多维组学揭示了ARID1A在正常样和恶性尿路上皮细胞中对DNA损伤、剪接和细胞周期的精心控制。

IF 6.6 2区 医学 Q1 Biochemistry, Genetics and Molecular Biology
Rebecca M Schlösser, Florian Krumbach, Eyleen Corrales, Geoffroy Andrieux, Christian Preisinger, Franziska Liss, Alexandra Golzmann, Melanie Boerries, Kerstin Becker, Ruth Knüchel, Stefan Garczyk, Bernhard Lüscher
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引用次数: 0

摘要

表观遗传调控因子,如SWI/SNF复合物,在组织发育和体内平衡中起重要作用,在癌症中经常发生突变。ARID1A是SWI/SNF复合体的一个亚基,在大约20%的膀胱肿瘤中发生突变;然而,人们对其后果仍知之甚少。发现截断是最常见的突变,我们建立了功能丧失和功能获得模型,进行RNA-Seq、相互作用组分析、Omni-ATAC-Seq和功能研究,以表征可能适合治疗arid1a缺陷膀胱癌的arid1a影响通路。我们观察到,在arid1a缺陷细胞中,细胞增殖减少,包括DNA修复在内的应激调节通路解除管制。此外,ARID1A与RNA和相互作用组水平上的选择性剪接和翻译调控有关。在功能富集分析中,ARID1A缺陷极大地降低了染色质的可及性,特别是在内含子和远端增强子周围。不易接近的染色质区域被映射到细胞增殖和DNA损伤反应等途径。事实上,在arid1a缺陷细胞中,DNA损伤后G2/M检查点出现受损。总之,我们的数据强调了ARID1A缺失的广泛影响以及靶向增殖和DNA修复途径进行治疗的可能性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Multidimensional OMICs reveal ARID1A orchestrated control of DNA damage, splicing, and cell cycle in normal-like and malignant urothelial cells.

Epigenetic regulators, such as the SWI/SNF complex, with important roles in tissue development and homeostasis, are frequently mutated in cancer. ARID1A, a subunit of the SWI/SNF complex, is mutated in approximately 20% of all bladder tumors; however, the consequences of this remain poorly understood. Finding truncations to be the most common mutation, we generated loss- and gain-of-function models to conduct RNA-Seq, interactome analyses, Omni-ATAC-Seq, and functional studies to characterize ARID1A-affected pathways potentially suitable for the treatment of ARID1A-deficient bladder cancers. We observed decreased cell proliferation and deregulation of stress-regulated pathways, including DNA repair, in ARID1A-deficient cells. Furthermore, ARID1A was linked to alternative splicing and translational regulation on RNA and interactome levels. ARID1A deficiency drastically reduced the accessibility of chromatin, especially around introns and distal enhancers, in a functional enrichment analysis. Less accessible chromatin areas were mapped to pathways such as cell proliferation and DNA damage response. Indeed, the G2/M checkpoint appeared impaired after DNA damage in ARID1A-deficient cells. Together, our data highlight the broad impact of ARID1A loss and the possibility of targeting proliferative and DNA repair pathways for treatment.

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来源期刊
Molecular Oncology
Molecular Oncology Biochemistry, Genetics and Molecular Biology-Molecular Medicine
CiteScore
11.80
自引率
1.50%
发文量
203
审稿时长
10 weeks
期刊介绍: Molecular Oncology highlights new discoveries, approaches, and technical developments, in basic, clinical and discovery-driven translational cancer research. It publishes research articles, reviews (by invitation only), and timely science policy articles. The journal is now fully Open Access with all articles published over the past 10 years freely available.
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