Department of Medicine, University of Pittsburgh School of Medicine, Pittsburgh, PA, 15213, USA.
Department of Pathology, University of Pittsburgh School of Medicine, Pittsburgh, PA, 15213, USA.
Nat Commun. 2024 Jun 17;15(1):5155. doi: 10.1038/s41467-024-49486-5.
Dysregulated epigenetic states are a hallmark of cancer and often arise from genetic alterations in epigenetic regulators. This includes missense mutations in histones, which, together with associated DNA, form nucleosome core particles. However, the oncogenic mechanisms of most histone mutations are unknown. Here, we demonstrate that cancer-associated histone mutations at arginines in the histone H3 N-terminal tail disrupt repressive chromatin domains, alter gene regulation, and dysregulate differentiation. We find that histone H3R2C and R26C mutants reduce transcriptionally repressive H3K27me3. While H3K27me3 depletion in cells expressing these mutants is exclusively observed on the minor fraction of histone tails harboring the mutations, the same mutants recurrently disrupt broad H3K27me3 domains in the chromatin context, including near developmentally regulated promoters. H3K27me3 loss leads to de-repression of differentiation pathways, with concordant effects between H3R2 and H3R26 mutants despite different proximity to the PRC2 substrate, H3K27. Functionally, H3R26C-expressing mesenchymal progenitor cells and murine embryonic stem cell-derived teratomas demonstrate impaired differentiation. Collectively, these data show that cancer-associated H3 N-terminal arginine mutations reduce PRC2 activity and disrupt chromatin-dependent developmental functions, a cancer-relevant phenotype.
表观遗传状态失调是癌症的一个标志,通常源于表观遗传调控因子的遗传改变。这包括组蛋白中的错义突变,组蛋白与相关的 DNA 一起形成核小体核心颗粒。然而,大多数组蛋白突变的致癌机制尚不清楚。在这里,我们证明了组蛋白 H3 N 端尾部的致癌相关精氨酸突变破坏了抑制性染色质域,改变了基因调控,并扰乱了分化。我们发现,组蛋白 H3R2C 和 R26C 突变体降低了转录抑制性 H3K27me3。虽然在表达这些突变体的细胞中观察到 H3K27me3 的耗竭仅发生在携带突变的组蛋白尾部的次要部分上,但相同的突变体在染色质背景中频繁破坏广泛的 H3K27me3 域,包括发育调控的启动子附近。H3K27me3 的丢失导致分化途径去抑制,尽管 H3R2 和 H3R26 突变体与 PRC2 底物 H3K27 的接近程度不同,但在 H3R2 和 H3R26 突变体之间存在一致的效应。功能上,表达 H3R26C 的间充质祖细胞和源自小鼠胚胎干细胞的畸胎瘤显示出分化受损。总的来说,这些数据表明,与癌症相关的 H3 N 端精氨酸突变降低了 PRC2 的活性,并破坏了依赖染色质的发育功能,这是一种与癌症相关的表型。