Cell Resource Center for Biomedical Research, Institute of Development, Aging and Cancer, Tohoku University, Sendai, Miyagi, Japan.
Dev Growth Differ. 2010 Aug;52(6):517-25. doi: 10.1111/j.1440-169X.2010.01190.x.
Germ cells, after fate determination as primordial germ cells (PGCs) in early embryos, undergo various unique changes in epigenetic status during their development, and these changes differ from the epigenetic changes occurring in any other somatic cells. For example, PGCs undergo demethylation of DNA and change histone modification states on a genome-wide scale. Although the full physiological significance of these epigenetic alterations is still unclear, we can now discuss some of their mechanisms due to recent experimental evidence demonstrating the expression of candidate molecules involved in the processes of epigenetic change. On the other hand, DNA demethylation associated with PGC-specific gene expression, reprogramming of imprinted genes and regulation of retrotransposons in PGCs differentially occur from the genome-wide DNA demethylation. The tendency of epigenetic changes to appear on the whole genome, as well as more precise changes in the epigenetic status of particular parts of the genome, may play important roles in establishing the properties of PGCs required for acquiring totipotency.
生殖细胞在早期胚胎中被确定为原始生殖细胞(PGC)后,在其发育过程中经历了各种独特的表观遗传状态变化,这些变化与任何其他体细胞发生的表观遗传变化不同。例如,PGC 经历 DNA 的去甲基化和组蛋白修饰状态在全基因组范围内的改变。尽管这些表观遗传改变的全部生理意义尚不清楚,但由于最近的实验证据表明参与表观遗传变化过程的候选分子的表达,我们现在可以讨论其中的一些机制。另一方面,与 PGC 特异性基因表达、印迹基因重编程和 PGC 中逆转座子调控相关的 DNA 去甲基化与全基因组范围的 DNA 去甲基化不同。表观遗传变化倾向于在整个基因组上发生,以及基因组特定部分的表观遗传状态的更精确变化,可能在建立获得全能性所需的 PGC 特性方面发挥重要作用。