Non-coding RNA directed DNA demethylation of Sphk1 CpG island

被引:123
作者
Imamura, T [1 ]
Yamamoto, S [1 ]
Ohgane, J [1 ]
Hattori, N [1 ]
Tanaka, S [1 ]
Shiota, K [1 ]
机构
[1] Univ Tokyo, Lab Cellular Biochem, Bunkyo Ku, Tokyo 1138657, Japan
基金
日本学术振兴会;
关键词
DNA methylation; demethylation; antisense RNA; non-coding; CpG island; sphingosine kinase; tissue-specific;
D O I
10.1016/j.bbrc.2004.07.159
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
The formation of DNA methylation patterns is one of the epigenetic events that underlie mammalian development. The Sphk1 CpG island is a target for tissue-dependent DNA methylation as well as a template for generating multiple subtypes. The number of mammalian non-coding RNA genes is rapidly expanding. In this study, we found endogenous antisense transcripts, Khps1 subtypes with different sizes (600-20,000 nt). A subtype, Khps1a, was a 1290-bp, non-coding, 5'-capped and 3'-polyadenylated RNA that originated from the CpG island and overlapped with a tissue-dependent differentially methylated region (T-DMR) of Sphk1. Intriguingly, overexpression of two fragments of Khps1 caused demethylation of CG sites in the T-DMR. Furthermore, this RNA-directed demethylation was associated with DNA methylation at three CC(A/T)GG sites in the T-DMR. The link between the RNA-directed CG demethylation and non-CG methylation provides a novel mechanism of epigenetic regulation and potential tool for epigenetic manipulation of mammalian cells. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:593 / 600
页数:8
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