发育和癌症中多聚核苷酸指导的细胞命运决定。

IF 2.5 Q3 GENETICS & HEREDITY
Beatriz German, Leigh Ellis
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引用次数: 0

摘要

多聚核糖体(PcG)蛋白是整个进化过程中高度保守的转录调控子集。它们的主要作用是对染色质景观进行表观遗传修饰,控制主转录程序的表达,从而决定细胞的特性。迄今为止,在哺乳动物中发现的两个主要 PcG 蛋白复合物是多聚核抑制复合体 1(PRC1)和 2(PRC2)。这些蛋白复合物通过诱导共价翻译后组蛋白修饰,促进染色质结构稳定,从而选择性地抑制基因表达。PRC2 催化组蛋白 H3 在赖氨酸 27 处的甲基化(H3K27me1/2/3),诱导异染色质结构。这一活性受控于一个多亚基复合物的形成,该复合物包括泽斯特增强子(EZH2)、胚胎外胚层发育蛋白(EED)和泽斯特12抑制因子(SUZ12)。本综述将总结有关哺乳动物细胞中 PRC2 如何调控转录以协调基因的时间性和组织特异性表达从而决定细胞身份和细胞命运的最新见解。我们将具体描述不同细胞类型中 PRC2 的失调如何促进表型可塑性和/或非突变性表观遗传重编程,诱发侵袭性极强的上皮神经内分泌癌,包括前列腺癌、小细胞肺癌和梅克尔细胞癌。因此,EZH2 已成为此类癌症的重要治疗靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Polycomb Directed Cell Fate Decisions in Development and Cancer.

Polycomb Directed Cell Fate Decisions in Development and Cancer.

Polycomb Directed Cell Fate Decisions in Development and Cancer.

Polycomb Directed Cell Fate Decisions in Development and Cancer.

The polycomb group (PcG) proteins are a subset of transcription regulators highly conserved throughout evolution. Their principal role is to epigenetically modify chromatin landscapes and control the expression of master transcriptional programs to determine cellular identity. The two mayor PcG protein complexes that have been identified in mammals to date are Polycomb Repressive Complex 1 (PRC1) and 2 (PRC2). These protein complexes selectively repress gene expression via the induction of covalent post-translational histone modifications, promoting chromatin structure stabilization. PRC2 catalyzes the histone H3 methylation at lysine 27 (H3K27me1/2/3), inducing heterochromatin structures. This activity is controlled by the formation of a multi-subunit complex, which includes enhancer of zeste (EZH2), embryonic ectoderm development protein (EED), and suppressor of zeste 12 (SUZ12). This review will summarize the latest insights into how PRC2 in mammalian cells regulates transcription to orchestrate the temporal and tissue-specific expression of genes to determine cell identity and cell-fate decisions. We will specifically describe how PRC2 dysregulation in different cell types can promote phenotypic plasticity and/or non-mutational epigenetic reprogramming, inducing the development of highly aggressive epithelial neuroendocrine carcinomas, including prostate, small cell lung, and Merkel cell cancer. With this, EZH2 has emerged as an important actionable therapeutic target in such cancers.

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来源期刊
Epigenomes
Epigenomes GENETICS & HEREDITY-
CiteScore
3.80
自引率
0.00%
发文量
38
审稿时长
11 weeks
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