Reproductive epigenetics

被引:55
作者
Kelly, TLJ
Trasler, JM
机构
[1] McGill Univ, Montreal Childrens Hosp, Res Inst, Montreal, PQ H3H 1P3, Canada
[2] McGill Univ, Dept Paediat, Montreal, PQ, Canada
[3] McGill Univ, Dept Human Genet, Montreal, PQ, Canada
[4] McGill Univ, Dept Pharmacol & Therapeut, Montreal, PQ, Canada
关键词
DNA methylation; epigenetics; gametogenesis; genomic imprinting; human; mouse; oocytes; oogenesis; preimplantation embryos; sperm; spermatogenesis;
D O I
10.1111/j.0009-9163.2004.00236.x
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Epigenetics refers to covalent modifications of DNA and core histones that regulate gene activity without altering DNA sequence. To date, the best-characterized DNA modification associated with the modulation of gene activity is methylation of cytosine residues within CpG dinucleotides. Human disorders associated with epigenetic abnormalities include rare imprinting diseases, molar pregnancies, and childhood cancers. Germ cell development and early embryo development are critical times when epigenetic patterns are initiated or maintained. This review focuses on the epigenetic modification DNA methylation and discusses recent progress that has been made in understanding when and how epigenetic patterns are differentially established in the male and female germlines, the mouse, and human disorders associated with abnormalities in epigenetic programming in germ cells and early embryos, as well as genetic and other modulators (e.g. nutrition and drugs) of reproductive epigenetic events.
引用
收藏
页码:247 / 260
页数:14
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