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The DNMT3A PWWP domain is essential for the normal DNA methylation landscape in mouse somatic cells and oocytes

DNA methylation at CG sites is important for gene regulation and embryonic development. In mouse oocytes, de novo CG methylation requires preceding transcription-coupled histone mark H3K36me3 and is mediated by a DNA methyltransferase DNMT3A. DNMT3A has a PWWP domain, which recognizes H3K36me2/3, an...

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Autores principales: Kibe, Kanako, Shirane, Kenjiro, Ohishi, Hiroaki, Uemura, Shuhei, Toh, Hidehiro, Sasaki, Hiroyuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8162659/
https://www.ncbi.nlm.nih.gov/pubmed/34048432
http://dx.doi.org/10.1371/journal.pgen.1009570
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author Kibe, Kanako
Shirane, Kenjiro
Ohishi, Hiroaki
Uemura, Shuhei
Toh, Hidehiro
Sasaki, Hiroyuki
author_facet Kibe, Kanako
Shirane, Kenjiro
Ohishi, Hiroaki
Uemura, Shuhei
Toh, Hidehiro
Sasaki, Hiroyuki
author_sort Kibe, Kanako
collection PubMed
description DNA methylation at CG sites is important for gene regulation and embryonic development. In mouse oocytes, de novo CG methylation requires preceding transcription-coupled histone mark H3K36me3 and is mediated by a DNA methyltransferase DNMT3A. DNMT3A has a PWWP domain, which recognizes H3K36me2/3, and heterozygous mutations in this domain, including D329A substitution, cause aberrant CG hypermethylation of regions marked by H3K27me3 in somatic cells, leading to a dwarfism phenotype. We herein demonstrate that D329A homozygous mice show greater CG hypermethylation and severer dwarfism. In oocytes, D329A substitution did not affect CG methylation of H3K36me2/3-marked regions, including maternally methylated imprinting control regions; rather, it caused aberrant hypermethylation in regions lacking H3K36me2/3, including H3K27me3-marked regions. Thus, the role of the PWWP domain in CG methylation seems similar in somatic cells and oocytes; however, there were cell-type-specific differences in affected regions. The major satellite repeat was also hypermethylated in mutant oocytes. Contrary to the CA hypomethylation in somatic cells, the mutation caused hypermethylation at CH sites, including CA sites. Surprisingly, oocytes expressing only the mutated protein could support embryonic and postnatal development. Our study reveals that the DNMT3A PWWP domain is important for suppressing aberrant CG hypermethylation in both somatic cells and oocytes but that D329A mutation has little impact on the developmental potential of oocytes.
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spelling pubmed-81626592021-06-10 The DNMT3A PWWP domain is essential for the normal DNA methylation landscape in mouse somatic cells and oocytes Kibe, Kanako Shirane, Kenjiro Ohishi, Hiroaki Uemura, Shuhei Toh, Hidehiro Sasaki, Hiroyuki PLoS Genet Research Article DNA methylation at CG sites is important for gene regulation and embryonic development. In mouse oocytes, de novo CG methylation requires preceding transcription-coupled histone mark H3K36me3 and is mediated by a DNA methyltransferase DNMT3A. DNMT3A has a PWWP domain, which recognizes H3K36me2/3, and heterozygous mutations in this domain, including D329A substitution, cause aberrant CG hypermethylation of regions marked by H3K27me3 in somatic cells, leading to a dwarfism phenotype. We herein demonstrate that D329A homozygous mice show greater CG hypermethylation and severer dwarfism. In oocytes, D329A substitution did not affect CG methylation of H3K36me2/3-marked regions, including maternally methylated imprinting control regions; rather, it caused aberrant hypermethylation in regions lacking H3K36me2/3, including H3K27me3-marked regions. Thus, the role of the PWWP domain in CG methylation seems similar in somatic cells and oocytes; however, there were cell-type-specific differences in affected regions. The major satellite repeat was also hypermethylated in mutant oocytes. Contrary to the CA hypomethylation in somatic cells, the mutation caused hypermethylation at CH sites, including CA sites. Surprisingly, oocytes expressing only the mutated protein could support embryonic and postnatal development. Our study reveals that the DNMT3A PWWP domain is important for suppressing aberrant CG hypermethylation in both somatic cells and oocytes but that D329A mutation has little impact on the developmental potential of oocytes. Public Library of Science 2021-05-28 /pmc/articles/PMC8162659/ /pubmed/34048432 http://dx.doi.org/10.1371/journal.pgen.1009570 Text en © 2021 Kibe et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Kibe, Kanako
Shirane, Kenjiro
Ohishi, Hiroaki
Uemura, Shuhei
Toh, Hidehiro
Sasaki, Hiroyuki
The DNMT3A PWWP domain is essential for the normal DNA methylation landscape in mouse somatic cells and oocytes
title The DNMT3A PWWP domain is essential for the normal DNA methylation landscape in mouse somatic cells and oocytes
title_full The DNMT3A PWWP domain is essential for the normal DNA methylation landscape in mouse somatic cells and oocytes
title_fullStr The DNMT3A PWWP domain is essential for the normal DNA methylation landscape in mouse somatic cells and oocytes
title_full_unstemmed The DNMT3A PWWP domain is essential for the normal DNA methylation landscape in mouse somatic cells and oocytes
title_short The DNMT3A PWWP domain is essential for the normal DNA methylation landscape in mouse somatic cells and oocytes
title_sort dnmt3a pwwp domain is essential for the normal dna methylation landscape in mouse somatic cells and oocytes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8162659/
https://www.ncbi.nlm.nih.gov/pubmed/34048432
http://dx.doi.org/10.1371/journal.pgen.1009570
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