Histone H4 Lysine 20 methylation: key player in epigenetic regulation of genomic integrity

被引:306
作者
Jorgensen, Stine [1 ]
Schotta, Gunnar [2 ]
Sorensen, Claus Storgaard [1 ]
机构
[1] Univ Copenhagen, BRIC, DK-2200 Copenhagen N, Denmark
[2] Univ Munich, Adolf Butenandt Inst, Munich Ctr Integrated Prot Sci CiPSM, D-80336 Munich, Germany
基金
英国医学研究理事会;
关键词
DNA-DAMAGE; CELL-CYCLE; METHYLTRANSFERASE SET8; TUMOR SUPPRESSION; PROTEIN; 53BP1; S-PHASE; CHROMATIN; PR-SET7; REPLICATION; CHECKPOINT;
D O I
10.1093/nar/gkt012
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Maintenance of genomic integrity is essential to ensure normal organismal development and to prevent diseases such as cancer. Nuclear DNA is packaged into chromatin, and thus genome maintenance can be influenced by distinct chromatin environments. In particular, post-translational modifications of histones have emerged as key regulators of genomic integrity. Intense research during the past few years has revealed histone H4 lysine 20 methylation (H4K20me) as critically important for the biological processes that ensure genome integrity, such as DNA damage repair, DNA replication and chromatin compaction. The distinct H4K20 methylation states are mediated by SET8/PR-Set7 that catalyses monomethylation of H4K20, whereas SUV4-20H1 and SUV4-20H2 enzymes mediate further H4K20 methylation to H4K20me2 and H4K20me3. Disruption of these H4K20-specific histone methyltransferases leads to genomic instability, demonstrating the important functions of H4K20 methylation in genome maintenance. In this review, we explain molecular mechanisms underlying these defects and discuss novel ideas for furthering our understanding of genome maintenance in higher eukaryotes.
引用
收藏
页码:2797 / 2806
页数:10
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