Abstract
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.
Original language | English |
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Pages (from-to) | 593-600 |
Number of pages | 8 |
Journal | Biochemical and Biophysical Research Communications |
Volume | 322 |
Issue number | 2 |
DOIs | |
Publication status | Published - 2004 Sept 17 |
Externally published | Yes |
Keywords
- Antisense RNA
- CpG island
- Demethylation
- DNA methylation
- Non-coding
- Sphingosine kinase
- Tissue-specific
ASJC Scopus subject areas
- Biochemistry
- Biophysics
- Molecular Biology