Stowers Institute for Medical Research, Kansas City, Missouri, USA.
Nat Struct Mol Biol. 2013 Sep;20(9):1093-7. doi: 10.1038/nsmb.2653. Epub 2013 Aug 11.
Promoters of many developmentally regulated genes, in the embryonic stem cell state, have a bivalent mark of H3K27me3 and H3K4me3, proposed to confer precise temporal activation upon differentiation. Although Polycomb repressive complex 2 is known to implement H3K27 trimethylation, the COMPASS family member responsible for H3K4me3 at bivalently marked promoters was previously unknown. Here, we identify Mll2 (KMT2b) as the enzyme catalyzing H3K4 trimethylation at bivalentlymarked promoters in embryonic stem cells. Although H3K4me3 at bivalent genes is proposed to prime future activation, we detected no substantial defect in rapid transcriptional induction after retinoic acid treatment in Mll2-depleted cells. Our identification of the Mll2 complex as the COMPASS family member responsible for H3K4me3 marking bivalent promoters provides an opportunity to reevaluate and experimentally test models for the function of bivalency in the embryonic stem cell state and in differentiation.
许多发育调控基因的启动子在胚胎干细胞状态下具有 H3K27me3 和 H3K4me3 的双价标记,据推测这种标记可以在分化时赋予精确的时间激活。尽管已知 Polycomb 抑制复合物 2 可以实现 H3K27 三甲基化,但以前不知道负责双价标记启动子上 H3K4me3 的 COMPASS 家族成员。在这里,我们鉴定出 Mll2(KMT2b)为在胚胎干细胞中催化双价标记启动子上 H3K4 三甲基化的酶。尽管双价基因上的 H3K4me3 被提议为未来激活做准备,但在 Mll2 耗尽的细胞中用视黄酸处理后,快速转录诱导并没有检测到实质性缺陷。我们鉴定出 Mll2 复合物是负责 H3K4me3 标记双价启动子的 COMPASS 家族成员,这为重新评估和实验测试胚胎干细胞状态和分化中双价的功能模型提供了机会。