Potential significance of genomic imprinting defects for reproduction and assisted reproductive technology

被引:147
作者
Lucifero, D
Chaillet, JR
Trasler, JM
机构
[1] McGill Univ, Montreal Childrens Hosp, Res Inst, Montreal, PQ H3H 1P3, Canada
[2] McGill Univ, Dept Paediat, Montreal, PQ H3H 1P3, Canada
[3] McGill Univ, Dept Human Genet, Montreal, PQ H3H 1P3, Canada
[4] McGill Univ, Dept Pharmacol & Therapeut, Montreal, PQ H3H 1P3, Canada
[5] Univ Pittsburgh, Dept Mol Genet & Biochem, Pittsburgh, PA 15213 USA
关键词
Angelman syndrome; assisted reproductive technology; Beckwith-Wiedemann syndrome; genomic imprinting; reproduction;
D O I
10.1093/humupd/dmh002
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Recent studies suggest a possible link between human assisted reproductive technology and genomic imprinting disorders. Assisted reproductive technology includes the isolation, handling and culture of gametes and early embryos at times when imprinted genes are likely to be particularly vulnerable to external influences. Evidence of sex-specific differences in imprint acquisition suggests that male and female germ cells may be susceptible to perturbations in imprinted genes at specific prenatal and postnatal stages. Imprints acquired first during gametogenesis must be maintained during preimplantation development when reprogramming of the overall genome occurs. In this review, we will discuss both new developments in our understanding of genomic imprinting including the mechanisms and timing of imprint erasure, acquisition and maintenance during germ cell development and early embryogenesis as well as the implications of this research for future epigenetic studies in reproduction and assisted reproductive technology.
引用
收藏
页码:3 / 18
页数:16
相关论文
共 148 条
[71]   Risk of cancer in the offspring of women who underwent ovarian stimulation for IVF [J].
Klip, H ;
Burger, CW ;
de Kraker, J ;
van Leeuwen, FE .
HUMAN REPRODUCTION, 2001, 16 (11) :2451-2458
[72]   Epigenetic modifications during oocyte growth correlates with extended parthenogenetic development in the mouse [J].
Kono, T ;
Obata, Y ;
Yoshimzu, T ;
Nakahara, T ;
Carroll, J .
NATURE GENETICS, 1996, 13 (01) :91-94
[73]   Obstetric outcome of singleton pregnancies after IVF: a matched control study in four Dutch university hospitals [J].
Koudstaal, J ;
Braat, DDM ;
Bruinse, HW ;
Naaktgeboren, N ;
Vermeiden, JPW ;
Visser, GHA .
HUMAN REPRODUCTION, 2000, 15 (08) :1819-1825
[74]  
Lee J, 2002, DEVELOPMENT, V129, P1807
[75]   Abnormal maternal behaviour and growth retardation associated with loss of the imprinted gene Mest [J].
Lefebvre, L ;
Viville, S ;
Barton, SC ;
Ishino, F ;
Keverne, EB ;
Surani, MA .
NATURE GENETICS, 1998, 20 (02) :163-169
[76]  
Lei H, 1996, DEVELOPMENT, V122, P3195
[77]   TARGETED MUTATION OF THE DNA METHYLTRANSFERASE GENE RESULTS IN EMBRYONIC LETHALITY [J].
LI, E ;
BESTOR, TH ;
JAENISCH, R .
CELL, 1992, 69 (06) :915-926
[78]   ROLE FOR DNA METHYLATION IN GENOMIC IMPRINTING [J].
LI, E ;
BEARD, C ;
JAENISCH, R .
NATURE, 1993, 366 (6453) :362-365
[79]   Current understandings of the molecular genetics of gestational trophoblastic diseases [J].
Li, HW ;
Tsao, SW ;
Cheung, ANY .
PLACENTA, 2002, 23 (01) :20-31
[80]   Regulation of maternal behavior and offspring growth by paternally expressed Peg3 [J].
Li, LL ;
Keverne, EB ;
Aparicio, SA ;
Ishino, F ;
Barton, SC ;
Surani, MA .
SCIENCE, 1999, 284 (5412) :330-333