Beckwith-Wiedemann syndrome prenatal diagnosis by methylation analysis in chorionic villi

被引:24
|
作者
Paganini, Leda [1 ]
Carlessi, Nicole [1 ]
Fontana, Laura [1 ]
Silipigni, Rosamaria [2 ]
Motta, Silvia [2 ]
Fiori, Stefano [1 ]
Guerneri, Silvana [2 ]
Lalatta, Faustina [3 ]
Cereda, Anna [4 ]
Sirchia, Silvia [5 ]
Miozzo, Monica [1 ]
Tabano, Silvia [1 ]
机构
[1] Univ Milan, Fdn IRCCS Ca Granda Osped Maggiore Policlin, Dept Pathophysiol & Transplantat, Div Pathol, Milan, Italy
[2] Fdn IRCCS Ca Granda Osped Maggiore Policlin, Med Genet Lab, Milan, Italy
[3] Fdn IRCCS Ca Granda Osped Maggiore Policlin, Clin Genet Unit, Milan, Italy
[4] Azienda Osped Papa Giovanni XXIII, Pediat Unit, Bergamo, Italy
[5] Univ Milan, Dept Hlth Sci, Med Genet, Milan, Italy
关键词
Beckwith-Wiedemann syndrome; chorionic villi; DNA methylation; imprinting; prenatal diagnosis; ASSISTED REPRODUCTIVE TECHNOLOGY; FETAL-GROWTH; IMPRINTING DISORDERS; DNA METHYLATION; TRANSCRIPTION; REVEALS; ERRORS; GENE; ART;
D O I
10.1080/15592294.2015.1057383
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Beckwith-Wiedemann syndrome (BWS) is an imprinting disorder that can be prenatally suspected or diagnosed based on established clinical guidelines. Molecular confirmation is commonly performed on amniocytes. The possibility to use fresh (CVF) and cultured (CVC) chorionic villi has never been investigated. To verify whether CVF and CVC are reliable sources of DNA to study fetal methylation, we used pyrosequencing to test the methylation level of a number of differentially methylated regions (DMRs) at several imprinted loci (ICR1, ICR2, H19, PWS/AS-ICR, GNASXL, GNAS1A, ZAC/PLAGL1, and MEST) and at non-imprinted MGMT and RASSF1A promoters. We analyzed these regions in 19 healthy pregnancies and highlighted stable methylation levels between CVF and CVC at ICR1, ICR2, GNASXL, PWS/AS-ICR, and MEST. Conversely, the methylation levels at H19 promoter, GNAS1A and ZAC/PLAGL1 were different in CVC compared to fresh CV. We also investigated ICR1 and ICR2 methylation level of CVF/CVC of 2 BWS-suspected fetuses (P1 and P2). P1 showed ICR2 hypomethylation, P2 showed normal methylation at both ICR1 and ICR2. Our findings, although limited to one case of BWS fetus with an imprinting defect, can suggest that ICR1 and ICR2, but not H19, could be reliable targets for prenatal BWS diagnosis by methylation test in CVF and CVC. In addition, PWS/AS-ICR, GNASXL, and MEST, but not GNAS1A and ZAC/PLAGL1, are steadily hemimethylated in CV from healthy pregnancies, independently from culture. Thus, prenatal investigation of genomic imprinting in CV needs to be validated in a locus-specific manner.
引用
收藏
页码:643 / 649
页数:7
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