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Comprehensive identification and expression analyses of the SnRK gene family in Casuarina equisetifolia in response to salt stress

BACKGROUND: Sucrose nonfermenting-1 (SNF1)-related protein kinases (SnRKs) play crucial roles in plant signaling pathways and stress adaptive responses by activating protein phosphorylation pathways. However, there have been no comprehensive studies of the SnRK gene family in the widely planted salt...

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Autores principales: Ai, Di, Wang, Yujiao, Wei, Yongcheng, Zhang, Jie, Meng, Jingxiang, Zhang, Yong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9733041/
https://www.ncbi.nlm.nih.gov/pubmed/36482301
http://dx.doi.org/10.1186/s12870-022-03961-7
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author Ai, Di
Wang, Yujiao
Wei, Yongcheng
Zhang, Jie
Meng, Jingxiang
Zhang, Yong
author_facet Ai, Di
Wang, Yujiao
Wei, Yongcheng
Zhang, Jie
Meng, Jingxiang
Zhang, Yong
author_sort Ai, Di
collection PubMed
description BACKGROUND: Sucrose nonfermenting-1 (SNF1)-related protein kinases (SnRKs) play crucial roles in plant signaling pathways and stress adaptive responses by activating protein phosphorylation pathways. However, there have been no comprehensive studies of the SnRK gene family in the widely planted salt-tolerant tree species Casuarina equisetifolia. Here, we comprehensively analyze this gene family in C. equisetifolia using genome-wide identification, characterization, and profiling of expression changes in response to salt stress. RESULTS: A total of 26 CeqSnRK genes were identified, which were divided into three subfamilies (SnRK1, SnRK2, and SnRK3). The intron–exon structures and protein‑motif compositions were similar within each subgroup but differed among groups. Ka/Ks ratio analysis indicated that the CeqSnRK family has undergone purifying selection, and cis-regulatory element analysis suggested that these genes may be involved in plant development and responses to various environmental stresses. A heat map was generated using quantitative real‑time PCR (RT-qPCR) data from 26 CeqSnRK genes, suggesting that they were expressed in different tissues. We also examined the expression of all CeqSnRK genes under exposure to different salt concentrations using RT-qPCR, finding that most CeqSnRK genes were regulated by different salt treatments. Moreover, co-expression network analysis revealed synergistic effects among CeqSnRK genes. CONCLUSIONS: Several CeqSnRK genes (CeqSnRK3.7, CeqSnRK3.16, CeqSnRK3.17) were up-regulated following salt treatment. Among them, CeqSnRK3.16 expression was significantly up-regulated under various salt treatments, identifying this as a candidate gene salt stress tolerance gene. In addition, CeqSnRK3.16 showed significant expression change correlations with multiple genes under salt stress, indicating that it might exhibit synergistic effects with other genes in response to salt stress. This comprehensive analysis will provide a theoretical reference for CeqSnRK gene functional verification and the role of these genes in salt tolerance. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12870-022-03961-7.
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spelling pubmed-97330412022-12-10 Comprehensive identification and expression analyses of the SnRK gene family in Casuarina equisetifolia in response to salt stress Ai, Di Wang, Yujiao Wei, Yongcheng Zhang, Jie Meng, Jingxiang Zhang, Yong BMC Plant Biol Research Article BACKGROUND: Sucrose nonfermenting-1 (SNF1)-related protein kinases (SnRKs) play crucial roles in plant signaling pathways and stress adaptive responses by activating protein phosphorylation pathways. However, there have been no comprehensive studies of the SnRK gene family in the widely planted salt-tolerant tree species Casuarina equisetifolia. Here, we comprehensively analyze this gene family in C. equisetifolia using genome-wide identification, characterization, and profiling of expression changes in response to salt stress. RESULTS: A total of 26 CeqSnRK genes were identified, which were divided into three subfamilies (SnRK1, SnRK2, and SnRK3). The intron–exon structures and protein‑motif compositions were similar within each subgroup but differed among groups. Ka/Ks ratio analysis indicated that the CeqSnRK family has undergone purifying selection, and cis-regulatory element analysis suggested that these genes may be involved in plant development and responses to various environmental stresses. A heat map was generated using quantitative real‑time PCR (RT-qPCR) data from 26 CeqSnRK genes, suggesting that they were expressed in different tissues. We also examined the expression of all CeqSnRK genes under exposure to different salt concentrations using RT-qPCR, finding that most CeqSnRK genes were regulated by different salt treatments. Moreover, co-expression network analysis revealed synergistic effects among CeqSnRK genes. CONCLUSIONS: Several CeqSnRK genes (CeqSnRK3.7, CeqSnRK3.16, CeqSnRK3.17) were up-regulated following salt treatment. Among them, CeqSnRK3.16 expression was significantly up-regulated under various salt treatments, identifying this as a candidate gene salt stress tolerance gene. In addition, CeqSnRK3.16 showed significant expression change correlations with multiple genes under salt stress, indicating that it might exhibit synergistic effects with other genes in response to salt stress. This comprehensive analysis will provide a theoretical reference for CeqSnRK gene functional verification and the role of these genes in salt tolerance. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12870-022-03961-7. BioMed Central 2022-12-09 /pmc/articles/PMC9733041/ /pubmed/36482301 http://dx.doi.org/10.1186/s12870-022-03961-7 Text en © The Author(s) 2022 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
Ai, Di
Wang, Yujiao
Wei, Yongcheng
Zhang, Jie
Meng, Jingxiang
Zhang, Yong
Comprehensive identification and expression analyses of the SnRK gene family in Casuarina equisetifolia in response to salt stress
title Comprehensive identification and expression analyses of the SnRK gene family in Casuarina equisetifolia in response to salt stress
title_full Comprehensive identification and expression analyses of the SnRK gene family in Casuarina equisetifolia in response to salt stress
title_fullStr Comprehensive identification and expression analyses of the SnRK gene family in Casuarina equisetifolia in response to salt stress
title_full_unstemmed Comprehensive identification and expression analyses of the SnRK gene family in Casuarina equisetifolia in response to salt stress
title_short Comprehensive identification and expression analyses of the SnRK gene family in Casuarina equisetifolia in response to salt stress
title_sort comprehensive identification and expression analyses of the snrk gene family in casuarina equisetifolia in response to salt stress
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9733041/
https://www.ncbi.nlm.nih.gov/pubmed/36482301
http://dx.doi.org/10.1186/s12870-022-03961-7
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