多谷氨酰胺(PolyQ)疾病的修饰途径:从基因筛选到药物靶点。

Marta Daniela Costa, Patrícia Maciel
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引用次数: 0

摘要

多聚谷氨酰胺(PolyQ)疾病包括一组遗传性神经退行性疾病,由特定基因编码区中 CAG 三核苷酸重复序列的不稳定扩展引起。这种基因改变会产生异常蛋白质,其中含有异常长的PolyQ束,使其更容易聚集并引起毒性。尽管近年来该领域的研究极大地促进了人们对这些疾病相关生物机制的了解,但仍然缺乏有效的治疗方法。在这篇综述中,我们重温了在多聚酶Q疾病模型(即酵母、线虫和果蝇)中所做的工作,并对利用这些系统进行的高通量无偏见遗传筛选进行了重要概述,以确定多聚酶Q疾病的新型遗传修饰因子。这些方法揭示了调节突变型 PolyQ 蛋白毒性和聚集的各种细胞过程,反映了这些疾病的复杂性,也表明了治疗策略的开发是多么具有挑战性。除了在非脊椎动物模型中进行无偏见的大规模基因筛选外,在哺乳动物系统中进行的更接近人类的补充研究也为 PolyQ 疾病提供了新的基因修饰因子,揭示了神经元功能和炎症是疾病的关键调节因子。利用多Q病遗传修饰基因的人类直向同源物进行的通路富集分析,将修饰基因聚类为可转化为人类疾病的主要主题,如蛋白质折叠和转运以及转录调控。创新的遗传操作策略,加上基因组学和生物信息学的重大进展,正在将修饰基因研究带入更现实的疾病环境中。PolyQ疾病修饰因子通路的特征描述对于揭示新的治疗方法以延缓患者疾病的发生和发展具有极其重要的意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Modifier pathways in polyglutamine (PolyQ) diseases: from genetic screens to drug targets.

Polyglutamine (PolyQ) diseases include a group of inherited neurodegenerative disorders caused by unstable expansions of CAG trinucleotide repeats in the coding region of specific genes. Such genetic alterations produce abnormal proteins containing an unusually long PolyQ tract that renders them more prone to aggregate and cause toxicity. Although research in the field in the last years has contributed significantly to the knowledge of the biological mechanisms implicated in these diseases, effective treatments are still lacking. In this review, we revisit work performed in models of PolyQ diseases, namely the yeast Saccharomyces cerevisiae, the nematode worm Caenorhabditis elegans and the fruit fly Drosophila melanogaster, and provide a critical overview of the high-throughput unbiased genetic screens that have been performed using these systems to identify novel genetic modifiers of PolyQ diseases. These approaches have revealed a wide variety of cellular processes that modulate the toxicity and aggregation of mutant PolyQ proteins, reflecting the complexity of these disorders and demonstrating how challenging the development of therapeutic strategies can be. In addition to the unbiased large-scale genetic screenings in non-vertebrate models, complementary studies in mammalian systems, closer to humans, have contributed with novel genetic modifiers of PolyQ diseases, revealing neuronal function and inflammation as key disease modulators. A pathway enrichment analysis, using the human orthologues of genetic modifiers of PolyQ diseases clustered modifier genes into major themes translatable to the human disease context, such as protein folding and transport as well as transcription regulation. Innovative genetic strategies of genetic manipulation, together with significant advances in genomics and bioinformatics, are taking modifier genetic studies to more realistic disease contexts. The characterization of PolyQ disease modifier pathways is of extreme relevance to reveal novel therapeutic possibilities to delay disease onset and progression in patients.

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来源期刊
Journal of nanoscience and nanotechnology
Journal of nanoscience and nanotechnology 工程技术-材料科学:综合
自引率
0.00%
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0
审稿时长
3.6 months
期刊介绍: JNN is a multidisciplinary peer-reviewed journal covering fundamental and applied research in all disciplines of science, engineering and medicine. JNN publishes all aspects of nanoscale science and technology dealing with materials synthesis, processing, nanofabrication, nanoprobes, spectroscopy, properties, biological systems, nanostructures, theory and computation, nanoelectronics, nano-optics, nano-mechanics, nanodevices, nanobiotechnology, nanomedicine, nanotoxicology.
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