Department of Reproduction and Development, Erasmus MC, University Medical Center, Rotterdam, The Netherlands.
PLoS Genet. 2011 Jan 27;7(1):e1002001. doi: 10.1371/journal.pgen.1002001.
In somatic cells of female placental mammals, one of the two X chromosomes is transcriptionally silenced to accomplish an equal dose of X-encoded gene products in males and females. Initiation of random X chromosome inactivation (XCI) is thought to be regulated by X-encoded activators and autosomally encoded suppressors controlling Xist. Spreading of Xist RNA leads to silencing of the X chromosome in cis. Here, we demonstrate that the dose dependent X-encoded XCI activator RNF12/RLIM acts in trans and activates Xist. We did not find evidence for RNF12-mediated regulation of XCI through Tsix or the Xist intron 1 region, which are both known to be involved in inhibition of Xist. In addition, we found that Xist intron 1, which contains a pluripotency factor binding site, is not required for suppression of Xist in undifferentiated ES cells. Analysis of female Rnf12⁻/⁻ knockout ES cells showed that RNF12 is essential for initiation of XCI and is mainly involved in the regulation of Xist. We conclude that RNF12 is an indispensable factor in up-regulation of Xist transcription, thereby leading to initiation of random XCI.
在雌性胎盘哺乳动物的体细胞中,两条 X 染色体中的一条被转录沉默,以在男性和女性中实现等量的 X 染色体编码基因产物。随机 X 染色体失活 (XCI) 的起始被认为受到 X 染色体编码激活子和控制 Xist 的常染色体编码抑制剂的调节。Xist RNA 的扩散导致顺式 X 染色体沉默。在这里,我们证明剂量依赖性 X 染色体编码 XCI 激活因子 RNF12/RLIM 以反式作用并激活 Xist。我们没有发现 RNF12 通过 Tsix 或 Xist 内含子 1 区域介导 XCI 调节的证据,已知这两个区域都参与抑制 Xist。此外,我们发现包含多能因子结合位点的 Xist 内含子 1 对于未分化的 ES 细胞中 Xist 的抑制不是必需的。对雌性 Rnf12⁻/⁻ 敲除 ES 细胞的分析表明,RNF12 对于 XCI 的起始是必不可少的,并且主要参与 Xist 的调节。我们得出结论,RNF12 是上调 Xist 转录的不可或缺的因素,从而导致随机 XCI 的起始。