Department of Pathology, University of Michigan Medical School, Ann Arbor, Michigan; Rogel Cancer Center, University of Michigan, Ann Arbor, Michigan; Department of Internal Medicine, University of Michigan Medical School, Ann Arbor, Michigan.
Department of Pathology, University of Michigan Medical School, Ann Arbor, Michigan; Rogel Cancer Center, University of Michigan, Ann Arbor, Michigan.
Am J Pathol. 2021 May;191(5):774-783. doi: 10.1016/j.ajpath.2021.01.013. Epub 2021 Feb 6.
Enhancer of Zeste Homologue 2 (EZH2) is the catalytic subunit of the polycomb repressive complex 2 (PRC2) that is critical for determining cell identity. An epigenetic writer, EZH2 has a well-defined role in transcriptional repression by depositing trimethyl marks on lysine 27 of histone H3. However, there is mounting evidence that histone methyltransferases like EZH2 exert histone methyltransferase-independent functions. The relevance of these functions to breast cancer progression and their regulatory mechanisms are only beginning to become understood. Here, we review the current understanding of EZH2 H3K27me3-independent, noncanonical, functions and their regulation in breast cancer.
增强子结合锌指蛋白 2(EZH2)是多梳抑制复合物 2(PRC2)的催化亚基,对于确定细胞身份至关重要。EZH2 作为一种表观遗传写入器,通过在组蛋白 H3 的赖氨酸 27 上沉积三甲基标记,在转录抑制中发挥着明确的作用。然而,越来越多的证据表明,EZH2 等组蛋白甲基转移酶发挥着组蛋白甲基转移酶非依赖性的功能。这些功能与乳腺癌进展的相关性及其调控机制才刚刚开始被理解。在这里,我们综述了目前对 EZH2 H3K27me3 非依赖性、非典型功能及其在乳腺癌中的调控的认识。