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BAP1 复合物通过拮抗 PRC1 介导的 H2A 泛素化促进转录。

BAP1 complex promotes transcription by opposing PRC1-mediated H2A ubiquitylation.

机构信息

Institut Curie, Paris Sciences et Lettres Research University, Sorbonne University, 75005, Paris, France.

INSERM U934/CNRS UMR3215, 75005, Paris, France.

出版信息

Nat Commun. 2019 Jan 21;10(1):348. doi: 10.1038/s41467-018-08255-x.

Abstract

In Drosophila, a complex consisting of Calypso and ASX catalyzes H2A deubiquitination and has been reported to act as part of the Polycomb machinery in transcriptional silencing. The mammalian homologs of these proteins (BAP1 and ASXL1/2/3, respectively), are frequently mutated in various cancer types, yet their precise functions remain unclear. Using an integrative approach based on isogenic cell lines generated with CRISPR/Cas9, we uncover an unanticipated role for BAP1 in gene activation. This function requires the assembly of an enzymatically active BAP1-associated core complex (BAP1.com) containing one of the redundant ASXL proteins. We investigate the mechanism underlying BAP1.com-mediated transcriptional regulation and show that it does not participate in Polycomb-mediated silencing. Instead, our results establish that the function of BAP1.com is to safeguard transcriptionally active genes against silencing by the Polycomb Repressive Complex 1.

摘要

在果蝇中,由 Calypso 和 ASX 组成的复合物催化 H2A 的去泛素化,并且已被报道作为转录沉默的 Polycomb 机制的一部分。这些蛋白质的哺乳动物同源物(分别为 BAP1 和 ASXL1/2/3)在各种癌症类型中经常发生突变,但它们的确切功能仍不清楚。我们使用基于 CRISPR/Cas9 生成的同源细胞系的综合方法,揭示了 BAP1 在基因激活中的一个意外作用。该功能需要组装具有酶活性的 BAP1 相关核心复合物(BAP1.com),其中包含一个冗余的 ASXL 蛋白。我们研究了 BAP1.com 介导的转录调控的机制,并表明它不参与 Polycomb 介导的沉默。相反,我们的结果表明,BAP1.com 的功能是保护转录活跃的基因免受 Polycomb 抑制复合物 1 的沉默。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab51/6341105/56d9cd648812/41467_2018_8255_Fig1_HTML.jpg

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