Epigenetics and assisted reproductive technology: A call for investigation

被引:241
作者
Niemitz, EL
Feinberg, AP
机构
[1] Johns Hopkins Univ, Sch Med, Predoctoral Program Human Genet, Baltimore, MD 21205 USA
[2] Johns Hopkins Univ, Sch Med, Epigenet Unit, Dept Med, Baltimore, MD 21205 USA
[3] Johns Hopkins Univ, Sch Med, Epigenet Unit, Dept Mol Biol & Genet, Baltimore, MD 21205 USA
[4] Johns Hopkins Univ, Sch Med, Dept Oncol, Baltimore, MD 21205 USA
关键词
D O I
10.1086/382897
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
A surprising set of recent observations suggests a link between assisted reproductive technology ( ART) and epigenetic errors - that is, errors involving information other than DNA sequence that is heritable during cell division. An apparent association with ART was found in registries of children with Beckwith-Wiedemann syndrome, Angelman syndrome, and retinoblastoma. Here, we review the epidemiology and molecular biology behind these studies and those of relevant model systems, and we highlight the need for investigation of two major questions: (1) large-scale case-control studies of ART outcomes, including long-term assessment of the incidence of birth defects and cancer, and ( 2) investigation of the relationship between epigenetic errors in both offspring and parents, the specific methods of ART used, and the underlying infertility diagnoses. In addition, the components of proprietary commercial media used in ART procedures must be fully and publicly disclosed, so that factors such as methionine content can be assessed, given the relationship in animal studies between methionine exposure and epigenetic changes.
引用
收藏
页码:599 / 609
页数:11
相关论文
共 106 条
[1]   Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2 [J].
Amir, RE ;
Van den Veyver, IB ;
Wan, M ;
Tran, CQ ;
Francke, U ;
Zoghbi, HY .
NATURE GENETICS, 1999, 23 (02) :185-188
[2]   Congenital malformations in 4224 children conceived after IVF [J].
Anthony, S ;
Buitendijk, SE ;
Dorrepaal, CA ;
Lindner, K ;
Braat, DDM ;
den Ouden, AL .
HUMAN REPRODUCTION, 2002, 17 (08) :2089-2095
[3]   THE MOUSE INSULIN-LIKE GROWTH-FACTOR TYPE-2 RECEPTOR IS IMPRINTED AND CLOSELY LINKED TO THE TME LOCUS [J].
BARLOW, DP ;
STOGER, R ;
HERRMANN, BG ;
SAITO, K ;
SCHWEIFER, N .
NATURE, 1991, 349 (6304) :84-87
[4]   PHYSICAL MAP AROUND THE RETINOBLASTOMA GENE - POSSIBLE GENOMIC IMPRINTING SUGGESTED BY NRUI DIGESTION [J].
BLANQUET, V ;
TURLEAU, C ;
DEGROUCHY, J ;
CREAUGOLDBERG, N .
GENOMICS, 1991, 10 (02) :350-355
[5]   Dnmt3L and the establishment of maternal genomic imprints [J].
Bourc'his, D ;
Xu, GL ;
Lin, CS ;
Bollman, B ;
Bestor, TH .
SCIENCE, 2001, 294 (5551) :2536-2539
[6]   Sporadic imprinting defects in Prader-Willi syndrome and Angelman syndrome:: Implications for imprint-switch models, genetic counseling, and prenatal diagnosis [J].
Buiting, K ;
Dittrich, B ;
Gross, S ;
Lich, C ;
Färber, C ;
Buchholz, T ;
Smith, E ;
Reis, A ;
Bürger, J ;
Nöthen, MM ;
Barth-Witte, U ;
Janssen, B ;
Abeliovich, D ;
Lerer, I ;
van den Ouweland, AMW ;
Halley, DJJ ;
Schrander-Stumpel, C ;
Smeets, H ;
Meinecke, P ;
Malcolm, S ;
Gardner, A ;
Lalande, M ;
Nicholls, RD ;
Friend, K ;
Schulze, A ;
Matthijs, G ;
Kokkonen, H ;
Hilbert, P ;
Van Maldergem, L ;
Glover, G ;
Carbonell, P ;
Willems, P ;
Gillessen-Kaesbach, G ;
Horsthemke, B .
AMERICAN JOURNAL OF HUMAN GENETICS, 1998, 63 (01) :170-180
[7]   INHERITED MICRODELETIONS IN THE ANGELMAN AND PRADER-WILLI SYNDROMES DEFINE AN IMPRINTING CENTER ON HUMAN-CHROMOSOME-15 [J].
BUITING, K ;
SAITOH, S ;
GROSS, S ;
DITTRICH, B ;
SCHWARTZ, S ;
NICHOLLS, RD ;
HORSTHEMKE, B .
NATURE GENETICS, 1995, 9 (04) :395-400
[8]   BOVINE EMBRYO COCULTURE [J].
CATT, JW .
CELL BIOLOGY INTERNATIONAL, 1994, 18 (12) :1155-1162
[9]   DIFFERENTIAL ACTIVITY OF MATERNALLY AND PATERNALLY DERIVED CHROMOSOME REGIONS IN MICE [J].
CATTANACH, BM ;
KIRK, M .
NATURE, 1985, 315 (6019) :496-498
[10]   Angelman syndrome: a review of the clinical and genetic aspects [J].
Clayton-Smith, J ;
Laan, L .
JOURNAL OF MEDICAL GENETICS, 2003, 40 (02) :87-95