Imprinted silencing of Slc22a2 and Slc22a3 does not need transcriptional overlap between Igf2r and Air

被引:72
作者
Sleutels, F
Tjon, G
Ludwig, T
Barlow, DP [1 ]
机构
[1] OAW, Inst Mol Biol, Vienna, Austria
[2] Netherlands Canc Inst, Dept Mol Genet, Amsterdam, Netherlands
[3] Columbia Univ, Dept Anat & Cell Biol, New York, NY 10032 USA
关键词
genomic imprinting; Igf2r; non-coding RNA; Slc22a2; Slc22a3;
D O I
10.1093/emboj/cdg341
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
Silencing of the paternal allele of three imprinted genes (Igf2r, Slc22a2 and Slc22a3) requires cis expression of the Air RNA that overlaps the promoter of one of them (Igf2r). Air is a non-coding RNA whose mode of action is unknown. We tested the role of the Igf2r promoter and the role of transcriptional overlap between Igf2r and Air in silencing in this cluster. We analyzed imprinted expression in mice in which the Igf2r promoter is replaced by a thymidine kinase promoter that preserves a transcription overlap with Air, and in mice with a deleted Igf2r promoter that lack any transcriptional overlap with Air. Imprinted silencing of Air, Slc22a2 and Slc22a3 is maintained by the replacement promoter and also in the absence of transcriptional overlap with Air. These results exclude a role for the Igf2r promoter and for transcriptional overlap between Igf2r and Air in silencing Air, Slc22a2 and Slc22a3. Although these results do not completely exclude a role for a double-stranded RNA silencing mechanism, they do allow the possibility that the Air RNA has intrinsic cis silencing properties.
引用
收藏
页码:3696 / 3704
页数:9
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