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The impacts of allopolyploidization on Methyl-CpG-Binding Domain (MBD) gene family in Brassica napus

BACKGROUND: Polyploidization promotes species formation and is widespread in angiosperms. Genome changes dramatically bring opportunities and challenges to plants after polyploidy. Methyl-CpG-Binding Domain (MBD) proteins can recognize and bind to methylation sites and they play an important role in...

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Autores principales: Xiao, Yafang, Li, Mengdi, Wang, Jianbo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8900393/
https://www.ncbi.nlm.nih.gov/pubmed/35255818
http://dx.doi.org/10.1186/s12870-022-03485-0
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author Xiao, Yafang
Li, Mengdi
Wang, Jianbo
author_facet Xiao, Yafang
Li, Mengdi
Wang, Jianbo
author_sort Xiao, Yafang
collection PubMed
description BACKGROUND: Polyploidization promotes species formation and is widespread in angiosperms. Genome changes dramatically bring opportunities and challenges to plants after polyploidy. Methyl-CpG-Binding Domain (MBD) proteins can recognize and bind to methylation sites and they play an important role in the physiological process related to methylation in animals and plants. However, research on the influence of the allopolyploidization process on the MBD gene family is still lacking, so it is necessary to conduct a comprehensive analysis. RESULTS: In this study, twenty-two, ten and eleven MBD genes were identified in the genome of allotetraploid B. napus and its diploid ancestors, B. rapa and B. oleracea, respectively. Based on the clades of the MBD gene in Arabidopsis, rice and maize, we divided the new phylogenetic tree into 8 clades. Among them, the true MBD genes in Brassica existed in only 5 clades. Clade IV and Clade VI were unique in term of MBD genes in dicotyledons. Ka/Ks calculations showed that MBD genes underwent purifying selection in Brassica and may retain genes through sequence or functional differentiation early in evolution. In the process of allopolyploidization, the number of MBD gene introns increased, and the protein motifs changed. The MBD proteins had their own special motifs in each clade, and the MBD domains were only conserved in their clades. At the same time, the MBD genes were expressed in flower, leaf, silique, and stem tissues, and the expression levels of the different genes were significantly different, while the tissue specificity was not obvious. The allopolyploidization process may increase the number of cis-acting elements and activate the transposable elements. During allopolyploidization, the expression pattern of the MBD gene changes, which may be regulated by cis-acting elements and transposable elements. The number imbalance of cis-acting elements and transposable elements in A(n) and C(n) subgenomes may also lead to biased A(n) subgenome expression of the MBD gene in B. napus. CONCLUSIONS: In this study, by evaluating the number, structure, phylogeny and expression of the MBD gene in B. napus and its diploid ancestors, we increased the understanding of MBD genes in allopolyploids and provided a reference for future analysis of allopolyploidization. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12870-022-03485-0.
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spelling pubmed-89003932022-03-17 The impacts of allopolyploidization on Methyl-CpG-Binding Domain (MBD) gene family in Brassica napus Xiao, Yafang Li, Mengdi Wang, Jianbo BMC Plant Biol Research BACKGROUND: Polyploidization promotes species formation and is widespread in angiosperms. Genome changes dramatically bring opportunities and challenges to plants after polyploidy. Methyl-CpG-Binding Domain (MBD) proteins can recognize and bind to methylation sites and they play an important role in the physiological process related to methylation in animals and plants. However, research on the influence of the allopolyploidization process on the MBD gene family is still lacking, so it is necessary to conduct a comprehensive analysis. RESULTS: In this study, twenty-two, ten and eleven MBD genes were identified in the genome of allotetraploid B. napus and its diploid ancestors, B. rapa and B. oleracea, respectively. Based on the clades of the MBD gene in Arabidopsis, rice and maize, we divided the new phylogenetic tree into 8 clades. Among them, the true MBD genes in Brassica existed in only 5 clades. Clade IV and Clade VI were unique in term of MBD genes in dicotyledons. Ka/Ks calculations showed that MBD genes underwent purifying selection in Brassica and may retain genes through sequence or functional differentiation early in evolution. In the process of allopolyploidization, the number of MBD gene introns increased, and the protein motifs changed. The MBD proteins had their own special motifs in each clade, and the MBD domains were only conserved in their clades. At the same time, the MBD genes were expressed in flower, leaf, silique, and stem tissues, and the expression levels of the different genes were significantly different, while the tissue specificity was not obvious. The allopolyploidization process may increase the number of cis-acting elements and activate the transposable elements. During allopolyploidization, the expression pattern of the MBD gene changes, which may be regulated by cis-acting elements and transposable elements. The number imbalance of cis-acting elements and transposable elements in A(n) and C(n) subgenomes may also lead to biased A(n) subgenome expression of the MBD gene in B. napus. CONCLUSIONS: In this study, by evaluating the number, structure, phylogeny and expression of the MBD gene in B. napus and its diploid ancestors, we increased the understanding of MBD genes in allopolyploids and provided a reference for future analysis of allopolyploidization. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12870-022-03485-0. BioMed Central 2022-03-07 /pmc/articles/PMC8900393/ /pubmed/35255818 http://dx.doi.org/10.1186/s12870-022-03485-0 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
Xiao, Yafang
Li, Mengdi
Wang, Jianbo
The impacts of allopolyploidization on Methyl-CpG-Binding Domain (MBD) gene family in Brassica napus
title The impacts of allopolyploidization on Methyl-CpG-Binding Domain (MBD) gene family in Brassica napus
title_full The impacts of allopolyploidization on Methyl-CpG-Binding Domain (MBD) gene family in Brassica napus
title_fullStr The impacts of allopolyploidization on Methyl-CpG-Binding Domain (MBD) gene family in Brassica napus
title_full_unstemmed The impacts of allopolyploidization on Methyl-CpG-Binding Domain (MBD) gene family in Brassica napus
title_short The impacts of allopolyploidization on Methyl-CpG-Binding Domain (MBD) gene family in Brassica napus
title_sort impacts of allopolyploidization on methyl-cpg-binding domain (mbd) gene family in brassica napus
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8900393/
https://www.ncbi.nlm.nih.gov/pubmed/35255818
http://dx.doi.org/10.1186/s12870-022-03485-0
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