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Evolutionary and genomic comparisons of hybrid uninucleate and nonhybrid Rhizoctonia fungi
The basidiomycetous fungal genus, Rhizoctonia, can cause severe damage to many plants and is composed of multinucleate, binucleate, and uninucleate species differing in pathogenicity. Here we generated chromosome-scale genome assemblies of the three nuclear types of Rhizoctonia isolates. The genomic...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7884421/ https://www.ncbi.nlm.nih.gov/pubmed/33589695 http://dx.doi.org/10.1038/s42003-021-01724-y |
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author | Li, Cheng Guo, Zejian Zhou, Shanyue Han, Qingyue Zhang, Manman Peng, Youliang Hsiang, Tom Chen, Xujun |
author_facet | Li, Cheng Guo, Zejian Zhou, Shanyue Han, Qingyue Zhang, Manman Peng, Youliang Hsiang, Tom Chen, Xujun |
author_sort | Li, Cheng |
collection | PubMed |
description | The basidiomycetous fungal genus, Rhizoctonia, can cause severe damage to many plants and is composed of multinucleate, binucleate, and uninucleate species differing in pathogenicity. Here we generated chromosome-scale genome assemblies of the three nuclear types of Rhizoctonia isolates. The genomic comparisons revealed that the uninucleate JN strain likely arose by somatic hybridization of two binucleate isolates, and maintained a diploid nucleus. Homeolog gene pairs in the JN genome have experienced both decelerated or accelerated evolution. Homeolog expression dominance occurred between JN subgenomes, in which differentially expressed genes show potentially less evolutionary constraint than the genes without. Analysis of mating-type genes suggested that Rhizoctonia maintains the ancestral tetrapolarity of the Basidiomycota. Long terminal repeat-retrotransposons displayed a reciprocal correlation with the chromosomal GC content in the three chromosome-scale genomes. The more aggressive multinucleate XN strain had more genes encoding enzymes for host cell wall decomposition. These findings demonstrate some evolutionary changes of a recently derived hybrid and in multiple nuclear types of Rhizoctonia. |
format | Online Article Text |
id | pubmed-7884421 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-78844212021-02-25 Evolutionary and genomic comparisons of hybrid uninucleate and nonhybrid Rhizoctonia fungi Li, Cheng Guo, Zejian Zhou, Shanyue Han, Qingyue Zhang, Manman Peng, Youliang Hsiang, Tom Chen, Xujun Commun Biol Article The basidiomycetous fungal genus, Rhizoctonia, can cause severe damage to many plants and is composed of multinucleate, binucleate, and uninucleate species differing in pathogenicity. Here we generated chromosome-scale genome assemblies of the three nuclear types of Rhizoctonia isolates. The genomic comparisons revealed that the uninucleate JN strain likely arose by somatic hybridization of two binucleate isolates, and maintained a diploid nucleus. Homeolog gene pairs in the JN genome have experienced both decelerated or accelerated evolution. Homeolog expression dominance occurred between JN subgenomes, in which differentially expressed genes show potentially less evolutionary constraint than the genes without. Analysis of mating-type genes suggested that Rhizoctonia maintains the ancestral tetrapolarity of the Basidiomycota. Long terminal repeat-retrotransposons displayed a reciprocal correlation with the chromosomal GC content in the three chromosome-scale genomes. The more aggressive multinucleate XN strain had more genes encoding enzymes for host cell wall decomposition. These findings demonstrate some evolutionary changes of a recently derived hybrid and in multiple nuclear types of Rhizoctonia. Nature Publishing Group UK 2021-02-15 /pmc/articles/PMC7884421/ /pubmed/33589695 http://dx.doi.org/10.1038/s42003-021-01724-y Text en © The Author(s) 2021 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Li, Cheng Guo, Zejian Zhou, Shanyue Han, Qingyue Zhang, Manman Peng, Youliang Hsiang, Tom Chen, Xujun Evolutionary and genomic comparisons of hybrid uninucleate and nonhybrid Rhizoctonia fungi |
title | Evolutionary and genomic comparisons of hybrid uninucleate and nonhybrid Rhizoctonia fungi |
title_full | Evolutionary and genomic comparisons of hybrid uninucleate and nonhybrid Rhizoctonia fungi |
title_fullStr | Evolutionary and genomic comparisons of hybrid uninucleate and nonhybrid Rhizoctonia fungi |
title_full_unstemmed | Evolutionary and genomic comparisons of hybrid uninucleate and nonhybrid Rhizoctonia fungi |
title_short | Evolutionary and genomic comparisons of hybrid uninucleate and nonhybrid Rhizoctonia fungi |
title_sort | evolutionary and genomic comparisons of hybrid uninucleate and nonhybrid rhizoctonia fungi |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7884421/ https://www.ncbi.nlm.nih.gov/pubmed/33589695 http://dx.doi.org/10.1038/s42003-021-01724-y |
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