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Genome-wide analysis of OSCA gene family members in Vigna radiata and their involvement in the osmotic response

BACKGROUND: Mung bean (Vigna radiata) is a warm-season legume crop and belongs to the papilionoid subfamily of the Fabaceae family. China is the leading producer of mung bean in the world. Mung bean has significant economic and health benefits and is a promising species with broad adaptation ability...

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Autores principales: Yin, Lili, Zhang, Meiling, Wu, Ruigang, Chen, Xiaoliang, Liu, Fei, Xing, Baolong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8422765/
https://www.ncbi.nlm.nih.gov/pubmed/34493199
http://dx.doi.org/10.1186/s12870-021-03184-2
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author Yin, Lili
Zhang, Meiling
Wu, Ruigang
Chen, Xiaoliang
Liu, Fei
Xing, Baolong
author_facet Yin, Lili
Zhang, Meiling
Wu, Ruigang
Chen, Xiaoliang
Liu, Fei
Xing, Baolong
author_sort Yin, Lili
collection PubMed
description BACKGROUND: Mung bean (Vigna radiata) is a warm-season legume crop and belongs to the papilionoid subfamily of the Fabaceae family. China is the leading producer of mung bean in the world. Mung bean has significant economic and health benefits and is a promising species with broad adaptation ability and high tolerance to environmental stresses. OSCA (hyperosmolality-gated calcium-permeable channel) gene family members play an important role in the modulation of hypertonic stress, such as drought and salinity. However, genome-wide analysis of the OSCA gene family has not been conducted in mung bean. RESULTS: We identified a total of 13 OSCA genes in the mung bean genome and named them according to their homology with AtOSCAs. All the OSCAs were phylogenetically split into four clades. Phylogenetic relationship and synteny analyses showed that the VrOSCAs in mung bean and soybean shared a relatively conserved evolutionary history. In addition, three duplicated VrOSCA gene pairs were identified, and the duplicated VrOSCAs gene pairs mainly underwent purifying selection pressure during evolution. Protein domain, motif and transmembrane analyses indicated that most of the VrOSCAs shared similar structures with their homologs. The expression pattern showed that except for VrOSCA2.1, the other 12 VrOSCAs were upregulated under treatment with ABA, PEG and NaCl, among which VrOSCA1.4 showed the largest increased expression levels. The duplicated genes VrOSCA2.1/VrOSCA2.2 showed divergent expression, which might have resulted in functionalization during subsequent evolution. The expression profiles under ABA, PEG and NaCl stress revealed a functional divergence of VrOSCA genes, which agreed with the analysis of cis-acting regulatory elements in the promoter regions of VrOSCA genes. CONCLUSIONS: Collectively, the study provided a systematic analysis of the VrOSCA gene family in mung bean. Our results establish an important foundation for functional and evolutionary analysis of VrOSCAs and identify genes for further investigation of their ability to confer abiotic stress tolerance in mung bean. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12870-021-03184-2.
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spelling pubmed-84227652021-09-09 Genome-wide analysis of OSCA gene family members in Vigna radiata and their involvement in the osmotic response Yin, Lili Zhang, Meiling Wu, Ruigang Chen, Xiaoliang Liu, Fei Xing, Baolong BMC Plant Biol Research Article BACKGROUND: Mung bean (Vigna radiata) is a warm-season legume crop and belongs to the papilionoid subfamily of the Fabaceae family. China is the leading producer of mung bean in the world. Mung bean has significant economic and health benefits and is a promising species with broad adaptation ability and high tolerance to environmental stresses. OSCA (hyperosmolality-gated calcium-permeable channel) gene family members play an important role in the modulation of hypertonic stress, such as drought and salinity. However, genome-wide analysis of the OSCA gene family has not been conducted in mung bean. RESULTS: We identified a total of 13 OSCA genes in the mung bean genome and named them according to their homology with AtOSCAs. All the OSCAs were phylogenetically split into four clades. Phylogenetic relationship and synteny analyses showed that the VrOSCAs in mung bean and soybean shared a relatively conserved evolutionary history. In addition, three duplicated VrOSCA gene pairs were identified, and the duplicated VrOSCAs gene pairs mainly underwent purifying selection pressure during evolution. Protein domain, motif and transmembrane analyses indicated that most of the VrOSCAs shared similar structures with their homologs. The expression pattern showed that except for VrOSCA2.1, the other 12 VrOSCAs were upregulated under treatment with ABA, PEG and NaCl, among which VrOSCA1.4 showed the largest increased expression levels. The duplicated genes VrOSCA2.1/VrOSCA2.2 showed divergent expression, which might have resulted in functionalization during subsequent evolution. The expression profiles under ABA, PEG and NaCl stress revealed a functional divergence of VrOSCA genes, which agreed with the analysis of cis-acting regulatory elements in the promoter regions of VrOSCA genes. CONCLUSIONS: Collectively, the study provided a systematic analysis of the VrOSCA gene family in mung bean. Our results establish an important foundation for functional and evolutionary analysis of VrOSCAs and identify genes for further investigation of their ability to confer abiotic stress tolerance in mung bean. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12870-021-03184-2. BioMed Central 2021-09-07 /pmc/articles/PMC8422765/ /pubmed/34493199 http://dx.doi.org/10.1186/s12870-021-03184-2 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Yin, Lili
Zhang, Meiling
Wu, Ruigang
Chen, Xiaoliang
Liu, Fei
Xing, Baolong
Genome-wide analysis of OSCA gene family members in Vigna radiata and their involvement in the osmotic response
title Genome-wide analysis of OSCA gene family members in Vigna radiata and their involvement in the osmotic response
title_full Genome-wide analysis of OSCA gene family members in Vigna radiata and their involvement in the osmotic response
title_fullStr Genome-wide analysis of OSCA gene family members in Vigna radiata and their involvement in the osmotic response
title_full_unstemmed Genome-wide analysis of OSCA gene family members in Vigna radiata and their involvement in the osmotic response
title_short Genome-wide analysis of OSCA gene family members in Vigna radiata and their involvement in the osmotic response
title_sort genome-wide analysis of osca gene family members in vigna radiata and their involvement in the osmotic response
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8422765/
https://www.ncbi.nlm.nih.gov/pubmed/34493199
http://dx.doi.org/10.1186/s12870-021-03184-2
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