Cargando…
Adaptive evolution and divergent expression of heat stress transcription factors in grasses
BACKGROUND: Heat stress transcription factors (Hsfs) regulate gene expression in response to heat and many other environmental stresses in plants. Understanding the adaptive evolution of Hsf genes in the grass family will provide potentially useful information for the genetic improvement of modern c...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4094458/ https://www.ncbi.nlm.nih.gov/pubmed/24974883 http://dx.doi.org/10.1186/1471-2148-14-147 |
_version_ | 1782325830813220864 |
---|---|
author | Yang, Zefeng Wang, Yifan Gao, Yun Zhou, Yong Zhang, Enying Hu, Yunyun Yuan, Yuan Liang, Guohua Xu, Chenwu |
author_facet | Yang, Zefeng Wang, Yifan Gao, Yun Zhou, Yong Zhang, Enying Hu, Yunyun Yuan, Yuan Liang, Guohua Xu, Chenwu |
author_sort | Yang, Zefeng |
collection | PubMed |
description | BACKGROUND: Heat stress transcription factors (Hsfs) regulate gene expression in response to heat and many other environmental stresses in plants. Understanding the adaptive evolution of Hsf genes in the grass family will provide potentially useful information for the genetic improvement of modern crops to handle increasing global temperatures. RESULTS: In this work, we performed a genome-wide survey of Hsf genes in 5 grass species, including rice, maize, sorghum, Setaria, and Brachypodium, by describing their phylogenetic relationships, adaptive evolution, and expression patterns under abiotic stresses. The Hsf genes in grasses were divided into 24 orthologous gene clusters (OGCs) based on phylogeneitc relationship and synteny, suggesting that 24 Hsf genes were present in the ancestral grass genome. However, 9 duplication and 4 gene-loss events were identified in the tested genomes. A maximum-likelihood analysis revealed the effects of positive selection in the evolution of 11 OGCs and suggested that OGCs with duplicated or lost genes were more readily influenced by positive selection than other OGCs. Further investigation revealed that positive selection acted on only one of the duplicated genes in 8 of 9 paralogous pairs, suggesting that neofunctionalization contributed to the evolution of these duplicated pairs. We also investigated the expression patterns of rice and maize Hsf genes under heat, salt, drought, and cold stresses. The results revealed divergent expression patterns between the duplicated genes. CONCLUSIONS: This study demonstrates that neofunctionalization by changes in expression pattern and function following gene duplication has been an important factor in the maintenance and divergence of grass Hsf genes. |
format | Online Article Text |
id | pubmed-4094458 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-40944582014-07-23 Adaptive evolution and divergent expression of heat stress transcription factors in grasses Yang, Zefeng Wang, Yifan Gao, Yun Zhou, Yong Zhang, Enying Hu, Yunyun Yuan, Yuan Liang, Guohua Xu, Chenwu BMC Evol Biol Research Article BACKGROUND: Heat stress transcription factors (Hsfs) regulate gene expression in response to heat and many other environmental stresses in plants. Understanding the adaptive evolution of Hsf genes in the grass family will provide potentially useful information for the genetic improvement of modern crops to handle increasing global temperatures. RESULTS: In this work, we performed a genome-wide survey of Hsf genes in 5 grass species, including rice, maize, sorghum, Setaria, and Brachypodium, by describing their phylogenetic relationships, adaptive evolution, and expression patterns under abiotic stresses. The Hsf genes in grasses were divided into 24 orthologous gene clusters (OGCs) based on phylogeneitc relationship and synteny, suggesting that 24 Hsf genes were present in the ancestral grass genome. However, 9 duplication and 4 gene-loss events were identified in the tested genomes. A maximum-likelihood analysis revealed the effects of positive selection in the evolution of 11 OGCs and suggested that OGCs with duplicated or lost genes were more readily influenced by positive selection than other OGCs. Further investigation revealed that positive selection acted on only one of the duplicated genes in 8 of 9 paralogous pairs, suggesting that neofunctionalization contributed to the evolution of these duplicated pairs. We also investigated the expression patterns of rice and maize Hsf genes under heat, salt, drought, and cold stresses. The results revealed divergent expression patterns between the duplicated genes. CONCLUSIONS: This study demonstrates that neofunctionalization by changes in expression pattern and function following gene duplication has been an important factor in the maintenance and divergence of grass Hsf genes. BioMed Central 2014-06-30 /pmc/articles/PMC4094458/ /pubmed/24974883 http://dx.doi.org/10.1186/1471-2148-14-147 Text en Copyright © 2014 Yang et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. |
spellingShingle | Research Article Yang, Zefeng Wang, Yifan Gao, Yun Zhou, Yong Zhang, Enying Hu, Yunyun Yuan, Yuan Liang, Guohua Xu, Chenwu Adaptive evolution and divergent expression of heat stress transcription factors in grasses |
title | Adaptive evolution and divergent expression of heat stress transcription factors in grasses |
title_full | Adaptive evolution and divergent expression of heat stress transcription factors in grasses |
title_fullStr | Adaptive evolution and divergent expression of heat stress transcription factors in grasses |
title_full_unstemmed | Adaptive evolution and divergent expression of heat stress transcription factors in grasses |
title_short | Adaptive evolution and divergent expression of heat stress transcription factors in grasses |
title_sort | adaptive evolution and divergent expression of heat stress transcription factors in grasses |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4094458/ https://www.ncbi.nlm.nih.gov/pubmed/24974883 http://dx.doi.org/10.1186/1471-2148-14-147 |
work_keys_str_mv | AT yangzefeng adaptiveevolutionanddivergentexpressionofheatstresstranscriptionfactorsingrasses AT wangyifan adaptiveevolutionanddivergentexpressionofheatstresstranscriptionfactorsingrasses AT gaoyun adaptiveevolutionanddivergentexpressionofheatstresstranscriptionfactorsingrasses AT zhouyong adaptiveevolutionanddivergentexpressionofheatstresstranscriptionfactorsingrasses AT zhangenying adaptiveevolutionanddivergentexpressionofheatstresstranscriptionfactorsingrasses AT huyunyun adaptiveevolutionanddivergentexpressionofheatstresstranscriptionfactorsingrasses AT yuanyuan adaptiveevolutionanddivergentexpressionofheatstresstranscriptionfactorsingrasses AT liangguohua adaptiveevolutionanddivergentexpressionofheatstresstranscriptionfactorsingrasses AT xuchenwu adaptiveevolutionanddivergentexpressionofheatstresstranscriptionfactorsingrasses |