestral origin of cold climate adaptation. Here, we investigated substitution rates of genes involved in low-temperature-induced (LTI) stress responses to test the hypothesis that adaptive molecular evolution of LTI pathway genes was important for Pooideae evolution. Substitution rates and signatures of positive selection were analyzed using 4330 gene trees including three warm climate-adapted species (maize (Zea mays), sorghum (Sorghum bicolor), and rice (Oryza sativa)) and five temperate Pooideae species (Brachypodium distachyon, wheat (Triticum aestivum), barley (Hordeum vulgare), Lolium perenne and Festuca pratensis). Nonsynonymous substitution rate differences between Pooideae and warm habitat-adapted species were elevated in LTI trees compared with all trees. Furthermore, signatures of positive selection were significantly stronger in LTI trees after the rice and Pooideae split but before the Brachypodium divergence (P < 0.05). Genome-wide heterogeneity in substitution rates was also observed, reflecting divergent genome evolution processes within these grasses. Our results provide evidence for a link between adaptation to cold habitats and adaptive evolution of LTI stress responses in early Pooideae evolution and shed light on a poorly understood chapter in the evolutionary history of some of the world's most important temperate crops. Blackwell Publishing 2013-09 2013-05-23 /pmc/articles/PMC3840698/ /pubmed/23701123 http://dx.doi.org/10.1111/nph.12337 Text en Copyright © 2013 New Phytologist Trust http://creativecommons.org/licenses/by/2.5/ Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation. |
spellingShingle | Research Vigeland, Magnus D Spannagl, Manuel Asp, Torben Paina, Cristiana Rudi, Heidi Rognli, Odd-Arne Fjellheim, Siri Sandve, Simen R Evidence for adaptive evolution of low-temperature stress response genes in a Pooideae grass ancestor |
title | Evidence for adaptive evolution of low-temperature stress response genes in a Pooideae grass ancestor |
title_full | Evidence for adaptive evolution of low-temperature stress response genes in a Pooideae grass ancestor |
title_fullStr | Evidence for adaptive evolution of low-temperature stress response genes in a Pooideae grass ancestor |
title_full_unstemmed | Evidence for adaptive evolution of low-temperature stress response genes in a Pooideae grass ancestor |
title_short | Evidence for adaptive evolution of low-temperature stress response genes in a Pooideae grass ancestor |
title_sort | evidence for adaptive evolution of low-temperature stress response genes in a pooideae grass ancestor |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3840698/ https://www.ncbi.nlm.nih.gov/pubmed/23701123 http://dx.doi.org/10.1111/nph.12337 |
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