Nucleosomes protect DNA from DNA methylation in vivo and in vitro

被引:50
|
作者
Felle, Max [1 ]
Hoffmeister, Helen [1 ]
Rothammer, Julia [1 ]
Fuchs, Andreas [1 ]
Exler, Josef H. [1 ]
Laengst, Gernot [1 ]
机构
[1] Univ Regensburg, Inst Biochem 3, D-93053 Regensburg, Germany
关键词
DE-NOVO METHYLATION; ENZYMATIC-PROPERTIES; CHROMATIN-STRUCTURE; GENOMIC DNA; DNMT3A; METHYLTRANSFERASES; MOUSE; LSH; MUTATIONS; MECHANISM;
D O I
10.1093/nar/gkr263
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
Positioned nucleosomes limit the access of proteins to DNA. However, the impact of nucleosomes on DNA methylation in vitro and in vivo is poorly understood. Here, we performed a detailed analysis of nucleosome binding and nucleosomal DNA methylation by the de novo methyltransferases. We show that compared to linker DNA, nucleosomal DNA is largely devoid of CpG methylation. ATP-dependent chromatin remodelling frees nucleosomal CpG dinucleotides and renders the remodelled nucleosome a 2-fold better substrate for Dnmt3a methyltransferase compared to free DNA. These results reflect the situation in vivo, as quantification of nucleosomal DNA methylation levels in HeLa cells shows a 2-fold decrease of nucleosomal DNA methylation levels compared to linker DNA. Our findings suggest that nucleosomal positions are stably maintained in vivo and nucleosomal occupancy is a major determinant of global DNA methylation patterns in vivo.
引用
收藏
页码:6956 / 6969
页数:14
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