Monk M, Boubelik M, Lehnert S
MRC Mammalian Development Unit, University College London, UK.
Development. 1987 Mar;99(3):371-82. doi: 10.1242/dev.99.3.371.
This paper shows stage- and tissue-specific global demethylation and remethylation occurring during embryonic development. The egg genome is strikingly undermethylated and the sperm genome relatively methylated. Following a loss of genomic methylation during preimplantation development, embryonic and extraembryonic lineages are progressively and independently methylated to different final extents. Methylation continues postgastrulation and hence could be a mechanism initiating, or confirming, differential programming in the definitive germ layers. It is proposed that much of the methylation observed in somatic tissues acts to stabilize and reinforce prior events that regulate the activity of specific genes, chromosome domains or the X chromosome (in females). Fetal germ cell DNA is markedly undermethylated and we favour the idea that the germ lineage is set aside before the occurrence of extensive methylation of DNA in fetal precursor cells.
本文显示了胚胎发育过程中发生的阶段和组织特异性的全基因组去甲基化和重新甲基化。卵子基因组显著低甲基化,而精子基因组相对甲基化。在植入前发育过程中基因组甲基化缺失后,胚胎和胚外谱系逐渐且独立地甲基化至不同的最终程度。甲基化在原肠胚形成后仍持续存在,因此可能是启动或确认定形胚层中差异编程的一种机制。有人提出,在体细胞组织中观察到的大部分甲基化作用是稳定和加强先前调节特定基因、染色体结构域或X染色体(女性)活性的事件。胎儿生殖细胞DNA明显低甲基化,我们倾向于认为生殖谱系在胎儿前体细胞DNA广泛甲基化之前就已被区分出来。