Koike Tasuku, Wakai Takuya, Jincho Yuko, Sakashita Akihiko, Kobayashi Hisato, Mizutani Eiji, Wakayama Sayaka, Miura Fumihito, Ito Takashi, Kono Tomohiro
Department of Bioscience, Tokyo University of Agriculture, Tokyo, Japan.
NODAI Genome Research Center, Tokyo University of Agriculture, Tokyo, Japan.
Biol Reprod. 2016 Jun;94(6):128. doi: 10.1095/biolreprod.116.138677. Epub 2016 Apr 20.
The germ line reprogramming barrier resets parental epigenetic modifications according to sex, conferring totipotency to mammalian embryos upon fertilization. However, it is not known whether epigenetic errors are committed during germ line reprogramming that are then transmitted to germ cells, and consequently to offspring. We addressed this question in the present study by performing a genome-wide DNA methylation analysis using a target postbisulfite sequencing method in order to identify DNA methylation errors in cloned mouse sperm. The sperm genomes of two somatic cell-cloned mice (CL1 and CL7) contained significantly higher numbers of differentially methylated CpG sites (P = 0.0045 and P = 0.0116). As a result, they had higher numbers of differentially methylated CpG islands. However, there was no evidence that these sites were transmitted to the sperm genome of offspring. These results suggest that DNA methylation errors resulting from embryo cloning are transmitted to the sperm genome by evading the germ line reprogramming barrier.
生殖系重编程屏障会根据性别重置亲代的表观遗传修饰,使哺乳动物胚胎在受精时具备全能性。然而,目前尚不清楚在生殖系重编程过程中是否会出现表观遗传错误,这些错误随后会传递给生殖细胞,进而传递给后代。在本研究中,我们通过使用目标亚硫酸氢盐测序方法进行全基因组DNA甲基化分析,以确定克隆小鼠精子中的DNA甲基化错误,从而解决了这个问题。两只体细胞克隆小鼠(CL1和CL7)的精子基因组中,差异甲基化CpG位点的数量显著更高(P = 0.0045和P = 0.0116)。结果,它们具有更多的差异甲基化CpG岛。然而,没有证据表明这些位点会传递给后代的精子基因组。这些结果表明,胚胎克隆导致的DNA甲基化错误通过避开生殖系重编程屏障传递到精子基因组中。