The DNMT3 Family of Mammalian De Novo DNA Methyltransferases

被引:124
作者
Chedin, Frederic [1 ]
机构
[1] Univ Calif Davis, Dept Mol & Cellular Biol, Davis, CA 95616 USA
来源
MODIFICATIONS OF NUCLEAR DNA AND ITS REGULATORY PROTEINS | 2011年 / 101卷
关键词
EMBRYONIC STEM-CELLS; GENOMIC METHYLATION PATTERNS; ENZYMATIC-PROPERTIES; PWWP DOMAIN; HISTONE H3; CYTOSINE METHYLTRANSFERASE; IMMUNODEFICIENCY SYNDROME; INITIAL-CHARACTERIZATION; EPIGENETIC MODIFICATIONS; CATALYTIC MECHANISM;
D O I
10.1016/B978-0-12-387685-0.00007-X
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
The deposition of DNA methylation at promoters of transposons, X-linked genes, imprinted genes, and other lineage-specific genes is clearly associated with long-term transcriptional silencing. Thus, DNA methylation represents a key layer of epigenetic information in mammals that is required for embryonic development, germline differentiation, and, as shown more recently, for the function and maturation of neuronal tissues. The DNMT3A, DNMT3B, and DNMT3L proteins are primarily responsible for the establishment of genomic DNA methylation patterns and, as such, play an important role in human developmental, reproductive, and mental health. Progress in our understanding of this important protein family has been rapid in recent years and has been accompanied by stunning developments in the analysis of the human DNA methylome in multiple cell types. This review focuses on recent developments in the characterization of the DNMT3 family of DNA methyltransferases at the biochemical, structural, and functional levels. Interconnections between the DNA-based and histone-based layers of epigenetic information are particularly highlighted, as it is now clear that de now methylation occurs chiefly in the context of nucleosomal templates.
引用
收藏
页码:255 / 285
页数:31
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