The orphan nuclear receptor GCNF recruits DNA methyltransferase for Oct-314 silencing

被引:66
作者
Sato, N
Kondo, M
Arai, K
机构
[1] Tokyo Metropolitan Inst Med Sci, Cytokine Project, Bunkyo Ku, Tokyo 1138613, Japan
[2] Univ Tokyo, LSBM, RCAST, Tokyo 1538904, Japan
基金
日本学术振兴会;
关键词
Oct-314; DNA methylation; DNA methyltransferase; silencing; Dnmt3;
D O I
10.1016/j.bbrc.2006.04.007
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
Somatic DNA inethylation patterns are determined in part by the de novo methylation that occurs after early embryonic demethylation. Oct-314, a pluripotency gene. is unmethylated in the blastocyst. but undergoes de novo methylation and silencing during gastrulation. Here we show that the transcriptional repressor GCNF recruits DNA methyltransferase to the Oct-314 promoter and facilitates its methylation. Although acetylation of historic H3 at lysine 9 (K9) and/or 14 (K14) and inethylation of H3 at lysine 4 (K4) decrease during this period. Lis do Oct-314 transcript levels, H3K9 and H3K27 methylation levels remain constant, indicating that DNA methylation does not require repressive histone modifications. We found that GCNF interacts directly with Dnmt3 molecule(s) and verified that this interaction induces the methylation of the Oct-314 promoter. Our finding suggests a model in which differentiation-induced GCNF recruits de novo DNA methyltransferase and facilitates the silencing of a pluripotency gene. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:845 / 851
页数:7
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