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Loss of imprinting at the Dlk1-Gtl2 locus caused by insertional mutagenesis in the Gtl2 5' region.

Ekaterina Y Steshina | Michael S Carr | Elena A Glick | Aleksey Yevtodiyenko | Oliver K Appelbe | Jennifer V Schmidt
BMC genetics | 2006

The Dlk1 and Gtl2 genes define a region of mouse chromosome 12 that is subject to genomic imprinting, the parental allele-specific expression of a gene. Although imprinted genes play important roles in growth and development, the mechanisms by which imprinting is established and maintained are poorly understood. Differentially methylated regions (DMRs), which carry methylation on only one parental allele, are involved in imprinting control at many loci. The Dlk1-Gtl2 region contains three known DMRs, the Dlk1 DMR in the 3' region of Dlk1, the intergenic DMR 15 kb upstream of Gtl2, and the Gtl2 DMR at the Gtl2 promoter. Three mouse models are analyzed here that provide new information about the regulation of Dlk1-Gtl2 imprinting.

Pubmed ID: 17014736

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Associated grants

  • Agency: NICHD NIH HHS, United States
    Id: R01 HD042013
  • Agency: NICHD NIH HHS, United States
    Id: HD042013

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129S2(B6)-Meg3Gt(pGTi)216Gos/H (tool)

RRID:IMSR_EM:06878

Mus musculus with name 129S2(B6)-Meg3Gt(pGTi)216Gos/H from IMSR.

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BALB/cAnNCrl (tool)

RRID:MGI:2683685

laboratory mouse with name BALB/cAnNCrl from MGI.

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