Dlk1 and Gtl2 are reciprocally imprinted genes located 80 kb apart on mouse chromosome 12. Similarities between this domain and that of the well characterized Igf2-H19 locus have been previously noted. Comparative genomic and epigenetic analysis of these two domains might help identify allele-specific epigenetic regulatory elements and common features involved in aspects of imprinting control. Here we describe a detailed methylation analysis of the Dlk1-Gtl2 domain on both parental alleles in the mouse. Like the Igf2- H79 domain, areas of differential methylation are hypermethylated on the paternal allele and hypomethylated on the maternal allele. Three differentially methylated regions (DMRs), each with different epigenetic characteristics...
AbstractThe mouse delta-like homolog 1 and type III iodothyronine deiodinase (Dlk1–Dio3) imprinted d...
Genomic imprinting is a conserved epigenetic phenomenon in eutherian mammals, with regards both to t...
Genomic imprinting is an epigenetic phenomenon that results in unequal expression of homologous mate...
AbstractThe distal portion of mouse chromosome 12 is imprinted. To date, however, Gtl2 is the only i...
The Dlk1-Gtl2 domain on mouse chromosome 12 contains reciprocally imprinted genes with the potential...
AbstractDlk1 and Gtl2 are reciprocally expressed imprinted genes located on mouse chromosome 12. The...
Abstract Background The Dlk1 and Gtl2 genes define a region of mouse chromosome 12 that is subject t...
The mouse Igft and H19 genes lie 70-kb apart on chromosome 7 and are reciprocally imprinted. Two reg...
Imprinted genes and their control elements occur in clusters in the mammalian genome and carry epige...
Imprinted genes and their control elements occur in clusters in the mammalian genome and carry epige...
Imprinted genes and their control elements occur in clusters in the mammalian genome and carry epige...
The imprinted Igf2 gene is active only on the paternal allele in most tissues. Its imprinting involv...
Genomic imprinting causes parental origin-specific gene expression. Cis-acting regulatory elements t...
Abstract Background Differential DNA methylation plays a critical role in the regulation of imprinte...
In different eukaryotic model systems, chromatin and gene expression are modulated by post-translati...
AbstractThe mouse delta-like homolog 1 and type III iodothyronine deiodinase (Dlk1–Dio3) imprinted d...
Genomic imprinting is a conserved epigenetic phenomenon in eutherian mammals, with regards both to t...
Genomic imprinting is an epigenetic phenomenon that results in unequal expression of homologous mate...
AbstractThe distal portion of mouse chromosome 12 is imprinted. To date, however, Gtl2 is the only i...
The Dlk1-Gtl2 domain on mouse chromosome 12 contains reciprocally imprinted genes with the potential...
AbstractDlk1 and Gtl2 are reciprocally expressed imprinted genes located on mouse chromosome 12. The...
Abstract Background The Dlk1 and Gtl2 genes define a region of mouse chromosome 12 that is subject t...
The mouse Igft and H19 genes lie 70-kb apart on chromosome 7 and are reciprocally imprinted. Two reg...
Imprinted genes and their control elements occur in clusters in the mammalian genome and carry epige...
Imprinted genes and their control elements occur in clusters in the mammalian genome and carry epige...
Imprinted genes and their control elements occur in clusters in the mammalian genome and carry epige...
The imprinted Igf2 gene is active only on the paternal allele in most tissues. Its imprinting involv...
Genomic imprinting causes parental origin-specific gene expression. Cis-acting regulatory elements t...
Abstract Background Differential DNA methylation plays a critical role in the regulation of imprinte...
In different eukaryotic model systems, chromatin and gene expression are modulated by post-translati...
AbstractThe mouse delta-like homolog 1 and type III iodothyronine deiodinase (Dlk1–Dio3) imprinted d...
Genomic imprinting is a conserved epigenetic phenomenon in eutherian mammals, with regards both to t...
Genomic imprinting is an epigenetic phenomenon that results in unequal expression of homologous mate...