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Elongation of the Kcnq1ot1 Transcript is Required for Genomic Imprinting of Neighboring Genes

Overview
Journal Genes Dev
Specialty Molecular Biology
Date 2006 May 17
PMID 16702402
Citations 222
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Abstract

The imprinted gene cluster at the telomeric end of mouse chromosome 7 contains a differentially methylated CpG island, KvDMR, that is required for the imprinting of multiple genes, including the genes encoding the maternally expressed placental-specific transcription factor ASCL2, the cyclin-dependent kinase CDKN1C, and the potassium channel KCNQ1. The KvDMR, which maps within intron 10 of Kcnq1, contains the promoter for a paternally expressed, noncoding, antisense transcript, Kcnq1ot1. A 244-base-pair deletion of the promoter on the paternal allele leads to the derepression of all silent genes tested. To distinguish between the loss of silencing as the consequence of the absence of transcription or the transcript itself, we prematurely truncated the Kcnq1ot1 transcript by inserting a transcriptional stop signal downstream of the promoter. We show that the lack of a full-length Kcnq1ot1 transcript on the paternal chromosome leads to the expression of genes that are normally paternally repressed. Finally, we demonstrate that five highly conserved repeats residing at the 5' end of the Kcnq1ot1 transcript are not required for imprinting at this locus.

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References
1.
Kanduri C, Pant V, Loukinov D, Pugacheva E, Qi C, Wolffe A . Functional association of CTCF with the insulator upstream of the H19 gene is parent of origin-specific and methylation-sensitive. Curr Biol. 2000; 10(14):853-6. DOI: 10.1016/s0960-9822(00)00597-2. View

2.
Fitzpatrick G, Soloway P, Higgins M . Regional loss of imprinting and growth deficiency in mice with a targeted deletion of KvDMR1. Nat Genet. 2002; 32(3):426-31. DOI: 10.1038/ng988. View

3.
Schoenherr C, Levorse J, Tilghman S . CTCF maintains differential methylation at the Igf2/H19 locus. Nat Genet. 2002; 33(1):66-9. DOI: 10.1038/ng1057. View

4.
Lin S, Youngson N, Takada S, Seitz H, Reik W, Paulsen M . Asymmetric regulation of imprinting on the maternal and paternal chromosomes at the Dlk1-Gtl2 imprinted cluster on mouse chromosome 12. Nat Genet. 2003; 35(1):97-102. DOI: 10.1038/ng1233. View

5.
Caspary T, Cleary M, Baker C, Guan X, Tilghman S . Multiple mechanisms regulate imprinting of the mouse distal chromosome 7 gene cluster. Mol Cell Biol. 1998; 18(6):3466-74. PMC: 108927. DOI: 10.1128/MCB.18.6.3466. View