Characterization of the C3 YAC Contig from Proximal Mouse Chromosome 17 and Analysis of Allelic Expression of Genes Flanking the Imprinted Igf2r Gene
pmid: 9268631
Characterization of the C3 YAC Contig from Proximal Mouse Chromosome 17 and Analysis of Allelic Expression of Genes Flanking the Imprinted Igf2r Gene
The imprinted mouse insulin-like growth factor type 2 receptor (Igf2r) maps to the middle of a gene-rich region in band A2 of mouse chromosome 17. The t(Lub2) chromosome 17 variant contains a small deletion that removes at least seven genes including Igf2r. We have constructed a YAC contig spanning the entire t(Lub2) deletion and created a restriction map that covers 700 kb. The position, transcription orientation, and imprinted status of the genes immediately flanking Igf2r have been assessed. We show here that the Mas gene, which lies 65 kb upstream to Igf2r, contains a novel 5' exon and is not imprinted in adult tissues. We further show that the recently identified Lx1 gene lies immediately downstream and is also expressed from both parental alleles in adult tissues. The remaining genes in this region have previously been shown to be biallelically expressed.
- Max Planck Society Germany
- Netherlands Heart Institute Netherlands
- Max Planck Institute for Molecular Genetics Germany
- Erasmus University Rotterdam Netherlands
- Antoni van Leeuwenhoek Hospital Netherlands
Base Sequence, Molecular Sequence Data, Chromosome Mapping, Gene Expression, Gene Expression Regulation, Developmental, Membrane Proteins, Exons, Blotting, Northern, Cosmids, Proto-Oncogene Mas, Chromosomes, Genomic Imprinting, Mice, Genes, Animals, EMC MM-02-41-03, Cloning, Molecular, DNA Probes, Deoxyribonucleases, Type II Site-Specific, Chromosomes, Artificial, Yeast, Alleles
Base Sequence, Molecular Sequence Data, Chromosome Mapping, Gene Expression, Gene Expression Regulation, Developmental, Membrane Proteins, Exons, Blotting, Northern, Cosmids, Proto-Oncogene Mas, Chromosomes, Genomic Imprinting, Mice, Genes, Animals, EMC MM-02-41-03, Cloning, Molecular, DNA Probes, Deoxyribonucleases, Type II Site-Specific, Chromosomes, Artificial, Yeast, Alleles
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