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• W4225647527 startingPage "5080" @default.
• W4225647527 abstract "The Dlk1-Dio3 imprinted domain is controlled by an imprinting control region (ICR) called IG-DMR that is hypomethylated on the maternal allele and hypermethylated on the paternal allele. Although several genetic mutation experiments have shown that IG-DMR is essential for imprinting control of the domain, how DNA methylation itself functions has not been elucidated. Here, we performed both gain and loss of DNA methylation experiments targeting IG-DMR by transiently introducing CRISPR/Cas9 based-targeted DNA methylation editing tools along with one guide RNA into mouse ES cells. Altered DNA methylation, particularly at IG-DMR-Rep, which is a tandem repeat containing ZFP57 methylated DNA-binding protein binding motifs, affected the imprinting state of the whole domain, including DNA methylation, imprinted gene expression, and histone modifications. Moreover, the altered imprinting states were persistent through neuronal differentiation. Our results suggest that the DNA methylation state at IG-DMR-Rep, but not other sites in IG-DMR, is a master element to determine whether the allele behaves as the intrinsic maternal or paternal allele. Meanwhile, this study provides a robust strategy and methodology to study core DNA methylation in cis-regulatory elements, such as ICRs and enhancers." @default.
• W4225647527 created "2022-05-05" @default.
• W4225647527 creator A5052962043 @default.
• W4225647527 date "2022-05-11" @default.
• W4225647527 modified "2023-10-02" @default.
• W4225647527 title "Epigenome editing reveals core DNA methylation for imprinting control in the <i>Dlk1-Dio3</i> imprinted domain" @default.
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• W4225647527 doi "https://doi.org/10.1093/nar/gkac344" @default.
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