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

作者: Diana Lucifero , J Richard Chaillet , Jacquetta M Trasler

DOI: 10.1093/HUMUPD/DMH002

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摘要: Recent studies suggest a possible link between human assisted reproductive technology and genomic imprinting disorders. Assisted includes the isolation, handling culture of gametes early embryos at times when imprinted genes are likely to be particularly vulnerable external influences. Evidence sex-specific differences in imprint acquisition suggests that male female germ cells may susceptible perturbations specific prenatal postnatal stages. Imprints acquired first during gametogenesis must maintained preimplantation development reprogramming overall genome occurs. In this review, we will discuss both new developments our understanding including mechanisms timing erasure, maintenance cell embryogenesis as well implications research for future epigenetic reproduction technology.

参考文章(148)
Wolf Reik, Jörn Walter, Evolution of imprinting mechanisms: the battle of the sexes begins in the zygote. Nature Genetics. ,vol. 27, pp. 255- 256 ,(2001) , 10.1038/85804
Yong-Kook Kang, Deog-Bon Koo, Jung-Sun Park, Young-Hee Choi, An-Sik Chung, Kyung-Kwang Lee, Yong-Mahn Han, Aberrant methylation of donor genome in cloned bovine embryos. Nature Genetics. ,vol. 28, pp. 173- 177 ,(2001) , 10.1038/88903
Osman El-Maarri, Karin Buiting, Edwin G Peery, Peter M Kroisel, Basak Balaban, Klaus Wagner, Bulent Urman, Julia Heyd, Christina Lich, Camilynn I Brannan, Jörn Walter, Bernhard Horsthemke, None, Maternal methylation imprints on human chromosome 15 are established during or after fertilization Nature Genetics. ,vol. 27, pp. 341- 344 ,(2001) , 10.1038/85927
Lorraine E. Young, Kenneth Fernandes, Tom G. McEvoy, Simon C. Butterwith, Carlos G. Gutierrez, Catherine Carolan, Peter J. Broadbent, John J. Robinson, Ian Wilmut, Kevin D. Sinclair, Epigenetic change in IGF2R is associated with fetal overgrowth after sheep embryo culture Nature Genetics. ,vol. 27, pp. 153- 154 ,(2001) , 10.1038/84769
François Fuks, Wendy A. Burgers, Alexander Brehm, Luke Hughes-Davies, Tony Kouzarides, DNA methyltransferase Dnmt1 associates with histone deacetylase activity. Nature Genetics. ,vol. 24, pp. 88- 91 ,(2000) , 10.1038/71750
Michael A. Preece, The genetics of the Silver-Russell syndrome. Reviews in Endocrine & Metabolic Disorders. ,vol. 3, pp. 369- 379 ,(2002) , 10.1023/A:1020961909991
Masaki Okano, Shaoping Xie, En Li, Cloning and characterization of a family of novel mammalian DNA (cytosine-5) methyltransferases Nature Genetics. ,vol. 19, pp. 219- 220 ,(1998) , 10.1038/890
Toshinobu Miyamoto, Shiga Hasuike, Yoshihiro Jinno, Hidenobu Soejima, Kankatsu Yun, Kiyonori Miura, Mutsuo Ishikawa, Norio Niikawa, The human ASCL2 gene escaping genomic imprinting and its expression pattern. Journal of Assisted Reproduction and Genetics. ,vol. 19, pp. 240- 244 ,(2002) , 10.1023/A:1015362903486
Louis Lefebvre, Stéphane Viville, Sheila C. Barton, Fumitoshi Ishino, Eric B. Keverne, M. Azim Surani, Abnormal maternal behaviour and growth retardation associated with loss of the imprinted gene Mest. Nature Genetics. ,vol. 20, pp. 163- 169 ,(1998) , 10.1038/2464
M. Brandeis, T. Kafri, M. Ariel, J.R. Chaillet, J. McCarrey, A. Razin, H. Cedar, The ontogeny of allele-specific methylation associated with imprinted genes in the mouse The EMBO Journal. ,vol. 12, pp. 3669- 3677 ,(1993) , 10.1002/J.1460-2075.1993.TB06041.X