Torres-Padilla Maria-Elena, Bannister Andrew J, Hurd Paul J, Kouzarides Tony, Zernicka-Goetz Magdalena
The Wellcome Trust/Cancer Research UK Gurdon Institute, University of Cambridge, U.K.
Int J Dev Biol. 2006;50(5):455-61. doi: 10.1387/ijdb.052073mt.
Upon fertilization, the gametes undergo a drastic reprogramming that includes changes in DNA methylation and histone modifications. Currently, it is not known whether replacement of the major histones by histone variants is also involved in these processes. Here we have examined the expression and localization of the histone variant H3.3 in early mouse embryogenesis. We show that H3.3 is present in the oocyte as a maternal factor. It is then incorporated preferentially into the male pronucleus before genome activation, pointing towards an asymmetry in histone composition between the two pronuclei. This is in line with the male pronucleus bearing transcriptional activation first. The same distribution was observed when we followed the localisation of a tagged version of H3.3. We detected H3.3 in the nuclei of mouse embryos in all of the stages analysed, from the zygote to the blastocyst stage, suggesting that the epigenetic mechanisms in the early embryo not only involve changes in histone modifications but may also include histone replacement.
受精时,配子会经历剧烈的重编程,包括DNA甲基化和组蛋白修饰的变化。目前,尚不清楚组蛋白变体取代主要组蛋白是否也参与这些过程。在这里,我们研究了组蛋白变体H3.3在小鼠早期胚胎发育中的表达和定位。我们发现H3.3作为母体因子存在于卵母细胞中。然后,在基因组激活之前,它优先整合到雄原核中,这表明两个原核之间组蛋白组成存在不对称性。这与雄原核首先进行转录激活是一致的。当我们追踪标记版本的H3.3的定位时,观察到了相同的分布。我们在从受精卵到囊胚阶段的所有分析阶段的小鼠胚胎细胞核中都检测到了H3.3,这表明早期胚胎中的表观遗传机制不仅涉及组蛋白修饰的变化,还可能包括组蛋白替换。