参与板层相关结构域基因抑制的染色质蛋白复合物

IF 9.4 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY EMBO Journal Pub Date : 2024-11-01 Epub Date: 2024-09-25 DOI:10.1038/s44318-024-00214-1
Stefano G Manzo, Abdelghani Mazouzi, Christ Leemans, Tom van Schaik, Nadia Neyazi, Marjon S van Ruiten, Benjamin D Rowland, Thijn R Brummelkamp, Bas van Steensel
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引用次数: 0

摘要

核薄层相关域(LAD)是与核薄层(NL)相关的大型染色质区域,形成了抑制转录的环境。目前,LADs 中介导基因抑制的分子角色尚不清楚。在这里,我们使用 LAD 整合荧光报告物对人类细胞进行了基于 FACS 的全基因组遗传筛选,以确定此类调控因子。令人惊讶的是,筛选结果发现的 NL 蛋白很少,但却揭示了数十种已知染色质调控因子的作用。其中包括负伸长因子(NELF)复合物和参与 RNA 聚合酶暂停的相互作用因子,这表明转录伸长的调控是 LADs 中抑制转录的一种机制。此外,染色质重塑复合物 BAF 和激活复合物 Mediator 在 LADs 中既可作为激活因子,也可作为抑制因子,这取决于局部环境,也可能是通过重新连接异染色质来实现的。我们的数据表明,转录和染色质重塑的基本调节因子,而不是与 NL 蛋白的相互作用,在 LADs 内的转录调节中发挥着重要作用。
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Chromatin protein complexes involved in gene repression in lamina-associated domains.

Lamina-associated domains (LADs) are large chromatin regions that are associated with the nuclear lamina (NL) and form a repressive environment for transcription. The molecular players that mediate gene repression in LADs are currently unknown. Here, we performed FACS-based whole-genome genetic screens in human cells using LAD-integrated fluorescent reporters to identify such regulators. Surprisingly, the screen identified very few NL proteins, but revealed roles for dozens of known chromatin regulators. Among these are the negative elongation factor (NELF) complex and interacting factors involved in RNA polymerase pausing, suggesting that regulation of transcription elongation is a mechanism to repress transcription in LADs. Furthermore, the chromatin remodeler complex BAF and the activation complex Mediator can work both as activators and repressors in LADs, depending on the local context and possibly by rewiring heterochromatin. Our data indicate that the fundamental regulators of transcription and chromatin remodeling, rather than interaction with NL proteins, play a major role in transcription regulation within LADs.

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来源期刊
EMBO Journal
EMBO Journal 生物-生化与分子生物学
CiteScore
18.90
自引率
0.90%
发文量
246
审稿时长
1.5 months
期刊介绍: The EMBO Journal has stood as EMBO's flagship publication since its inception in 1982. Renowned for its international reputation in quality and originality, the journal spans all facets of molecular biology. It serves as a platform for papers elucidating original research of broad general interest in molecular and cell biology, with a distinct focus on molecular mechanisms and physiological relevance. With a commitment to promoting articles reporting novel findings of broad biological significance, The EMBO Journal stands as a key contributor to advancing the field of molecular biology.
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