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Phytophthora methylomes are modulated by 6mA methyltransferases and associated with adaptive genome regions

BACKGROUND: Filamentous plant pathogen genomes often display a bipartite architecture with gene-sparse, repeat-rich compartments serving as a cradle for adaptive evolution. The extent to which this two-speed genome architecture is associated with genome-wide DNA modifications is unknown. RESULTS: We...

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Autores principales: Chen, Han, Shu, Haidong, Wang, Liyuan, Zhang, Fan, Li, Xi, Ochola, Sylvans Ochieng, Mao, Fei, Ma, Hongyu, Ye, Wenwu, Gu, Tingting, Jiang, Lubin, Wu, Yufeng, Wang, Yuanchao, Kamoun, Sophien, Dong, Suomeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6211444/
https://www.ncbi.nlm.nih.gov/pubmed/30382931
http://dx.doi.org/10.1186/s13059-018-1564-4
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author Chen, Han
Shu, Haidong
Wang, Liyuan
Zhang, Fan
Li, Xi
Ochola, Sylvans Ochieng
Mao, Fei
Ma, Hongyu
Ye, Wenwu
Gu, Tingting
Jiang, Lubin
Wu, Yufeng
Wang, Yuanchao
Kamoun, Sophien
Dong, Suomeng
author_facet Chen, Han
Shu, Haidong
Wang, Liyuan
Zhang, Fan
Li, Xi
Ochola, Sylvans Ochieng
Mao, Fei
Ma, Hongyu
Ye, Wenwu
Gu, Tingting
Jiang, Lubin
Wu, Yufeng
Wang, Yuanchao
Kamoun, Sophien
Dong, Suomeng
author_sort Chen, Han
collection PubMed
description BACKGROUND: Filamentous plant pathogen genomes often display a bipartite architecture with gene-sparse, repeat-rich compartments serving as a cradle for adaptive evolution. The extent to which this two-speed genome architecture is associated with genome-wide DNA modifications is unknown. RESULTS: We show that the oomycetes Phytophthora infestans and Phytophthora sojae possess functional adenine N6-methylation (6mA) methyltransferases that modulate patterns of 6mA marks across the genome. In contrast, 5-methylcytosine could not be detected in these species. Methylated DNA IP sequencing (MeDIP-seq) of each species reveals 6mA is depleted around the transcription start sites (TSSs) and is associated with lowly expressed genes, particularly transposable elements. Genes occupying the gene-sparse regions have higher levels of 6mA in both genomes, possibly implicating the methylome in adaptive evolution. All six putative adenine methyltransferases from P. infestans and P. sojae, except PsDAMT2, display robust enzymatic activities. Surprisingly, single knockouts in P. sojae significantly reduce in vivo 6mA levels, indicating that the three enzymes are not fully redundant. MeDIP-seq of the psdamt3 mutant reveals uneven 6mA methylation reduction across genes, suggesting that PsDAMT3 may have a preference for gene body methylation after the TSS. Furthermore, transposable elements such as DNA elements are more active in the psdamt3 mutant. A large number of genes, particularly those from the adaptive genomic compartment, are differentially expressed. CONCLUSIONS: Our findings provide evidence that 6mA modification is potentially an epigenetic mark in Phytophthora genomes, and complex patterns of 6mA methylation may be associated with adaptive evolution in these important plant pathogens. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13059-018-1564-4) contains supplementary material, which is available to authorized users.
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spelling pubmed-62114442018-11-08 Phytophthora methylomes are modulated by 6mA methyltransferases and associated with adaptive genome regions Chen, Han Shu, Haidong Wang, Liyuan Zhang, Fan Li, Xi Ochola, Sylvans Ochieng Mao, Fei Ma, Hongyu Ye, Wenwu Gu, Tingting Jiang, Lubin Wu, Yufeng Wang, Yuanchao Kamoun, Sophien Dong, Suomeng Genome Biol Research BACKGROUND: Filamentous plant pathogen genomes often display a bipartite architecture with gene-sparse, repeat-rich compartments serving as a cradle for adaptive evolution. The extent to which this two-speed genome architecture is associated with genome-wide DNA modifications is unknown. RESULTS: We show that the oomycetes Phytophthora infestans and Phytophthora sojae possess functional adenine N6-methylation (6mA) methyltransferases that modulate patterns of 6mA marks across the genome. In contrast, 5-methylcytosine could not be detected in these species. Methylated DNA IP sequencing (MeDIP-seq) of each species reveals 6mA is depleted around the transcription start sites (TSSs) and is associated with lowly expressed genes, particularly transposable elements. Genes occupying the gene-sparse regions have higher levels of 6mA in both genomes, possibly implicating the methylome in adaptive evolution. All six putative adenine methyltransferases from P. infestans and P. sojae, except PsDAMT2, display robust enzymatic activities. Surprisingly, single knockouts in P. sojae significantly reduce in vivo 6mA levels, indicating that the three enzymes are not fully redundant. MeDIP-seq of the psdamt3 mutant reveals uneven 6mA methylation reduction across genes, suggesting that PsDAMT3 may have a preference for gene body methylation after the TSS. Furthermore, transposable elements such as DNA elements are more active in the psdamt3 mutant. A large number of genes, particularly those from the adaptive genomic compartment, are differentially expressed. CONCLUSIONS: Our findings provide evidence that 6mA modification is potentially an epigenetic mark in Phytophthora genomes, and complex patterns of 6mA methylation may be associated with adaptive evolution in these important plant pathogens. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13059-018-1564-4) contains supplementary material, which is available to authorized users. BioMed Central 2018-10-31 /pmc/articles/PMC6211444/ /pubmed/30382931 http://dx.doi.org/10.1186/s13059-018-1564-4 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Chen, Han
Shu, Haidong
Wang, Liyuan
Zhang, Fan
Li, Xi
Ochola, Sylvans Ochieng
Mao, Fei
Ma, Hongyu
Ye, Wenwu
Gu, Tingting
Jiang, Lubin
Wu, Yufeng
Wang, Yuanchao
Kamoun, Sophien
Dong, Suomeng
Phytophthora methylomes are modulated by 6mA methyltransferases and associated with adaptive genome regions
title Phytophthora methylomes are modulated by 6mA methyltransferases and associated with adaptive genome regions
title_full Phytophthora methylomes are modulated by 6mA methyltransferases and associated with adaptive genome regions
title_fullStr Phytophthora methylomes are modulated by 6mA methyltransferases and associated with adaptive genome regions
title_full_unstemmed Phytophthora methylomes are modulated by 6mA methyltransferases and associated with adaptive genome regions
title_short Phytophthora methylomes are modulated by 6mA methyltransferases and associated with adaptive genome regions
title_sort phytophthora methylomes are modulated by 6ma methyltransferases and associated with adaptive genome regions
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6211444/
https://www.ncbi.nlm.nih.gov/pubmed/30382931
http://dx.doi.org/10.1186/s13059-018-1564-4
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