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DNA methylation on C5-Cytosine and N6-Adenine in the Bursaphelenchus xylophilus genome

BACKGROUND: The pinewood nematode is the causal agent of the pine wilt disease, which causes severe ecological and economic losses in coniferous forests. The invasion of pine wood nematode has undergone various rapid adaptations to a wide range of temperatures and to new hosts and vector insects. DN...

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Autores principales: Liu, Zhenkai, Li, Yongxia, Zhang, Xingyao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10631105/
https://www.ncbi.nlm.nih.gov/pubmed/37936063
http://dx.doi.org/10.1186/s12864-023-09783-7
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author Liu, Zhenkai
Li, Yongxia
Zhang, Xingyao
author_facet Liu, Zhenkai
Li, Yongxia
Zhang, Xingyao
author_sort Liu, Zhenkai
collection PubMed
description BACKGROUND: The pinewood nematode is the causal agent of the pine wilt disease, which causes severe ecological and economic losses in coniferous forests. The invasion of pine wood nematode has undergone various rapid adaptations to a wide range of temperatures and to new hosts and vector insects. DNA methylation may play crucial roles in the rapid adaptation of PWN during invasion. However, whether the PWN genome contins functional DNA modifications remains elusive. RESULTS: Here, we detected the extensive presence of 5-methylcytosine (5mC) and N6-methyladenine (6mA) in the B. xylophilus genome, with low methylation levels at most positions. Cytosines were methylated in the CpG, CHG. and CHH sequence contexts, with the lowest methylation levels at CpG sites. The methylation levels of CpG and 6mA in gene regions showed opposite trends. The changes in the abundance of 5mC and 6mA showed the same trends in response to temperature change, but opposite trends during development. Sequence and phylogenetic analyses showed that the proteins BxDAMT and BxNMAD have typical characteristics of a methylase and demethylase, respectively, and are conserved among species. CONCLUSIONS: These findings shed light on the epigenetic modifications present in the genome of PWN, and will improve our understanding of its invasiveness and evolution. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-023-09783-7.
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spelling pubmed-106311052023-11-07 DNA methylation on C5-Cytosine and N6-Adenine in the Bursaphelenchus xylophilus genome Liu, Zhenkai Li, Yongxia Zhang, Xingyao BMC Genomics Research BACKGROUND: The pinewood nematode is the causal agent of the pine wilt disease, which causes severe ecological and economic losses in coniferous forests. The invasion of pine wood nematode has undergone various rapid adaptations to a wide range of temperatures and to new hosts and vector insects. DNA methylation may play crucial roles in the rapid adaptation of PWN during invasion. However, whether the PWN genome contins functional DNA modifications remains elusive. RESULTS: Here, we detected the extensive presence of 5-methylcytosine (5mC) and N6-methyladenine (6mA) in the B. xylophilus genome, with low methylation levels at most positions. Cytosines were methylated in the CpG, CHG. and CHH sequence contexts, with the lowest methylation levels at CpG sites. The methylation levels of CpG and 6mA in gene regions showed opposite trends. The changes in the abundance of 5mC and 6mA showed the same trends in response to temperature change, but opposite trends during development. Sequence and phylogenetic analyses showed that the proteins BxDAMT and BxNMAD have typical characteristics of a methylase and demethylase, respectively, and are conserved among species. CONCLUSIONS: These findings shed light on the epigenetic modifications present in the genome of PWN, and will improve our understanding of its invasiveness and evolution. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-023-09783-7. BioMed Central 2023-11-07 /pmc/articles/PMC10631105/ /pubmed/37936063 http://dx.doi.org/10.1186/s12864-023-09783-7 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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 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
Liu, Zhenkai
Li, Yongxia
Zhang, Xingyao
DNA methylation on C5-Cytosine and N6-Adenine in the Bursaphelenchus xylophilus genome
title DNA methylation on C5-Cytosine and N6-Adenine in the Bursaphelenchus xylophilus genome
title_full DNA methylation on C5-Cytosine and N6-Adenine in the Bursaphelenchus xylophilus genome
title_fullStr DNA methylation on C5-Cytosine and N6-Adenine in the Bursaphelenchus xylophilus genome
title_full_unstemmed DNA methylation on C5-Cytosine and N6-Adenine in the Bursaphelenchus xylophilus genome
title_short DNA methylation on C5-Cytosine and N6-Adenine in the Bursaphelenchus xylophilus genome
title_sort dna methylation on c5-cytosine and n6-adenine in the bursaphelenchus xylophilus genome
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10631105/
https://www.ncbi.nlm.nih.gov/pubmed/37936063
http://dx.doi.org/10.1186/s12864-023-09783-7
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