School of Medicine, Life and Health Sciences Research Institute (ICVS), University of Minho, 4710-057, Braga, Portugal.
ICVS/3Bs-PT Government Associate Laboratory, Braga/Guimarães, Portugal.
Cell Mol Life Sci. 2022 May 3;79(5):274. doi: 10.1007/s00018-022-04280-8.
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.
多聚谷氨酰胺(PolyQ)疾病包括一组遗传性神经退行性疾病,其病因是特定基因编码区中 CAG 三核苷酸重复不稳定扩展。这种遗传改变产生了含有异常长的 PolyQ 片段的异常蛋白质,使它们更容易聚集并产生毒性。尽管近年来该领域的研究对这些疾病所涉及的生物学机制有了重大贡献,但仍缺乏有效的治疗方法。在这篇综述中,我们重新审视了 PolyQ 疾病模型中的工作,即酵母酿酒酵母、线虫秀丽隐杆线虫和果蝇黑腹果蝇,并对使用这些系统进行的高通量无偏遗传筛选进行了批判性概述,以鉴定 PolyQ 疾病的新的遗传修饰因子。这些方法揭示了多种调节突变型 PolyQ 蛋白毒性和聚集的细胞过程,反映了这些疾病的复杂性,并表明开发治疗策略的挑战性有多大。除了在非脊椎动物模型中进行无偏的大规模遗传筛选外,与人类更接近的哺乳动物系统中的互补研究也为 PolyQ 疾病的新遗传修饰因子做出了贡献,揭示了神经元功能和炎症是关键的疾病调节剂。使用 PolyQ 疾病遗传修饰因子的人类同源物进行通路富集分析,将修饰基因聚类到可转化为人类疾病背景的主要主题中,例如蛋白质折叠和运输以及转录调控。遗传操作的创新遗传策略,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推向更现实的疾病背景。PolyQ 疾病修饰途径的特征对于揭示新的治疗可能性以延迟患者疾病的发作和进展至关重要。