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在一个GC模型中长度依赖性RNA病灶形成及重复序列相关的非AUG依赖性翻译

Length-dependent RNA foci formation and Repeat Associated non-AUG dependent translation in a G C model.

作者信息

Lamitina Todd

机构信息

Departments of Pediatrics and Cell Biology, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.

出版信息

MicroPubl Biol. 2022 Jul 15;2022. doi: 10.17912/micropub.biology.000600. eCollection 2022.

Abstract

GC-rich repeat expansion mutations are implicated in several neurodegenerative diseases and can lead to repeat associated non-AUG-dependent (RAN) translation and concentrations of nuclear RNA foci. To model ALS/FTD, we engineered to express pure GGGGCC (G C ) repeats of varying lengths and observed RAN translation and nuclear RNA foci. RNA foci were observed in animals expressing ≥20 G C repeats while RAN translation occured in animals expressing ≥33 G C repeats. These findings show that in , RAN translation can occur even in the absence of intronic sequence normally surrounding the repeat. Given that the currently accepted repeat threshold for C9 disease is >30 repeats, our data are consistent with a model in which RAN peptides are key drivers of disease pathology.

摘要

富含鸟嘌呤-胞嘧啶(GC)的重复序列扩展突变与多种神经退行性疾病有关,可导致重复序列相关的非AUG依赖(RAN)翻译以及核RNA病灶的聚集。为了模拟肌萎缩侧索硬化症/额颞叶痴呆(ALS/FTD),我们设计构建了能表达不同长度纯GGGGCC(G₄C₂)重复序列的模型,并观察到了RAN翻译和核RNA病灶。在表达≥20个G₄C₂重复序列的动物中观察到了RNA病灶,而在表达≥33个G₄C₂重复序列的动物中发生了RAN翻译。这些发现表明,在ALS/FTD中,即使没有通常围绕重复序列的内含子序列,RAN翻译也可能发生。鉴于目前公认的C9疾病重复序列阈值大于30个重复序列,我们的数据与RAN肽是疾病病理关键驱动因素的模型一致。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0abc/9315403/7277d8ab3602/25789430-2022-micropub.biology.000600.jpg

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