Imprinting mutations suggested by abnormal DNA methylation patterns in familial Angelman and Prader-Willi syndromes

André Reis, Bärbel Dittrich, I. Valerie Greger, Karin Bulting, Marc Lalande, Gabriele Gillessen-Kaesbach, Maria Anvret, Bernhard Horsthemke*

*Corresponding author for this work
179 Citations (Scopus)

Abstract

The D15S9 and D15S63 loci in the Prader-Willi/Angelman syndrome region on chromosome 15 are subject to parent-of-origin-specific DNA methylation. We have found two Prader-Willi syndrome families in which the patients carry a maternal methylation imprint on the paternal chromosome. In one of these families, the patients have a small deletion encompassing the gene for the small nuclear ribonucleoprotein polypeptide N, which maps 130 kb telomeric to D15S63. Furthermore, we have identified a pair of nondeletion Angelman syndrome sibs and two isolated Angelman syndrome patients who carry a paternal methylation imprint on the maternal chromosome. These Angelman and Prader-Willi syndrome patients may have a defect in the imprinting process in 15q11-13. We propose a model in which a cis-acting mutation prevents the resetting of the imprinting signal in the germ line and thus disturbs the expression of imprinted genes in this region.

Original languageEnglish
JournalAmerican Journal of Human Genetics
Volume54
Issue number5
Pages (from-to)741-747
Number of pages7
ISSN0002-9297
Publication statusPublished - 1994

Research Areas and Centers

  • Research Area: Medical Genetics

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