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Phylogenomic and Evolutionary Analyses Reveal Diversifications of SET-Domain Proteins in Fungi
In recent years, many publications have established histone lysine methylation as a central epigenetic modification in the regulation of chromatin and transcription. The histone lysine methyltransferases contain a conserved SET domain and are widely distributed in various organisms. However, a compr...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9692433/ https://www.ncbi.nlm.nih.gov/pubmed/36354926 http://dx.doi.org/10.3390/jof8111159 |
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author | Ding, Guoqing Shang, Liqiu Zhou, Wenliang Lu, Siyi Zhou, Zong Huang, Xinyi Li, Juan |
author_facet | Ding, Guoqing Shang, Liqiu Zhou, Wenliang Lu, Siyi Zhou, Zong Huang, Xinyi Li, Juan |
author_sort | Ding, Guoqing |
collection | PubMed |
description | In recent years, many publications have established histone lysine methylation as a central epigenetic modification in the regulation of chromatin and transcription. The histone lysine methyltransferases contain a conserved SET domain and are widely distributed in various organisms. However, a comprehensive study on the origin and diversification of the SET-domain-containing genes in fungi has not been conducted. In this study, a total of 3816 SET-domain-containing genes, which were identified and characterized using HmmSearch from 229 whole genomes sequenced fungal species, were used to ascertain their evolution and diversification in fungi. Using the CLANS program, all the SET-domain-containing genes were grouped into three main clusters, and each cluster contains several groups. Domain organization analysis showed that genes belonging to the same group have similar sequence structures. In contrast, different groups process domain organizations or locations differently, suggesting the SET-domain-containing genes belonging to different groups may have obtained distinctive regulatory mechanisms during their evolution. These genes that conduct the histone methylations (such as H3K4me, H3K9me, H3K27me, H4K20me, H3K36me) are mainly grouped into Cluster 1 while the other genes grouped into Clusters 2 and 3 are still functionally undetermined. Our results also showed that numerous gene duplication and loss events have happened during the evolution of those fungal SET-domain-containing proteins. Our results provide novel insights into the roles of SET-domain genes in fungal evolution and pave a fundamental path to further understanding the epigenetic basis of gene regulation in fungi. |
format | Online Article Text |
id | pubmed-9692433 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-96924332022-11-26 Phylogenomic and Evolutionary Analyses Reveal Diversifications of SET-Domain Proteins in Fungi Ding, Guoqing Shang, Liqiu Zhou, Wenliang Lu, Siyi Zhou, Zong Huang, Xinyi Li, Juan J Fungi (Basel) Article In recent years, many publications have established histone lysine methylation as a central epigenetic modification in the regulation of chromatin and transcription. The histone lysine methyltransferases contain a conserved SET domain and are widely distributed in various organisms. However, a comprehensive study on the origin and diversification of the SET-domain-containing genes in fungi has not been conducted. In this study, a total of 3816 SET-domain-containing genes, which were identified and characterized using HmmSearch from 229 whole genomes sequenced fungal species, were used to ascertain their evolution and diversification in fungi. Using the CLANS program, all the SET-domain-containing genes were grouped into three main clusters, and each cluster contains several groups. Domain organization analysis showed that genes belonging to the same group have similar sequence structures. In contrast, different groups process domain organizations or locations differently, suggesting the SET-domain-containing genes belonging to different groups may have obtained distinctive regulatory mechanisms during their evolution. These genes that conduct the histone methylations (such as H3K4me, H3K9me, H3K27me, H4K20me, H3K36me) are mainly grouped into Cluster 1 while the other genes grouped into Clusters 2 and 3 are still functionally undetermined. Our results also showed that numerous gene duplication and loss events have happened during the evolution of those fungal SET-domain-containing proteins. Our results provide novel insights into the roles of SET-domain genes in fungal evolution and pave a fundamental path to further understanding the epigenetic basis of gene regulation in fungi. MDPI 2022-11-02 /pmc/articles/PMC9692433/ /pubmed/36354926 http://dx.doi.org/10.3390/jof8111159 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Ding, Guoqing Shang, Liqiu Zhou, Wenliang Lu, Siyi Zhou, Zong Huang, Xinyi Li, Juan Phylogenomic and Evolutionary Analyses Reveal Diversifications of SET-Domain Proteins in Fungi |
title | Phylogenomic and Evolutionary Analyses Reveal Diversifications of SET-Domain Proteins in Fungi |
title_full | Phylogenomic and Evolutionary Analyses Reveal Diversifications of SET-Domain Proteins in Fungi |
title_fullStr | Phylogenomic and Evolutionary Analyses Reveal Diversifications of SET-Domain Proteins in Fungi |
title_full_unstemmed | Phylogenomic and Evolutionary Analyses Reveal Diversifications of SET-Domain Proteins in Fungi |
title_short | Phylogenomic and Evolutionary Analyses Reveal Diversifications of SET-Domain Proteins in Fungi |
title_sort | phylogenomic and evolutionary analyses reveal diversifications of set-domain proteins in fungi |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9692433/ https://www.ncbi.nlm.nih.gov/pubmed/36354926 http://dx.doi.org/10.3390/jof8111159 |
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