Patients with familial biparental hydatidiform moles have normal methylation at imprinted genes

被引:14
作者
El-Maarri, O
Seoud, M
Rivière, JB
Oldenburg, J
Walter, J
Rouleau, G
Slim, R
机构
[1] Inst Expt Haematol & Transfus Med, Bonn, Germany
[2] Amer Univ Beirut, Dept Obstet & Gynecol, Beirut, Lebanon
[3] Ctr Hosp Univ Montreal, Dept Med, Montreal, PQ, Canada
[4] Inst Transfus Med & Immunohaematol, Frankfurt, Germany
[5] Univ Saarland, Biosci Dept Genet Epigenet, D-6600 Saarbrucken, Germany
[6] McGill Univ, Ctr Hlth, Dept Human Genet & Obstet & Gynecol, Montreal, PQ, Canada
基金
加拿大健康研究院;
关键词
hydatidiform moles; molar pregnancy; methylation analysis; SIRPH; imprinting;
D O I
10.1038/sj.ejhg.5201353
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
In molar tissues from patients with recurrent biparental hydatidiform moles, we could previously demonstrate that differentially methylated regions (DMRs) of four imprinted genes are abnormally methylated on the maternal alleles. It remained unclear if this abnormal methylation originated de novo in the molar tissues or if it is even recognizable in the patient somatic tissues. To address this question, we investigated the DNA methylation of four imprinted genes in total blood from the two sister-patients. Here, we show that both patients retain normal methylation levels at the DMRs of the four genes in blood tissues. For two maternally expressed genes, we could use informative SNPs to follow the inheritance of the abnormally methylated maternal alleles in the molar tissues. We find that the transmitted abnormally methylated maternal alleles to the moles originated from the maternal grandmother and that the same alleles are not methylated in the patients. Our data suggest that the abnormal methylation in familial biparental molar tissues was acquired de novo in the patients'germline as a result of a false reprogramming or during the postzygotic development of the conceptuses that led to moles.
引用
收藏
页码:486 / 490
页数:5
相关论文
共 23 条
[1]  
Barro C, 2002, ANN BIOL CLIN-PARIS, V60, P325
[2]  
Cui HM, 2001, CANCER RES, V61, P4947
[3]   Maternal alleles acquiring paternal methylation patterns in biparental complete hydatidiform moles [J].
El-Maarri, O ;
Seoud, M ;
Coullin, P ;
Herbiniaux, U ;
Oldenburg, J ;
Rouleau, G ;
Slim, R .
HUMAN MOLECULAR GENETICS, 2003, 12 (12) :1405-1413
[4]   A rapid, quantitative, non-radioactive bisulfite-SNuPE-IP RP HPLC assay for methylation analysis at specific CpG sites [J].
El-Maarri, O ;
Herbiniaux, U ;
Walter, J ;
Oldenburg, J .
NUCLEIC ACIDS RESEARCH, 2002, 30 (06) :25
[5]  
El-Maarri Osman, 2004, Methods Mol Biol, V287, P195
[6]   The maternally transcribed gene p57KIP2 (CDNK1C) is abnormally expressed in both androgenetic and biparental complete hydatidiform moles [J].
Fisher, RA ;
Hodges, MD ;
Rees, HC ;
Sebire, NJ ;
Seckl, MJ ;
Newlands, ES ;
Genest, DR ;
Castrillon, DH .
HUMAN MOLECULAR GENETICS, 2002, 11 (26) :3267-3272
[7]   Loss of H19 imprinting and up-regulation of H19 and SNRPN in a case with malignant mixed Mullerian tumor of the uterus [J].
Hashimoto, K ;
Azuma, C ;
Tokugawa, Y ;
Nobunaga, T ;
Aki, TA ;
Matsui, Y ;
Yanagida, T ;
Izumi, H ;
Saji, F ;
Murata, Y .
HUMAN PATHOLOGY, 1997, 28 (07) :862-865
[8]   A global disorder of imprinting in the human female germ line [J].
Judson, H ;
Hayward, BE ;
Sheridan, E ;
Bonthron, DT .
NATURE, 2002, 416 (6880) :539-542
[9]  
KONDO M, 1995, ONCOGENE, V10, P1193
[10]  
Kumar K S D, 2003, J Obstet Gynaecol, V23, P55, DOI 10.1080/0144361021000043263