Identification and functional analysis of LecRLK genes in Taxodium ‘Zhongshanshan’

Background Lectin receptor-like protein kinases (LecRLKs) can transform external stimuli into intracellular signals and play important regulatory roles in plant development and response to environmental stressors. However, research on the LecRLK gene family of conifers has seldom been reported. Meth...

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Main Authors: Jinbo Guo, Hao Duan, Lei Xuan, Ziyang Wang, Jianfeng Hua, Chaoguang Yu, Yunlong Yin, Mingzhi Li, Ying Yang
Format: Article
Language:English
Published: PeerJ Inc. 2019-08-01
Series:PeerJ
Subjects:
Online Access:https://peerj.com/articles/7498.pdf
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author Jinbo Guo
Hao Duan
Lei Xuan
Ziyang Wang
Jianfeng Hua
Chaoguang Yu
Yunlong Yin
Mingzhi Li
Ying Yang
author_facet Jinbo Guo
Hao Duan
Lei Xuan
Ziyang Wang
Jianfeng Hua
Chaoguang Yu
Yunlong Yin
Mingzhi Li
Ying Yang
author_sort Jinbo Guo
collection DOAJ
description Background Lectin receptor-like protein kinases (LecRLKs) can transform external stimuli into intracellular signals and play important regulatory roles in plant development and response to environmental stressors. However, research on the LecRLK gene family of conifers has seldom been reported. Methods Putative LecRLK genes were identified in the transcriptome of Taxodium ‘Zhongshanshan’. The classification, domain structures, subcellular localization prediction, and expression patterns of LecRLK genes, as well as co-expressed genes, were analyzed using bioinformatics methods. Fifteen representative genes were further selected for qRT-PCR analysis in six tissues and under five different environmental stressor conditions. Results In total, 297 LecRLK genes were identified, including 155 G-type, 140 L-type, and 2 C-type. According to the classification, G-type and L-type LecRLK genes both can be organized into seven groups. The domain architecture of G-type proteins were more complex compared with that of L- and C-type proteins. Conservative motifs were found in G-type and L-type diverse lectin domains. Prediction and transient expression experiments to determine subcellular localization showed that LecRLKs were mainly concentrated in the cell membrane system, and some members were located at multiple sites at the same time. RNA-seq-based transcriptomics analysis suggested functional redundancy and divergence within each group. Unigenes co-expressed with LecRLKs in the transcriptome were found to be enriched in pathways related to signal transduction and environmental adaptation. Furthermore, qRT-PCR analysis of representative genes showed evidence of functional divergence between different groups. Conclusions This is the first study to conduct an identification and expression analysis of the LecRLK gene family in Taxodium. These results provide a basis for future studies on the evolution and function of this important gene family in Taxodium.
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spelling doaj.art-29e01bca9db54b2f90c210373150adf42023-12-03T09:18:54ZengPeerJ Inc.PeerJ2167-83592019-08-017e749810.7717/peerj.7498Identification and functional analysis of LecRLK genes in Taxodium ‘Zhongshanshan’Jinbo Guo0Hao Duan1Lei Xuan2Ziyang Wang3Jianfeng Hua4Chaoguang Yu5Yunlong Yin6Mingzhi Li7Ying Yang8Jiangsu Engineering Research Center for Taxodium Rich. Germplasm Innovation and Propagation, Institute of Botany, Jiangsu Province and Chinese Academy of Sciences (Nanjing Botanical Garden Mem. Sun Yat-Sen), Nanjing, ChinaJiangsu Engineering Research Center for Taxodium Rich. Germplasm Innovation and Propagation, Institute of Botany, Jiangsu Province and Chinese Academy of Sciences (Nanjing Botanical Garden Mem. Sun Yat-Sen), Nanjing, ChinaJiangsu Engineering Research Center for Taxodium Rich. Germplasm Innovation and Propagation, Institute of Botany, Jiangsu Province and Chinese Academy of Sciences (Nanjing Botanical Garden Mem. Sun Yat-Sen), Nanjing, ChinaJiangsu Engineering Research Center for Taxodium Rich. Germplasm Innovation and Propagation, Institute of Botany, Jiangsu Province and Chinese Academy of Sciences (Nanjing Botanical Garden Mem. Sun Yat-Sen), Nanjing, ChinaJiangsu Engineering Research Center for Taxodium Rich. Germplasm Innovation and Propagation, Institute of Botany, Jiangsu Province and Chinese Academy of Sciences (Nanjing Botanical Garden Mem. Sun Yat-Sen), Nanjing, ChinaJiangsu Engineering Research Center for Taxodium Rich. Germplasm Innovation and Propagation, Institute of Botany, Jiangsu Province and Chinese Academy of Sciences (Nanjing Botanical Garden Mem. Sun Yat-Sen), Nanjing, ChinaJiangsu Engineering Research Center for Taxodium Rich. Germplasm Innovation and Propagation, Institute of Botany, Jiangsu Province and Chinese Academy of Sciences (Nanjing Botanical Garden Mem. Sun Yat-Sen), Nanjing, ChinaGenepioneer Biotechnologies Co. Ltd, Nanjing, ChinaJiangsu Engineering Research Center for Taxodium Rich. Germplasm Innovation and Propagation, Institute of Botany, Jiangsu Province and Chinese Academy of Sciences (Nanjing Botanical Garden Mem. Sun Yat-Sen), Nanjing, ChinaBackground Lectin receptor-like protein kinases (LecRLKs) can transform external stimuli into intracellular signals and play important regulatory roles in plant development and response to environmental stressors. However, research on the LecRLK gene family of conifers has seldom been reported. Methods Putative LecRLK genes were identified in the transcriptome of Taxodium ‘Zhongshanshan’. The classification, domain structures, subcellular localization prediction, and expression patterns of LecRLK genes, as well as co-expressed genes, were analyzed using bioinformatics methods. Fifteen representative genes were further selected for qRT-PCR analysis in six tissues and under five different environmental stressor conditions. Results In total, 297 LecRLK genes were identified, including 155 G-type, 140 L-type, and 2 C-type. According to the classification, G-type and L-type LecRLK genes both can be organized into seven groups. The domain architecture of G-type proteins were more complex compared with that of L- and C-type proteins. Conservative motifs were found in G-type and L-type diverse lectin domains. Prediction and transient expression experiments to determine subcellular localization showed that LecRLKs were mainly concentrated in the cell membrane system, and some members were located at multiple sites at the same time. RNA-seq-based transcriptomics analysis suggested functional redundancy and divergence within each group. Unigenes co-expressed with LecRLKs in the transcriptome were found to be enriched in pathways related to signal transduction and environmental adaptation. Furthermore, qRT-PCR analysis of representative genes showed evidence of functional divergence between different groups. Conclusions This is the first study to conduct an identification and expression analysis of the LecRLK gene family in Taxodium. These results provide a basis for future studies on the evolution and function of this important gene family in Taxodium.https://peerj.com/articles/7498.pdf‘Zhongshanshan’Lectin receptor-like kinase (LecRLK)TaxodiumDomainarchitectureqRT-PCRExpression pattern
spellingShingle Jinbo Guo
Hao Duan
Lei Xuan
Ziyang Wang
Jianfeng Hua
Chaoguang Yu
Yunlong Yin
Mingzhi Li
Ying Yang
Identification and functional analysis of LecRLK genes in Taxodium ‘Zhongshanshan’
PeerJ
‘Zhongshanshan’
Lectin receptor-like kinase (LecRLK)
Taxodium
Domainarchitecture
qRT-PCR
Expression pattern
title Identification and functional analysis of LecRLK genes in Taxodium ‘Zhongshanshan’
title_full Identification and functional analysis of LecRLK genes in Taxodium ‘Zhongshanshan’
title_fullStr Identification and functional analysis of LecRLK genes in Taxodium ‘Zhongshanshan’
title_full_unstemmed Identification and functional analysis of LecRLK genes in Taxodium ‘Zhongshanshan’
title_short Identification and functional analysis of LecRLK genes in Taxodium ‘Zhongshanshan’
title_sort identification and functional analysis of lecrlk genes in taxodium zhongshanshan
topic ‘Zhongshanshan’
Lectin receptor-like kinase (LecRLK)
Taxodium
Domainarchitecture
qRT-PCR
Expression pattern
url https://peerj.com/articles/7498.pdf
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