Genetic and Epigenetic Analysis of Recurrent Hydatidiform Mole

• Published in: Human mutation Vol. 30; no. 5; pp. E629 - E639
• Main Authors: Hayward, Bruce E, De Vos, Michel, Talati, Nargese, Abdollahi, M. Reza, Taylor, Graham R, Meyer, Esther, Williams, Denise, Maher, Eamonn R, Setna, Faridon, Nazir, Kausar, Hussaini, Shahnaz, Jafri, Hussain, Rashid, Yasmin, Sheridan, Eamonn, Bonthron, David T
• Format: Journal Article
• Language: English
• Published: Hoboken Wiley Subscription Services, Inc., A Wiley Company 01.05.2009
• Subjects: Adaptor Proteins, Signal Transducing - genetics; autosomal recessive; DNA Methylation; DNA Mutational Analysis; Epigenesis, Genetic; epigenetics; Evolution, Molecular; Female; Genomic Imprinting; Humans; hydatidiform mole; Hydatidiform Mole - genetics; imprinting; Mutation - genetics; NLRP7; Phylogeny; Pregnancy; Sequence Analysis, DNA; Uterine Neoplasms - genetics
• ISSN: 1059-7794; 1098-1004
• DOI: 10.1002/humu.20993

Familial biparental hydatidiform mole (FBHM) is a maternal-effect autosomal recessive disorder in which recurrent pregnancy failure with molar degeneration occurs. The phenotype mimics molar pregnancy due to androgenesis, despite the normal genetic makeup of the conceptus. FBHM appears to result from a failure to establish correct maternal epigenetic identity at imprinted loci during oogenesis. Several women affected with FBHM have previously been shown to have biallelic mutations in the NLRP7 gene (NALP7). Here, we present the results of epigenetic and mutational analysis on FBHM patients from 11 families, 10 of them novel. We demonstrate a methylation defect at imprinted loci in tissue from four new FBHM cases. Biallelic NLRP7 mutations, including eight previously undescribed mutations, were found in all but one family. These results indicate for the first time that maternal imprints at some loci may be correctly specified in FBHM conceptions, since differential methylation of SGCE/PEG10 was preserved in all four cases.