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Demethylation of repetitive DNA sequences in neuroblastoma
Author(s) -
Thoraval Didier,
Asakawa Junichi,
Wimmer Katharina,
Kuick Rork,
Lamb Barbara,
Richardson Bruce,
Ambros Peter,
Glover Thomas,
Hanash Samir
Publication year - 1996
Publication title -
genes, chromosomes and cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.754
H-Index - 119
eISSN - 1098-2264
pISSN - 1045-2257
DOI - 10.1002/(sici)1098-2264(199612)17:4<234::aid-gcc5>3.0.co;2-4
Subject(s) - dna methylation , biology , neuroblastoma , methylation , genomic dna , epigenetics , dna demethylation , dna , genetics , restriction enzyme , gene , genomic imprinting , cancer , microbiology and biotechnology , gene expression , cell culture
Abstract Altered genomic methylcytosine content has been described for a number of tumor types, including neuroblastoma. However, it remains to be determined for different tumor types whether specific loci or chromosomal regions are affected by a methylation change or whether the change is random. We have implemented a computer‐based approach for the analysis of two‐dimensional separations of human genomic restriction fragments. Through the use of methylation‐sensitive restriction enzymes, methylation differences in genomic DNA between tumor and normal tissues can be detected. We report the cloning and sequencing of two fragments detectable in two‐dimensional separations of genomic DNA of neuroblastomas. These fragments were found to be a part of repetitive units that exhibited demethylation in neuroblastoma relative to other tumor types. Our finding of a distinct pattern of methylation of repetitive units in neuroblastoma suggests that altered methylation at certain loci may contribute to the biology of this tumor. Genes Chromosom Cancer 17:234–244 (1996). © 1996 Wiley‐Liss, Inc.