Université Clermont Auvergne, CNRS, Inserm, GReD, 63000, Clermont-Ferrand, France.
King's College, London, UK.
Cell Mol Life Sci. 2021 Jan;78(2):757-768. doi: 10.1007/s00018-020-03541-8. Epub 2020 May 14.
The acquisition of cell identity is associated with developmentally regulated changes in the cellular histone methylation signatures. For instance, commitment to neural differentiation relies on the tightly controlled gain or loss of H3K27me3, a hallmark of polycomb-mediated transcriptional gene silencing, at specific gene sets. The KDM6B demethylase, which removes H3K27me3 marks at defined promoters and enhancers, is a key factor in neurogenesis. Therefore, to better understand the epigenetic regulation of neural fate acquisition, it is important to determine how Kdm6b expression is regulated. Here, we investigated the molecular mechanisms involved in the induction of Kdm6b expression upon neural commitment of mouse embryonic stem cells. We found that the increase in Kdm6b expression is linked to a rearrangement between two 3D configurations defined by the promoter contact with two different regions in the Kdm6b locus. This is associated with changes in 5-hydroxymethylcytosine (5hmC) levels at these two regions, and requires a functional ten-eleven-translocation (TET) 3 protein. Altogether, our data support a model whereby Kdm6b induction upon neural commitment relies on an intronic enhancer the activity of which is defined by its TET3-mediated 5-hmC level. This original observation reveals an unexpected interplay between the 5-hmC and H3K27me3 pathways during neural lineage commitment in mammals. It also questions to which extent KDM6B-mediated changes in H3K27me3 level account for the TET-mediated effects on gene expression.
细胞特征的获得与细胞组蛋白甲基化特征的发育调控变化有关。例如,神经分化的决定依赖于特定基因集上 H3K27me3 的严格控制的获得或丢失,H3K27me3 是多梳介导的转录基因沉默的标志。KDM6B 去甲基酶可去除特定启动子和增强子上的 H3K27me3 标记,是神经发生的关键因素。因此,为了更好地理解神经命运获得的表观遗传调控,确定 Kdm6b 表达的调节方式非常重要。在这里,我们研究了在小鼠胚胎干细胞向神经分化时诱导 Kdm6b 表达的分子机制。我们发现,Kdm6b 表达的增加与启动子与 Kdm6b 基因座的两个不同区域之间的两种 3D 构象之间的重排有关。这与这两个区域的 5-羟甲基胞嘧啶(5hmC)水平的变化有关,并且需要功能性的 ten-eleven-translocation(TET)3 蛋白。总的来说,我们的数据支持这样一种模型,即在神经分化时诱导 Kdm6b 表达依赖于一个内含子增强子,其活性由其 TET3 介导的 5-hmC 水平定义。这一原始观察结果揭示了在哺乳动物神经谱系分化过程中,5-hmC 和 H3K27me3 途径之间的一种意想不到的相互作用。它还质疑 KDM6B 介导的 H3K27me3 水平变化在多大程度上解释了 TET 对基因表达的影响。