Intraindividual dynamics of transcriptome and genome-wide stability of DNA methylation

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作者
Ryohei Furukawa
Tsuyoshi Hachiya
Hideki Ohmomo
Yuh Shiwa
Kanako Ono
Sadafumi Suzuki
Mamoru Satoh
Jiro Hitomi
Kenji Sobue
Atsushi Shimizu
机构
[1] Iwate Tohoku Medical Megabank Organization,Division of Biomedical Information Analysis
[2] Iwate Medical University,Division of Biobank and Data Management
[3] 2-1-1 Nishitokuta,Department of Physiology
[4] Yahaba-cho,Division of Biomedical Information Analysis
[5] Shiwa-gun,Department of Anatomy
[6] Iwate Tohoku Medical Megabank Organization,Department of Neuroscience
[7] Iwate Medical University,undefined
[8] Keio University School of Medicine,undefined
[9] Community Medical Supports and Health Record Informatics,undefined
[10] Iwate Tohoku Medical Megabank Organization,undefined
[11] Iwate Medical University Disaster Reconstruction Center,undefined
[12] Institute for Biomedical Science,undefined
[13] Iwate Medical University,undefined
[14] Deputy Executive Director,undefined
[15] Iwate Tohoku Medical Megabank Organization,undefined
[16] Disaster Reconstruction Center,undefined
[17] Iwate Medical University,undefined
[18] School of Medicine,undefined
[19] Iwate Medical University,undefined
[20] Executive Director,undefined
[21] Iwate Tohoku Medical Megabank Organization,undefined
[22] Disaster Reconstruction Center,undefined
[23] Iwate Medical University,undefined
[24] Institute for Biomedical Science,undefined
[25] Iwate Medical University,undefined
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摘要
Cytosine methylation at CpG dinucleotides is an epigenetic mechanism that affects the gene expression profiles responsible for the functional differences in various cells and tissues. Although gene expression patterns are dynamically altered in response to various stimuli, the intraindividual dynamics of DNA methylation in human cells are yet to be fully understood. Here, we investigated the extent to which DNA methylation contributes to the dynamics of gene expression by collecting 24 blood samples from two individuals over a period of 3 months. Transcriptome and methylome association analyses revealed that only ~2% of dynamic changes in gene expression could be explained by the intraindividual variation of DNA methylation levels in peripheral blood mononuclear cells and purified monocytes. These results showed that DNA methylation levels remain stable for at least several months, suggesting that disease-associated DNA methylation markers are useful for estimating the risk of disease manifestation.
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