Shibata H, Ueda T, Kamiya M, Yoshiki A, Kusakabe M, Plass C, Held W A, Sunahara S, Katsuki M, Muramatsu M, Hayashizaki Y
RIKEN Tsukuba Life Science Center, The Institute of Physical and Chemical Research (RIKEN), 3-1-1 Koyadai, Tsukuba, Ibaraki, 305, Japan.
Genomics. 1997 Sep 1;44(2):171-8. doi: 10.1006/geno.1997.4877.
An oocyte-specific methylation imprint mark region, consisting of approximately 200 bp from the mouse imprinted gene U2afbp-rs, was identified within an area containing a CpG island and a short tandem repeat sequence. The oocyte-specific methylation was preserved in fertilized eggs and then expanded on the repressed maternal allele during preimplantation development until the adult methylation pattern was achieved by 12.5 days of embryonic development. These results indicate that the oocyte-specific imprinting mark region acts as a center in establishing the hypermethylated region on the repressed maternal allele. Furthermore, a region that is hypermethylated in both gametes was identified but its hypermethylation was conserved only on the maternal allele during preimplantation development, suggesting that some factor(s) inherited from oocytes may act to maintain hypermethylation on the maternal allele.
在一个包含CpG岛和短串联重复序列的区域内,鉴定出了一个卵母细胞特异性甲基化印记标记区域,该区域由来自小鼠印记基因U2afbp-rs的约200 bp组成。卵母细胞特异性甲基化在受精卵中得以保留,然后在植入前发育过程中在受抑制的母本等位基因上扩展,直到胚胎发育12.5天时达到成年甲基化模式。这些结果表明,卵母细胞特异性印记标记区域在建立受抑制母本等位基因上的高甲基化区域中起中心作用。此外,还鉴定出了一个在两种配子中均为高甲基化的区域,但其高甲基化仅在植入前发育过程中的母本等位基因上得以保留,这表明从卵母细胞继承的某些因子可能起到维持母本等位基因高甲基化的作用。