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多样化的异染色质状态限制细胞身份和重编程。

Diverse heterochromatin states restricting cell identity and reprogramming.

机构信息

Institute for Regenerative Medicine, Penn Epigenetics Institute, Department of Cell and Developmental Biology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.

Institute for Regenerative Medicine, Penn Epigenetics Institute, Department of Cell and Developmental Biology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.

出版信息

Trends Biochem Sci. 2023 Jun;48(6):513-526. doi: 10.1016/j.tibs.2023.02.007. Epub 2023 Mar 27.

Abstract

Heterochromatin is defined as a chromosomal domain harboring repressive H3K9me2/3 or H3K27me3 histone modifications and relevant factors that physically compact the chromatin. Heterochromatin can restrict where transcription factors bind, providing a barrier to gene activation and changes in cell identity. While heterochromatin thus helps maintain cell differentiation, it presents a barrier to overcome during efforts to reprogram cells for biomedical purposes. Recent findings have revealed complexity in the composition and regulation of heterochromatin, and shown that transiently disrupting the machinery of heterochromatin can enhance reprogramming. Here, we discuss how heterochromatin is established and maintained during development, and how our growing understanding of the mechanisms regulating H3K9me3 heterochromatin can be leveraged to improve our ability to direct changes in cell identity.

摘要

异染色质被定义为含有抑制性 H3K9me2/3 或 H3K27me3 组蛋白修饰和相关因子的染色体结构域,这些因子可使染色质物理性紧缩。异染色质可以限制转录因子的结合位置,为基因激活和细胞身份的改变提供障碍。虽然异染色质有助于维持细胞分化,但在为生物医学目的重新编程细胞时,它是需要克服的障碍。最近的研究结果揭示了异染色质组成和调控的复杂性,并表明暂时破坏异染色质的机制可以增强重编程。在这里,我们讨论了异染色质在发育过程中是如何建立和维持的,以及我们对调控 H3K9me3 异染色质的机制的理解如何被用来提高我们改变细胞身份的能力。

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