Synthetic DNA fragments bearing ICR cis elements become differentially methylated and recapitulate genomic imprinting in transgenic mice
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Title
Synthetic DNA fragments bearing ICR cis elements become differentially methylated and recapitulate genomic imprinting in transgenic mice
Authors
Keywords
Genomic imprinting, DNA methylation, <em class=EmphasisTypeItalic >H19</em>, CTCF, Sox-Oct, ZFP57
Journal
Epigenetics & Chromatin
Volume 11, Issue 1, Pages -
Publisher
Springer Nature
Online
2018-06-29
DOI
10.1186/s13072-018-0207-z
References
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Related references
Note: Only part of the references are listed.- Maternal H3K27me3 controls DNA methylation-independent imprinting
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- De novoDNA methylation through the 5′-segment of theH19ICR maintains its imprint during early embryogenesis
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- Genomic imprinting in development, growth, behavior and stem cells
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- Sox-Oct motifs contribute to maintenance of the unmethylated H19 ICR in YAC transgenic mice
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- The Chicken HS4 Insulator Element Does Not Protect the H19 ICR from Differential DNA Methylation in Yeast Artificial Chromosome Transgenic Mouse
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- Contribution of Intragenic DNA Methylation in Mouse Gametic DNA Methylomes to Establish Oocyte-Specific Heritable Marks
- (2012) Hisato Kobayashi et al. PLoS Genetics
- Zinc Finger Protein ZFP57 Requires Its Co-factor to Recruit DNA Methyltransferases and Maintains DNA Methylation Imprint in Embryonic Stem Cells via Its Transcriptional Repression Domain
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- In Embryonic Stem Cells, ZFP57/KAP1 Recognize a Methylated Hexanucleotide to Affect Chromatin and DNA Methylation of Imprinting Control Regions
- (2011) Simon Quenneville et al. MOLECULAR CELL
- Dynamic CpG island methylation landscape in oocytes and preimplantation embryos
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- CTCF binding is not the epigenetic mark that establishes post-fertilization methylation imprinting in the transgenic H19 ICR
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