Dynamic link of DNA demethylation, DNA strand breaks and repair in mouse zygotes

被引:183
作者
Wossidlo, Mark [1 ]
Arand, Julia [1 ]
Sebastiano, Vittorio [2 ]
Lepikhov, Konstantin [1 ]
Boiani, Michele [2 ]
Reinhardt, Richard [3 ]
Schoeler, Hans [2 ]
Walter, Joern [1 ]
机构
[1] Univ Saarland, Dept Genet Epigenet, D-66123 Saarbrucken, Germany
[2] Max Planck Inst Mol Biomed, Munster, Germany
[3] Max Planck Inst Mol Genet, Berlin, Germany
关键词
gamma H2A.X; DNA demethylation; DNA repair; epigenetic reprogramming; mouse zygote; HISTONE H2AX PHOSPHORYLATION; POLYMERASE-ALPHA; TRANSCRIPTIONAL ACTIVITY; PATERNAL GENOME; MAMMALIAN DNA; METHYLATION; REPLICATION; GLYCOSYLASE; COMPLEX; 5-HYDROXYMETHYLCYTOSINE;
D O I
10.1038/emboj.2010.80
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In mammalian zygotes, the 5-methyl-cytosine (5mC) content of paternal chromosomes is rapidly changed by a yet unknown but presumably active enzymatic mechanism. Here, we describe the developmental dynamics and parental asymmetries of DNA methylation in relation to the presence of DNA strand breaks, DNA repair markers and a precise timing of zygotic DNA replication. The analysis shows that distinct pre-replicative (active) and replicative (active and passive) phases of DNA demethylation can be observed. These phases of DNA demethylation are concomitant with the appearance of DNA strand breaks and DNA repair markers such as gamma H2A.X and PARP-1, respectively. The same correlations are found in cloned embryos obtained after somatic cell nuclear transfer. Together, the data suggest that (1) DNA-methylation reprogramming is more complex and extended as anticipated earlier and (2) the DNA demethylation, particularly the rapid loss of 5mC in paternal DNA, is likely to be linked to DNA repair mechanisms. The EMBO Journal (2010) 29, 1877-1888. doi:10.1038/emboj.2010.80; Published online 4 May 2010
引用
收藏
页码:1877 / 1888
页数:12
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