Epigenetic mechanisms in mammals

被引:352
作者
Kim, J. K. [1 ]
Samaranayake, M. [1 ]
Pradhan, S. [1 ]
机构
[1] New England Biolabs Inc, Ipswich, MA 01938 USA
关键词
DNA methylation; histone modification; chromatin; methylation spreading; silencing; EMBRYONIC STEM-CELLS; HISTONE LYSINE METHYLATION; POLYCOMB GROUP PROTEINS; NOVO DNA METHYLATION; X-INACTIVATION; DE-NOVO; GENE-EXPRESSION; CPG-ISLANDS; CYTOSINE METHYLATION; DEVELOPMENTAL REGULATORS;
D O I
10.1007/s00018-008-8432-4
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
DNA and histone methylation are linked and subjected to mitotic inheritance in mammals. Yet how methylation is propagated and maintained between successive cell divisions is not fully understood. A series of enzyme families that can add methylation marks to cytosine nucleobases, and lysine and arginine amino acid residues has been discovered. Apart from methyltransferases, there are also histone modification enzymes and accessory proteins, which can facilitate and/or target epigenetic marks. Several lysine and arginine demethylases have been discovered recently, and the presence of an active DNA demethylase is speculated in mammalian cells. A mammalian methyl DNA binding protein MBD2 and de novo DNA methyltransferase DNMT3A and DNMT3B are shown experimentally to possess DNA demethylase activity. Thus, complex mammalian epigenetic mechanisms appear to be dynamic yet reversible along with a well-choreographed set of events that take place during mammalian development.
引用
收藏
页码:596 / 612
页数:17
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