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Gewählte Publikation:

El-Maarri, O; Buiting, K; Peery, EG; Kroisel, PM; Balaban, B; Wagner, K; Urman, B; Heyd, J; Lich, C; Brannan, CI; Walter, J; Horsthemke, B.
Maternal methylation imprints on human chromosome 15 are established during or after fertilization.
Nat Genet. 2001; 27(3):341-344 Doi: 10.1038/85927
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Co-Autor*innen der Med Uni Graz
Kroisel Peter
Wagner Klaus
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Abstract:
Prader-Willi syndrome (PWS) is a neurogenetic disorder that results from the lack of transcripts expressed from the paternal copy of the imprinted chromosomal region 15q11-q13 (refs. 1,2). In some patients, this is associated with a deletion of the SNURF-SNRPN exon 1 region inherited from the paternal grandmother and the presence of a maternal imprint on the paternal chromosome. Assuming that imprints are reset in the germ line, we and others have suggested that this region constitutes part of the 15q imprinting center (IC) and is important for the maternal to paternal imprint switch in the male germ line. Here we report that sperm DNA from two males with an IC deletion had a normal paternal methylation pattern along 15q11-q13. Similar findings were made in a mouse model. Our results indicate that the incorrect maternal methylation imprint in IC deletion patients is established de novo after fertilization. Moreover, we found that CpG-rich regions in SNURF-SNRPN and NDN, which in somatic tissues are methylated on the maternal allele, are hypomethylated in unfertilized human oocytes. Our results indicate that the normal maternal methylation imprints in 15q11-q13 also are established during or after fertilization.
Find related publications in this database (using NLM MeSH Indexing)
Animals -
Base Sequence -
Chromosomes, Human, Pair 15 - genetics
DNA - chemistry
DNA Methylation - chemistry
DNA Primers - genetics
Female - genetics
Fertilization - genetics
Genomic Imprinting - genetics
Humans - genetics
Male - genetics
Mice - genetics
Pedigree - genetics
Prader-Willi Syndrome - genetics
Pregnancy - genetics

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