用基因编辑技术解决面岬肱肌营养不良症。

IF 4.9 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Frontiers in genome editing Pub Date : 2022-07-15 eCollection Date: 2022-01-01 DOI:10.3389/fgeed.2022.937879
Virginie Mariot, Julie Dumonceaux
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引用次数: 0

摘要

面岬肱肌营养不良症(FSHD)是一种骨骼肌疾病,由肌肉组织中 DUX4 基因的异常表达引起。迄今为止,针对 DNA、RNA 或蛋白质水平上的 DUX4 提出了不同的治疗方法。最近,基于簇状规则间距短基因重复(CRISPR)技术的发展开辟了新的研究途径,前列腺肥大症也不例外。遗传性肌肉疾病首次有了治愈的可能。在此,我们将介绍目前正在研究的基于CRISPR的FSHD治疗策略。不同的方法包括针对 DUX4 基因及其启动子的表观基因组编辑,使用 TALEN、CRISPR/cas9 或腺嘌呤碱基编辑针对 DUX4 多腺苷酸化的基因编辑,以及针对 SMCHD1 的 CRISPR-Cas9 基因组编辑。我们还讨论了开发这些基于基因编辑的疗法所面临的挑战。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Gene Editing to Tackle Facioscapulohumeral Muscular Dystrophy.

Gene Editing to Tackle Facioscapulohumeral Muscular Dystrophy.

Gene Editing to Tackle Facioscapulohumeral Muscular Dystrophy.

Gene Editing to Tackle Facioscapulohumeral Muscular Dystrophy.

Facioscapulohumeral dystrophy (FSHD) is a skeletal muscle disease caused by the aberrant expression of the DUX4 gene in the muscle tissue. To date, different therapeutic approaches have been proposed, targeting DUX4 at the DNA, RNA or protein levels. The recent development of the clustered regularly interspaced short-palindromic repeat (CRISPR) based technology opened new avenues of research, and FSHD is no exception. For the first time, a cure for genetic muscular diseases can be considered. Here, we describe CRISPR-based strategies that are currently being investigated for FSHD. The different approaches include the epigenome editing targeting the DUX4 gene and its promoter, gene editing targeting the polyadenylation of DUX4 using TALEN, CRISPR/cas9 or adenine base editing and the CRISPR-Cas9 genome editing for SMCHD1. We also discuss challenges facing the development of these gene editing based therapeutics.

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来源期刊
CiteScore
7.00
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