摘要
组蛋白赖氨酸的甲基化在表观遗传调控中起着关键作用。组蛋白H3的K4、K9、K27、K36、K79和H4的K20均可被甲基化。组蛋白H3第9位赖氨酸的甲基化与基因的失活相关连;组蛋白H3第4位赖氨酸和第36位赖氨酸的甲基化与基因的激活相关连;组蛋白H3第27位赖氨酸的甲基化与同源盒基因沉默、X染色体失活、基因印记等基因沉默现象有关;组蛋白H3第79位赖氨酸的甲基化与防止基因失活和DNA修复有关。与此同时,组蛋白的去甲基化也受到更为广泛的关注。
Histone lysine methylation plays a key role in epigenetic regulation.There are five lysines within histone H3(K4, K9, K2.7, K36, K79). Besides, one lysine within histone H4(K2.0) has been shown to be methylated by specific histone lysine methyltransferase. Methylation at H3-K9 is associated with transcriptional repression, while methylation at H3-K4 andH3-K36 is associated with transcriptional activation. The methylation of histone H3-K2.7 was proved to be linked to several silencing phenomena including homeotic-gene silencing, X inactivation and genomic imprinting. H3-K79 methylation plays a role in DNA repair and transcriptional activation, and the extent and biological significance of histone demethylation will surely attract great attention.
出处
《遗传》
CAS
CSCD
北大核心
2007年第4期387-392,共6页
Hereditas(Beijing)
基金
国家自然科学基金项目(编号:30370334)资助~~