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DNA methylation landscape of 16 canine somatic tissues by methylation-sensitive restriction enzyme-based next generation sequencing

DNA methylation plays important functions in gene expression regulation that is involved in individual development and various diseases. DNA methylation has been well studied in human and model organisms, but only limited data exist in companion animals like dog. Using methylation-sensitive restrict...

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Autores principales: Yamazaki, Jumpei, Matsumoto, Yuki, Jelinek, Jaroslav, Ishizaki, Teita, Maeda, Shingo, Watanabe, Kei, Ishihara, Genki, Yamagishi, Junya, Takiguchi, Mitsuyoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8113467/
https://www.ncbi.nlm.nih.gov/pubmed/33976289
http://dx.doi.org/10.1038/s41598-021-89279-0
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author Yamazaki, Jumpei
Matsumoto, Yuki
Jelinek, Jaroslav
Ishizaki, Teita
Maeda, Shingo
Watanabe, Kei
Ishihara, Genki
Yamagishi, Junya
Takiguchi, Mitsuyoshi
author_facet Yamazaki, Jumpei
Matsumoto, Yuki
Jelinek, Jaroslav
Ishizaki, Teita
Maeda, Shingo
Watanabe, Kei
Ishihara, Genki
Yamagishi, Junya
Takiguchi, Mitsuyoshi
author_sort Yamazaki, Jumpei
collection PubMed
description DNA methylation plays important functions in gene expression regulation that is involved in individual development and various diseases. DNA methylation has been well studied in human and model organisms, but only limited data exist in companion animals like dog. Using methylation-sensitive restriction enzyme-based next generation sequencing (Canine DREAM), we obtained canine DNA methylation maps of 16 somatic tissues from two dogs. In total, we evaluated 130,861 CpG sites. The majority of CpG sites were either highly methylated (> 70%, 52.5–64.6% of all CpG sites analyzed) or unmethylated (< 30%, 22.5–28.0% of all CpG sites analyzed) which are methylation patterns similar to other species. The overall methylation status of CpG sites across the 32 methylomes were remarkably similar. However, the tissue types were clearly defined by principle component analysis and hierarchical clustering analysis with DNA methylome. We found 6416 CpG sites located closely at promoter region of genes and inverse correlation between DNA methylation and gene expression of these genes. Our study provides basic dataset for DNA methylation profiles in dogs.
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spelling pubmed-81134672021-05-12 DNA methylation landscape of 16 canine somatic tissues by methylation-sensitive restriction enzyme-based next generation sequencing Yamazaki, Jumpei Matsumoto, Yuki Jelinek, Jaroslav Ishizaki, Teita Maeda, Shingo Watanabe, Kei Ishihara, Genki Yamagishi, Junya Takiguchi, Mitsuyoshi Sci Rep Article DNA methylation plays important functions in gene expression regulation that is involved in individual development and various diseases. DNA methylation has been well studied in human and model organisms, but only limited data exist in companion animals like dog. Using methylation-sensitive restriction enzyme-based next generation sequencing (Canine DREAM), we obtained canine DNA methylation maps of 16 somatic tissues from two dogs. In total, we evaluated 130,861 CpG sites. The majority of CpG sites were either highly methylated (> 70%, 52.5–64.6% of all CpG sites analyzed) or unmethylated (< 30%, 22.5–28.0% of all CpG sites analyzed) which are methylation patterns similar to other species. The overall methylation status of CpG sites across the 32 methylomes were remarkably similar. However, the tissue types were clearly defined by principle component analysis and hierarchical clustering analysis with DNA methylome. We found 6416 CpG sites located closely at promoter region of genes and inverse correlation between DNA methylation and gene expression of these genes. Our study provides basic dataset for DNA methylation profiles in dogs. Nature Publishing Group UK 2021-05-11 /pmc/articles/PMC8113467/ /pubmed/33976289 http://dx.doi.org/10.1038/s41598-021-89279-0 Text en © The Author(s) 2021 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/) .
spellingShingle Article
Yamazaki, Jumpei
Matsumoto, Yuki
Jelinek, Jaroslav
Ishizaki, Teita
Maeda, Shingo
Watanabe, Kei
Ishihara, Genki
Yamagishi, Junya
Takiguchi, Mitsuyoshi
DNA methylation landscape of 16 canine somatic tissues by methylation-sensitive restriction enzyme-based next generation sequencing
title DNA methylation landscape of 16 canine somatic tissues by methylation-sensitive restriction enzyme-based next generation sequencing
title_full DNA methylation landscape of 16 canine somatic tissues by methylation-sensitive restriction enzyme-based next generation sequencing
title_fullStr DNA methylation landscape of 16 canine somatic tissues by methylation-sensitive restriction enzyme-based next generation sequencing
title_full_unstemmed DNA methylation landscape of 16 canine somatic tissues by methylation-sensitive restriction enzyme-based next generation sequencing
title_short DNA methylation landscape of 16 canine somatic tissues by methylation-sensitive restriction enzyme-based next generation sequencing
title_sort dna methylation landscape of 16 canine somatic tissues by methylation-sensitive restriction enzyme-based next generation sequencing
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8113467/
https://www.ncbi.nlm.nih.gov/pubmed/33976289
http://dx.doi.org/10.1038/s41598-021-89279-0
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