Epigenetic status of the H19 locus in human oocytes following in vitro maturation

被引:113
作者
Borghol, N
Lornage, J
Blachère, T
Garret, AS
Lefèvre, A
机构
[1] Hop Debrousse, UA 953, INRA, INSERM,U418, F-69322 Lyon 05, France
[2] Hop Edouard Herriot, Serv Med Reprod, F-69003 Lyon, France
关键词
human oocytes; in vitro maturation; imprinting; H19; methylation;
D O I
10.1016/j.ygeno.2005.10.008
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Imprinting is an epigenetic modification that is reprogrammed in the germ line and leads to the monoallelic expression of some genes. Imprinting involves DNA methylation. Maternal imprint is reset during oocyte growth and maturation. In vitro maturation (IVM) of oocytes may, therefore, interfere with imprint acquisition and/or maintenance. To evaluate if maturing human oocytes in vitro would be hazardous at the epigenetic level, we first determined the methylation profile of the H19 differentially methylated region (DMR). The methylation status of the H19 DMR seems particularly vulnerable to in vitro culture conditions. We analyzed oocytes at different stages of maturation following IVM, germinal vesicle (GV), metaphase I (MI), and metaphase II (MII), using the bisulfite mutagenesis technique. Our results indicated that the unmethylated specific maternal profile for the H19 DMR was stably established at the GV stage. The majority of MI-arrested oocytes exhibited an altered pattern of methylation, the CTCF-binding site being methylated in half of the DNA strands analyzed. Of the 20 MII oocytes analyzed, 15 showed the normal unmethylated maternal pattern, while 5 originating from two different patients exhibited a methylated pattern. These findings highlight the need for extended analysis on MII-rescued oocytes to appreciate the epigenetic safety of the IVM procedure, before it becomes a routine and practical assisted reproductive procedure. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:417 / 426
页数:10
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