Imprinted Segments in the Human Genome: Different Dna Methylation Patterns in the Prader-Willi/Angelman Syndrome Region As Determined by the Genomic Sequencing Method

Author： Zeschnigk Michael Schmitz Birgit Dittrich Bärbel Buiting Karin Horsthemke Bernhard Doerfler Walter

Publisher： Oxford University Press

ISSN： 1460-2083

Source： Human Molecular Genetics, Vol.6, Iss.3, 1997-01, pp. : 387-395

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Abstract

A deletion of 15q11-q13 and uniparental disomy 15 lead to Prader-Labhart-Willi syndrome (PWS) or Angelman syndrome (AS) because this region contains genes expressed exclusively from the paternal (PWS) or maternal (AS) chromosome, respectively. DNA methylation plays a role in the control of imprinted gene expression, but so far only a few 5′-CG-3′ dinucleotides within the recognition sites of the methylation sensitive enzymes have been studied. As part of a study on DNA methylation patterns in the human genome, we have applied the bisulfite protocol of genomic sequencing to study all 5′-CG-3′ dinucleotides around exon 1 of SNRPN and at the D15S63 locus, which contains a start site for alternative SNRPN transcripts possibly involved in imprint switching during gametogenesis. At least 17 PCR products derived from single chromosomes of normal individuals as well as PWS and AS patients have been sequenced. We have found that cytosine residues outside 5′-CG-3′ dinucleotides are always unmethylated. However, >96% of all of the 23 5′-CG-3′ dinucleotides around SNRPN exon 1 are methylated on the maternal chromosome and completely devoid of methylation on the paternal chromosome. This finding is in contrast to the D15S63 locus, where only the two CfoI/HhaI sites are methylated on the maternal chromosome at the same frequency as seen for the SNRPN segment. At the other five 5′-CG-3′ dinucleotides, differential methylation is less pronounced, i.e. 45–70% on the maternal chromosome and 5–14% on the paternal chromosome. The differences between SNRPN and D15S63 methylation may reflect different biological functions of the alternative SNRPN transcripts. The systematic investigation of 5′-CG-3′ methylation patterns as reported here will provide the basis for a PCR-based methylation test to diagnose PWS and AS.