Gametes and embryo epigenetic reprogramming affect developmental outcome: implication for assisted reproductive technologies

作者: Saji Jacob , Kelle H Moley

DOI: 10.1203/01.PDR.0000179401.17161.D3

关键词:

摘要: There is concern about the health of children who are conceived with use assisted reproductive technologies (ART). In addition to reports low birth weight and chromosomal anomalies, there evidence that ART may be associated increased epigenetic disorders in infants using these procedures. Epigenetic reprogramming critical during gametogenesis at preimplantation stage involves DNA methylation, imprinting, RNA silencing, covalent modifications histones, remodeling by other chromatin-associated complexes. regulation involved early embryo development, fetal growth, weight. Disturbances lead developmental problems mortality. Recent suggest incidence imprinting such as Beckwith-Wiedemann syndrome, Angelman retinoblastoma ART. These result from an accumulation alterations culture and/or altered embryonic timing. Further research urgently needed determine whether a causal relationship between exists. Until then, cautious review both short-term long-term outcomes national level recommended.

参考文章(111)
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
Hugh D. Morgan, Heidi G.E. Sutherland, David I.K. Martin, Emma Whitelaw, Epigenetic inheritance at the agouti locus in the mouse Nature Genetics. ,vol. 23, pp. 314- 318 ,(1999) , 10.1038/15490
Rosalind M John, M Azim Surani, Agouti germ line gets acquisitive. Nature Genetics. ,vol. 23, pp. 254- 256 ,(1999) , 10.1038/15425
Ruthie E. Amir, Ignatia B. Van den Veyver, Mimi Wan, Charles Q. Tran, Uta Francke, Huda Y. Zoghbi, Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2. Nature Genetics. ,vol. 23, pp. 185- 188 ,(1999) , 10.1038/13810
Wendy P. Robinson, Susan L. Christian, Brian D. Kuchinka, Maria S. Peñaherrera, Soma Das, Simone Schuffenhauer, Susan Malcolm, Albert A. Schinzel, Terry J. Hassold, David H. Ledbetter, Somatic segregation errors predominantly contribute to the gain or loss of a paternal chromosome leading to uniparental disomy for chromosome 15. Clinical Genetics. ,vol. 57, pp. 349- 358 ,(2000) , 10.1034/J.1399-0004.2000.570505.X
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
Fang-Lin Sun, Wendy L. Dean, Gavin Kelsey, Nicholas D. Allen, Wolf Reik, Transactivation of Igf2 in a mouse model of Beckwith–Wiedemann syndrome Nature. ,vol. 389, pp. 809- 815 ,(1997) , 10.1038/39797
Déborah Bourc'his, Guo-Liang Xu, Chyuan-Sheng Lin, Brooke Bollman, Timothy H Bestor, Dnmt3L and the Establishment of Maternal Genomic Imprints Science. ,vol. 294, pp. 2536- 2539 ,(2001) , 10.1126/SCIENCE.1065848
Wolf Reik, Wendy Dean, Jorn Walter, Epigenetic Reprogramming in Mammalian Development Science. ,vol. 293, pp. 1089- 1093 ,(2001) , 10.1126/SCIENCE.1063443