Cell Biosci. 2013 Oct 9;3(1):39. doi: 10.1186/2045-3701-3-39.
Epigenetic mechanisms are fundamental to understanding the regulatory networks of gene expression that govern stem cell maintenance and differentiation. Methylated histone H3 lysine 4 (H3K4) has emerged as a key epigenetic signal for gene transcription; it is dynamically modulated by several specific H3K4 methyltransferases and demethylases. Recent studies have described new epigenetic mechanisms by which H3K4 methylation modifiers control self-renewal and lineage commitments of stem cells. Such advances in stem cell biology would have a high impact on the research fields of cancer stem cell and regenerative medicine. In this review, we discuss the recent progress in understanding the roles of H3K4 methylation modifiers in regulating embryonic and adult stem cells' fates.
表观遗传机制对于理解调控干细胞维持和分化的基因表达调控网络至关重要。组蛋白 H3 赖氨酸 4 甲基化 (H3K4) 已成为基因转录的关键表观遗传信号;它被几种特定的 H3K4 甲基转移酶和去甲基酶动态调节。最近的研究描述了 H3K4 甲基化修饰因子控制干细胞自我更新和谱系决定的新表观遗传机制。这些在干细胞生物学方面的进展将对癌症干细胞和再生医学等研究领域产生重大影响。在这篇综述中,我们讨论了目前对 H3K4 甲基化修饰因子在调节胚胎和成人干细胞命运中的作用的理解进展。