A multimodal screening platform for endogenous dipeptide repeat proteins in C9orf72 patient iPSC neurons.

IF 7.5 1区 生物学 Q1 CELL BIOLOGY
Benedikt V Hölbling, Yashica Gupta, Paolo M Marchi, Magda L Atilano, Michael Flower, Enric Ureña, Rajkumar A Goulden, Hannah K Dobbs, Eszter Katona, Alla Mikheenko, Ashling Giblin, Ali Raza Awan, Chloe L Fisher-Ward, Niamh O'Brien, Deniz Vaizoglu, Liam Kempthorne, Katherine M Wilson, Lauren M Gittings, Mireia Carcolé, Marc-David Ruepp, Sarah Mizielinska, Linda Partridge, Pietro Fratta, Sarah J Tabrizi, Bhuvaneish T Selvaraj, Siddharthan Chandran, Emma Armstrong, Paul Whiting, Adrian M Isaacs
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引用次数: 0

Abstract

Repeat expansions in C9orf72 are the most common cause of amyotrophic lateral sclerosis and frontotemporal dementia. Repeat-associated non-AUG (RAN) translation generates neurotoxic dipeptide repeat proteins (DPRs). To study endogenous DPRs, we inserted the minimal HiBiT luciferase reporter downstream of sense repeat derived DPRs polyGA or polyGP in C9orf72 patient iPSCs. We show these "DPReporter" lines sensitively and rapidly report DPR levels in lysed and live cells and optimize screening in iPSC neurons. Small-molecule screening showed the ERK1/2 activator periplocin dose dependently increases DPR levels. Consistent with this, ERK1/2 inhibition reduced DPR levels and prolonged survival in C9orf72 repeat expansion flies. CRISPR knockout screening of all human helicases revealed telomere-associated helicases modulate DPR expression, suggesting common regulation of telomeric and C9orf72 repeats. These DPReporter lines allow investigation of DPRs in their endogenous context and provide a template for studying endogenous RAN-translated proteins, at scale, in other repeat expansion disorders.

C9orf72患者iPSC神经元内源性二肽重复蛋白的多模式筛选平台。
C9orf72重复扩张是肌萎缩性侧索硬化症和额颞叶痴呆的最常见原因。重复相关的非aug (RAN)翻译产生神经毒性二肽重复蛋白(DPRs)。为了研究内源性DPRs,我们在C9orf72患者iPSCs中插入了最小HiBiT荧光素酶报告子,该报告子位于sense repeat衍生DPRs polyGA或polyGP的下游。我们展示了这些“DPReporter”系在裂解细胞和活细胞中的敏感和快速报告DPR水平,并优化了在iPSC神经元中的筛选。小分子筛选显示ERK1/2激活剂periplocin剂量依赖性地增加DPR水平。与此一致的是,ERK1/2抑制降低了DPR水平,延长了C9orf72重复扩增蝇的存活时间。对所有人类解旋酶进行CRISPR敲除筛选,发现端粒相关解旋酶可调节DPR表达,提示端粒和C9orf72重复序列的共同调控。这些DPReporter系允许在内源性环境中研究DPRs,并为大规模研究其他重复扩增疾病中的内源性ran翻译蛋白提供模板。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Cell reports
Cell reports CELL BIOLOGY-
CiteScore
13.80
自引率
1.10%
发文量
1305
审稿时长
77 days
期刊介绍: Cell Reports publishes high-quality research across the life sciences and focuses on new biological insight as its primary criterion for publication. The journal offers three primary article types: Reports, which are shorter single-point articles, research articles, which are longer and provide deeper mechanistic insights, and resources, which highlight significant technical advances or major informational datasets that contribute to biological advances. Reviews covering recent literature in emerging and active fields are also accepted. The Cell Reports Portfolio includes gold open-access journals that cover life, medical, and physical sciences, and its mission is to make cutting-edge research and methodologies available to a wide readership. The journal's professional in-house editors work closely with authors, reviewers, and the scientific advisory board, which consists of current and future leaders in their respective fields. The advisory board guides the scope, content, and quality of the journal, but editorial decisions are independently made by the in-house scientific editors of Cell Reports.
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