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Unusual tandem expansion and positive selection in subgroups of the plant GRAS transcription factor superfamily
BACKGROUND: GRAS proteins belong to a plant transcription factor family that is involved with multifarious roles in plants. Although previous studies of this protein family have been reported for Arabidopsis, rice, Chinese cabbage and other species, investigation of expansion patterns and evolutiona...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4279901/ https://www.ncbi.nlm.nih.gov/pubmed/25524588 http://dx.doi.org/10.1186/s12870-014-0373-5 |
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author | Wu, Ningning Zhu, Yan Song, Wanlu Li, Yaxuan Yan, Yueming Hu, Yingkao |
author_facet | Wu, Ningning Zhu, Yan Song, Wanlu Li, Yaxuan Yan, Yueming Hu, Yingkao |
author_sort | Wu, Ningning |
collection | PubMed |
description | BACKGROUND: GRAS proteins belong to a plant transcription factor family that is involved with multifarious roles in plants. Although previous studies of this protein family have been reported for Arabidopsis, rice, Chinese cabbage and other species, investigation of expansion patterns and evolutionary rate on the basis of comparative genomics in different species remains inadequate. RESULTS: A total of 289 GRAS genes were identified in Arabidopsis, B. distachyon, rice, soybean, S. moellendorffii, and P. patens and were grouped into seven subfamilies, supported by the similarity of their exon–intron patterns and structural motifs. All of tandem duplicated genes were found in group II except one cluster of rice, indicating that tandem duplication greatly promoted the expansion of group II. Furthermore, segment duplications were mainly found in the soybean genome, whereas no single expansion pattern dominated in other plant species indicating that GRAS genes from these five species might be subject to a more complex evolutionary mechanism. Interestingly, branch-site model analyses of positive selection showed that a number of sites were positively selected under foreground branches I and V. These results strongly indicated that these groups were experiencing higher positive selection pressure. Meanwhile, the site-specific model revealed that the GRAS genes were under strong positive selection in P. patens. DIVERGE v2.0 was used to detect critical amino acid sites, and the results showed that the shifted evolutionary rate was mainly attributed to the functional divergence between the GRAS genes in the two groups. In addition, the results also demonstrated the expression divergence of the GRAS duplicated genes in the evolution. In short, the results above provide a solid foundation for further functional dissection of the GRAS gene superfamily. CONCLUSIONS: In this work, differential expression, evolutionary rate, and expansion patterns of the GRAS gene family in the six species were predicted. Especially, tandem duplication events played an important role in expansion of group II. Together, these results contribute to further functional analysis and the molecular evolution of the GRAS gene superfamily. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12870-014-0373-5) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4279901 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-42799012014-12-31 Unusual tandem expansion and positive selection in subgroups of the plant GRAS transcription factor superfamily Wu, Ningning Zhu, Yan Song, Wanlu Li, Yaxuan Yan, Yueming Hu, Yingkao BMC Plant Biol Research Article BACKGROUND: GRAS proteins belong to a plant transcription factor family that is involved with multifarious roles in plants. Although previous studies of this protein family have been reported for Arabidopsis, rice, Chinese cabbage and other species, investigation of expansion patterns and evolutionary rate on the basis of comparative genomics in different species remains inadequate. RESULTS: A total of 289 GRAS genes were identified in Arabidopsis, B. distachyon, rice, soybean, S. moellendorffii, and P. patens and were grouped into seven subfamilies, supported by the similarity of their exon–intron patterns and structural motifs. All of tandem duplicated genes were found in group II except one cluster of rice, indicating that tandem duplication greatly promoted the expansion of group II. Furthermore, segment duplications were mainly found in the soybean genome, whereas no single expansion pattern dominated in other plant species indicating that GRAS genes from these five species might be subject to a more complex evolutionary mechanism. Interestingly, branch-site model analyses of positive selection showed that a number of sites were positively selected under foreground branches I and V. These results strongly indicated that these groups were experiencing higher positive selection pressure. Meanwhile, the site-specific model revealed that the GRAS genes were under strong positive selection in P. patens. DIVERGE v2.0 was used to detect critical amino acid sites, and the results showed that the shifted evolutionary rate was mainly attributed to the functional divergence between the GRAS genes in the two groups. In addition, the results also demonstrated the expression divergence of the GRAS duplicated genes in the evolution. In short, the results above provide a solid foundation for further functional dissection of the GRAS gene superfamily. CONCLUSIONS: In this work, differential expression, evolutionary rate, and expansion patterns of the GRAS gene family in the six species were predicted. Especially, tandem duplication events played an important role in expansion of group II. Together, these results contribute to further functional analysis and the molecular evolution of the GRAS gene superfamily. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12870-014-0373-5) contains supplementary material, which is available to authorized users. BioMed Central 2014-12-19 /pmc/articles/PMC4279901/ /pubmed/25524588 http://dx.doi.org/10.1186/s12870-014-0373-5 Text en © Wu et al.; licensee BioMed Central. 2014 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Wu, Ningning Zhu, Yan Song, Wanlu Li, Yaxuan Yan, Yueming Hu, Yingkao Unusual tandem expansion and positive selection in subgroups of the plant GRAS transcription factor superfamily |
title | Unusual tandem expansion and positive selection in subgroups of the plant GRAS transcription factor superfamily |
title_full | Unusual tandem expansion and positive selection in subgroups of the plant GRAS transcription factor superfamily |
title_fullStr | Unusual tandem expansion and positive selection in subgroups of the plant GRAS transcription factor superfamily |
title_full_unstemmed | Unusual tandem expansion and positive selection in subgroups of the plant GRAS transcription factor superfamily |
title_short | Unusual tandem expansion and positive selection in subgroups of the plant GRAS transcription factor superfamily |
title_sort | unusual tandem expansion and positive selection in subgroups of the plant gras transcription factor superfamily |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4279901/ https://www.ncbi.nlm.nih.gov/pubmed/25524588 http://dx.doi.org/10.1186/s12870-014-0373-5 |
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