The DOI matches its Crossref record; 59 of the 59 references it cites were found in a registry or an index.
Contribution of Intragenic DNA Methylation in Mouse Gametic DNA Methylomes to Establish Oocyte-Specific Heritable Marks
Open accessAbstract
Genome-wide dynamic changes in DNA methylation are indispensable for germline development and genomic imprinting in mammals. Here, we report single-base resolution DNA methylome and transcriptome maps of mouse germ cells, generated using whole-genome shotgun bisulfite sequencing and cDNA sequencing (mRNA-seq). Oocyte genomes showed a significant positive correlation between mRNA transcript levels and methylation of the transcribed region. Sperm genomes had nearly complete coverage of methylation, except in the CpG-rich regions, and showed a significant negative correlation between gene expression and promoter methylation. Thus, these methylome maps revealed that oocytes and sperms are widely different in the extent and distribution of DNA methylation. Furthermore, a comparison of oocyte and sperm methylomes identified more than 1,600 CpG islands differentially methylated in oocytes and sperm (germline differentially methylated regions, gDMRs), in addition to the known imprinting control regions (ICRs). About half of these differentially methylated DNA sequences appear to be at least partially resistant to the global DNA demethylation that occurs during preimplantation development. In the absence of Dnmt3L, neither methylation of most oocyte-methylated gDMRs nor intragenic methylation was observed. There was also genome-wide hypomethylation, and partial methylation at particular retrotransposons, while maintaining global gene expression, in oocytes. Along with the identification of the many Dnmt3L-dependent gDMRs at intragenic regions, the present results suggest that oocyte methylation can be divided into 2 types: Dnmt3L-dependent methylation, which is required for maternal methylation imprinting, and Dnmt3L-independent methylation, which might be essential for endogenous retroviral DNA silencing. The present data provide entirely new perspectives on the evaluation of epigenetic markers in germline cells.
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Cites
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Human DNA methylomes at base resolution show widespread epigenomic differences
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Shotgun bisulphite sequencing of the Arabidopsis genome reveals DNA methylation patterning
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DNA methylation: roles in mammalian development
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“5), the genome of inner cell mass (ICM) cells becomes hypomethylated ( 21% CpG methylation) as compared to sperm (90%) or oocyte (40%) methylome after replication-dependent dilution of maternal 5mC and paternal 5hmC/5fC/5caC (Kobayashi et al., 2012).”
InfluentialThe Dynamics of Genome-wide DNA Methylation Reprogramming in Mouse Primordial Germ Cells
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Vitamin C induces Tet-dependent DNA demethylation and a blastocyst-like state in ES cells
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DNA methylation dynamics during epigenetic reprogramming in the germline and preimplantation embryos
Messerschmidt, D. M., Knowles, B. B., & Solter, D. (2014) · Genes & Development · doi:10.1101/gad.234294.113 · Cited by 729
Metadata
- Authors
- Kobayashi, H., Sakurai, T., Imai, M., Takahashi, N., Fukuda, A., Yayoi, O., Sato, S., Nakabayashi, K., Hata, K., Sotomaru, Y., Suzuki, Y., & Kono, T.
- Venue
- PLoS Genetics
- Publisher
- Public Library of Science (PLoS)
- Published
- 2012-01-05
- Volume
- 8
- Issue
- 1
- Pages
- e1002440
- ISSN
- 1553-7390 (ISSN-L)
- 1553-7404
- OpenAlex
- W2034219651
- Cited by
- 535
- References
- 59
- FWCI
- 19.75
- Type
- journal article
- Language
- en
- Open access
- gold
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- Kobayashi, H., Sakurai, T., Imai, M., Takahashi, N., Fukuda, A., Yayoi, O., Sato, S., Nakabayashi, K., Hata, K., Sotomaru, Y., Suzuki, Y., & Kono, T. (2012). Contribution of Intragenic DNA Methylation in Mouse Gametic DNA Methylomes to Establish Oocyte-Specific Heritable Marks. PLoS Genetics. https://doi.org/10.1371/journal.pgen.1002440
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