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Projekt Druckansicht

DNA-Methylierungsanalyse von Imprints in gesunden, mittels assistierter Reproduktion gezeugter Kinder

Fachliche Zuordnung Humangenetik
Förderung Förderung von 2006 bis 2010
Projektkennung Deutsche Forschungsgemeinschaft (DFG) - Projektnummer 24327737
 
Erstellungsjahr 2010

Zusammenfassung der Projektergebnisse

Assisted reproductive technologies (ART) such as in vitro fertilization (IVF) and intracytoplasmic sperm injection (ICSI) are believed to destabilize genomic imprints. An increased frequency of Beckwith-Wiedemann syndrome in children born after ART has been reported. Other, mostly epidemiological, studies argue against this finding. The aim of this study was to examine the effect of ART on the stability of DNA methylation imprints. DNA was extracted from maternal peripheral blood (MPB), umbilical cord blood (UCB) and amnion/chorion tissue (ACT) of 185 phenotypically normal children (77 ICSI, 35 IVF and 73 spontaneous conceptions). Using bisulphite-based technologies we analysed ten differentially methylated regions (DMRs) including KvDMRl, H19, SNRPN, MEST, GRB10, DLKI/MEG3 IG-DMR, GNAS NESP55, GNAS NESPas, GNAS XL-alpha-s and GNAS ExonlA. Methylation indices (MI) do not reveal any significant differences at nine DMRs among the conception groups in neither MPB, UCB nor in ACT. The only slightly variable DMR was that of MEST. Here the mean MI was higher in UCB and MPB of IVF cases (mean MI±SD: 0.41±0.03 (UCB) and 0.40±0.03 (MPB)) compared to the ICSI (0.38±0.03, p=0.003 (UCB); 0.37±0.04, p=0.0007 (MPB)) or spontaneous cases (0.38±0.03, p=0.003 (UCB); 0.38±0.04, p=0.02 (MPB)). Weak but suggestive correlations between DMRs were however found between MPB, UCB and ACT. In conclusion our study supports the notion that children conceived by ART do not show a higher degree of imprint variability and hence do not have an a priori higher risk for imprinting disorders.

Projektbezogene Publikationen (Auswahl)

  • Assisted reproductive technologies do not enhance the variability of DNA methylation imprints in human. J Med Genet 2010;47:371-6
    S. Tierling, N.Y. Souren, J. Gries, C. Lo Porto, M. Groth, P. Lutsik, H. Neitzel, I. Utz-Billing, G. Gillessen-Kaesbach, H. Kentenich, G. Griesinger, K. Sperling, E. Schwinger, J. Walter
 
 

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