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Gradual transition from mosaic to global DNA methylation patterns during deuterostome evolution
BACKGROUND: DNA methylation by the Dnmt family occurs in vertebrates and invertebrates, including ascidians, and is thought to play important roles in gene regulation and genome stability, especially in vertebrates. However, the global methylation patterns of vertebrates and invertebrates are distin...
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2957685/ https://www.ncbi.nlm.nih.gov/pubmed/21106124 http://dx.doi.org/10.1186/1471-2105-11-S7-S2 |
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author | Okamura, Kohji Matsumoto, Kazuaki A Nakai, Kenta |
author_facet | Okamura, Kohji Matsumoto, Kazuaki A Nakai, Kenta |
author_sort | Okamura, Kohji |
collection | PubMed |
description | BACKGROUND: DNA methylation by the Dnmt family occurs in vertebrates and invertebrates, including ascidians, and is thought to play important roles in gene regulation and genome stability, especially in vertebrates. However, the global methylation patterns of vertebrates and invertebrates are distinctive. Whereas almost all CpG sites are methylated in vertebrates, with the exception of those in CpG islands, the ascidian genome contains approximately equal amounts of methylated and unmethylated regions. Curiously, methylation status can be reliably estimated from the local frequency of CpG dinucleotides in the ascidian genome. Methylated and unmethylated regions tend to have few and many CpG sites, respectively, consistent with our knowledge of the methylation status of CpG islands and other regions in mammals. However, DNA methylation patterns and levels in vertebrates and invertebrates have not been analyzed in the same way. RESULTS: Using a new computational methodology based on the decomposition of the bimodal distributions of methylated and unmethylated regions, we estimated the extent of the global methylation patterns in a wide range of animals. We then examined the epigenetic changes in silico along the phylogenetic tree. We observed a gradual transition from fractional to global patterns of methylation in deuterostomes, rather than a clear demarcation between vertebrates and invertebrates. When we applied this methodology to six piscine genomes, some of which showed features similar to those of invertebrates. CONCLUSIONS: The mammalian global DNA methylation pattern was probably not acquired at an early stage of vertebrate evolution, but gradually expanded from that of a more ancient organism. |
format | Text |
id | pubmed-2957685 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-29576852010-10-21 Gradual transition from mosaic to global DNA methylation patterns during deuterostome evolution Okamura, Kohji Matsumoto, Kazuaki A Nakai, Kenta BMC Bioinformatics Proceedings BACKGROUND: DNA methylation by the Dnmt family occurs in vertebrates and invertebrates, including ascidians, and is thought to play important roles in gene regulation and genome stability, especially in vertebrates. However, the global methylation patterns of vertebrates and invertebrates are distinctive. Whereas almost all CpG sites are methylated in vertebrates, with the exception of those in CpG islands, the ascidian genome contains approximately equal amounts of methylated and unmethylated regions. Curiously, methylation status can be reliably estimated from the local frequency of CpG dinucleotides in the ascidian genome. Methylated and unmethylated regions tend to have few and many CpG sites, respectively, consistent with our knowledge of the methylation status of CpG islands and other regions in mammals. However, DNA methylation patterns and levels in vertebrates and invertebrates have not been analyzed in the same way. RESULTS: Using a new computational methodology based on the decomposition of the bimodal distributions of methylated and unmethylated regions, we estimated the extent of the global methylation patterns in a wide range of animals. We then examined the epigenetic changes in silico along the phylogenetic tree. We observed a gradual transition from fractional to global patterns of methylation in deuterostomes, rather than a clear demarcation between vertebrates and invertebrates. When we applied this methodology to six piscine genomes, some of which showed features similar to those of invertebrates. CONCLUSIONS: The mammalian global DNA methylation pattern was probably not acquired at an early stage of vertebrate evolution, but gradually expanded from that of a more ancient organism. BioMed Central 2010-10-15 /pmc/articles/PMC2957685/ /pubmed/21106124 http://dx.doi.org/10.1186/1471-2105-11-S7-S2 Text en Copyright ©2010 Okamura et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Proceedings Okamura, Kohji Matsumoto, Kazuaki A Nakai, Kenta Gradual transition from mosaic to global DNA methylation patterns during deuterostome evolution |
title | Gradual transition from mosaic to global DNA methylation patterns during deuterostome evolution |
title_full | Gradual transition from mosaic to global DNA methylation patterns during deuterostome evolution |
title_fullStr | Gradual transition from mosaic to global DNA methylation patterns during deuterostome evolution |
title_full_unstemmed | Gradual transition from mosaic to global DNA methylation patterns during deuterostome evolution |
title_short | Gradual transition from mosaic to global DNA methylation patterns during deuterostome evolution |
title_sort | gradual transition from mosaic to global dna methylation patterns during deuterostome evolution |
topic | Proceedings |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2957685/ https://www.ncbi.nlm.nih.gov/pubmed/21106124 http://dx.doi.org/10.1186/1471-2105-11-S7-S2 |
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