Department of Reproduction and Development, Room Ee 09-71, Erasmus MC, PO Box 2040, 3000 CA Rotterdam, The Netherlands.
Exp Cell Res. 2010 Mar 10;316(5):679-87. doi: 10.1016/j.yexcr.2010.01.015. Epub 2010 Jan 18.
In female somatic cells of mammalian species one X chromosome is inactivated to ensure dosage equality of X-encoded genes between females and males, during development and adulthood. X chromosome inactivation (XCI) involves various epigenetic mechanisms, including RNA mediated gene silencing in cis, DNA methylation, and changes in chromatin modifications and composition. XCI therefore provides an attractive paradigm to study epigenetic gene regulation in a more general context. The XCI process starts with counting of the number of X chromosomes present in a nucleus, and initiation of XCI follows if this number exceeds one per diploid genome. Recently, X-encoded RNF12 has been identified as a dose-dependent activator of XCI. In addition, other factors, including the pluripotency factors OCT4, SOX2 and Nanog, have been implicated to play a role in suppression of initiation of XCI. In this review, we highlight and explain these new and old findings in the context of a stochastic model for X chromosome counting and XCI initiation.
在哺乳动物的雌性体细胞中,一条 X 染色体失活,以确保雌性和雄性之间 X 染色体编码基因的剂量平衡,这一过程发生在发育和成年阶段。X 染色体失活(XCI)涉及多种表观遗传机制,包括顺式的 RNA 介导的基因沉默、DNA 甲基化,以及染色质修饰和组成的变化。因此,XCI 为在更广泛的背景下研究表观遗传基因调控提供了一个有吸引力的范例。XCI 过程始于对细胞核中存在的 X 染色体数量进行计数,如果该数量超过二倍体基因组中的一条,则启动 XCI。最近,X 染色体编码的 RNF12 被确定为 XCI 的剂量依赖性激活因子。此外,其他因素,包括多能性因子 OCT4、SOX2 和 Nanog,也被认为在抑制 XCI 的启动中发挥作用。在这篇综述中,我们将在 X 染色体计数和 XCI 启动的随机模型的背景下,强调和解释这些新的和旧的发现。