Department of Medical Biotechnology, Institute of Bioorganic Chemistry Polish Academy of Sciences, 61-704 Poznań, Poland.
Cells. 2022 Feb 15;11(4):677. doi: 10.3390/cells11040677.
Repeat expansion diseases are a group of more than 40 disorders that affect mainly the nervous and/or muscular system and include myotonic dystrophies, Huntington's disease, and fragile X syndrome. The mutation-driven expanded repeat tract occurs in specific genes and is composed of tri- to dodeca-nucleotide-long units. Mutant mRNA is a pathogenic factor or important contributor to the disease and has great potential as a therapeutic target. Although repeat expansion diseases are quite well known, there are limited studies concerning polyadenylation events for implicated transcripts that could have profound effects on transcript stability, localization, and translation efficiency. In this review, we briefly present polyadenylation and alternative polyadenylation (APA) mechanisms and discuss their role in the pathogenesis of selected diseases. We also discuss several methods for poly(A) tail measurement (both transcript-specific and transcriptome-wide analyses) and APA site identification-the further development and use of which may contribute to a better understanding of the correlation between APA events and repeat expansion diseases. Finally, we point out some future perspectives on the research into repeat expansion diseases, as well as APA studies.
重复扩展疾病是一组超过 40 种疾病,主要影响神经系统和/或肌肉系统,包括肌强直性营养不良、亨廷顿病和脆性 X 综合征。突变驱动的扩展重复片段发生在特定基因中,由三到十二核苷酸长的单元组成。突变的 mRNA 是疾病的致病因素或重要贡献者,具有作为治疗靶点的巨大潜力。尽管重复扩展疾病已经相当为人所知,但关于涉及的转录物的聚腺苷酸化事件的研究有限,这些事件可能对转录本的稳定性、定位和翻译效率产生深远影响。在这篇综述中,我们简要介绍了聚腺苷酸化和可变聚腺苷酸化(APA)机制,并讨论了它们在选定疾病发病机制中的作用。我们还讨论了几种聚(A)尾测量方法(转录特异性和转录组范围分析)和 APA 位点鉴定——进一步开发和使用这些方法可能有助于更好地理解 APA 事件与重复扩展疾病之间的相关性。最后,我们指出了重复扩展疾病以及 APA 研究的一些未来研究方向。