Genetics and Genome Biology, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada.
Fertil Steril. 2013 Mar 1;99(3):607-15. doi: 10.1016/j.fertnstert.2013.01.117. Epub 2013 Jan 26.
Several types of epigenetic marks facilitate the complex patterning required for normal human development. These epigenetic marks include DNA methylation at CpG dinucleotides, covalent modifications of histone proteins, and noncoding RNAs (ncRNAs). They function in a highly orchestrated manner, regulating mitotically heritable differences in gene expression potential without altering the primary DNA sequence. In germ cells and the developing embryo, genome-wide epigenetic reprogramming drives the erasure and reestablishment of correct epigenetic patterns at critical developmental time periods and in specific cell types. Two specific types of epigenetic regulation established in early development include X-chromosome inactivation and genomic imprinting; they regulate gene expression in a dosage-dependent and parent-of-origin-specific manner, respectively. Both genetic and environmental factors impact epigenetic marks, generating phenotypic variation that ranges from normal variation to human disease. Aberrant epigenetic patterning can lead to a variety of human disorders, including subfertility and imprinting disorders.
几种类型的表观遗传标记有助于促进正常人类发育所需的复杂模式。这些表观遗传标记包括 CpG 二核苷酸的 DNA 甲基化、组蛋白的共价修饰和非编码 RNA(ncRNA)。它们以高度协调的方式发挥作用,调节有丝分裂遗传的基因表达潜力差异,而不改变主要 DNA 序列。在生殖细胞和发育中的胚胎中,全基因组表观遗传重编程驱动关键发育时期和特定细胞类型中正确的表观遗传模式的消除和重新建立。在早期发育中建立的两种特定类型的表观遗传调控包括 X 染色体失活和基因组印记;它们分别以剂量依赖和亲本来源特异性的方式调节基因表达。遗传和环境因素都会影响表观遗传标记,从而产生从正常变异到人类疾病的表型变异。异常的表观遗传模式会导致多种人类疾病,包括不孕和印记疾病。