DNA methylation and the formation of heterochromatin in Neurospora crassa

被引:73
作者
Rountree, M. R. [1 ]
Selker, E. U. [1 ]
机构
[1] Univ Oregon, Inst Mol Biol, Eugene, OR 97403 USA
关键词
heterochromatin; DNA methylation; histone methylation; RIP; Neurospora; INDUCED POINT MUTATION; HISTONE H3 LYSINE-9; JMJC DOMAIN PROTEIN; EPIGENETIC CONTROL; RNA INTERFERENCE; CYTOSINE METHYLATION; CHROMATIN-STRUCTURE; MBD1; INTERACTS; HP1; MAINTENANCE;
D O I
10.1038/hdy.2010.44
中图分类号
Q14 [生态学(生物生态学)];
学科分类号
071012 ; 0713 ;
摘要
Studies of the control and function of DNA methylation in Neurospora crassa have led to a greater understanding of heterochromatin formation. DNA methylation in Neurospora is dependent on trimethylation of histone H3 lysine 9 (H3K9me3) by the histone methyltransferase, DIM-5. The linkage between these two methyl marks is facilitated by heterochromatin protein 1 (HP1), which serves as an adapter protein. HP1 binds to the H3K9me3 and recruits the DNA methyltransferase, DIM-2. Although HP1 links H3K9me3 to DNA methylation, it also serves to recruit the DNA methylation modifier complex to the edges of heterochromatin regions, where it serves to limit the spreading of the heterochromatin by countering H3K9me3. Heredity (2010) 105, 38-44; doi:10.1038/hdy.2010.44; published online 21 April 2010
引用
收藏
页码:38 / 44
页数:7
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