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Hum Mol Genet ; 4(9): 1499-507, 1995 Sep.
Article in English | MEDLINE | ID: mdl-8541832

ABSTRACT

The closely linked IGF2 and H19 genes on human chromosome 11p15.5 are monoallelically expressed as a result of genomic imprinting and show altered expression in Wilms' tumors (WTs). To map regional imprinting we have sought to isolate additional human genes close to IGF2/H19 and to characterize their allelic expression patterns. Here we report a novel gene, provisionally named L23MRP [L23 (mitochondrial)-related protein], which is oriented 'tail-to-tail' with H19 and is transcribed to within 40 kb of the last H19 exon. L23MRP is expressed biallelically in many mid-fetal and adult human tissues. This gene is also expressed at normal levels in WTs which have lost expression of H19 either via loss of the maternal chromosome 11p15.5 or via an epigenetic pathway involving site-specific DNA hypermethylation. These data indicate that, at least in post-embryonic stages, L23MRP is functionally insulated from the IGF2/H19 imprinted domain.


Subject(s)
Fetus/metabolism , Gene Expression Regulation, Developmental , Genomic Imprinting , Muscle Proteins/genetics , Proteins/genetics , RNA, Untranslated , Adult , Alleles , Amino Acid Sequence , Base Sequence , Cloning, Molecular , DNA/metabolism , DNA, Complementary , Humans , Methylation , Mitochondrial Proteins , Molecular Sequence Data , Polymorphism, Genetic , RNA, Long Noncoding , RNA, Messenger/genetics , RNA, Messenger/metabolism , RNA-Binding Proteins , Ribosomal Proteins , Sequence Homology, Amino Acid
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