Caputo Anthony, Schaffer Ashleigh E
Department of Genetics and Genome Sciences, Case Western Reserve University School of Medicine, Cleveland, Ohio, United States.
Department of Genetics and Genome Sciences, Case Western Reserve University School of Medicine, Cleveland, Ohio, United States.
Curr Opin Genet Dev. 2025 Apr;91:102322. doi: 10.1016/j.gde.2025.102322. Epub 2025 Feb 8.
Intellectual disability (ID) is a broad diagnostic category that encompasses individuals with impaired cognitive ability. While these disorders have heterogeneous causes, recent developments in next-generation sequencing (NGS) are revealing the prevalence of genetic etiologies. In particular, germline mutations in genes that affect RNA splicing are increasingly common causes of ID disorders. Research to elucidate the functional relationship between splicing and neurodevelopment is critical since molecular therapeutics require a nuanced understanding of the pathological mechanism. In this review, we first summarize the trends that have led to the discovery of the RNA splicing-ID relationship, then discuss recent progress and future directions for research surrounding RNA splicing in neurodevelopment. Finally, we speak on how these results may serve as the foundation for burgeoning therapies.
智力障碍(ID)是一个广泛的诊断类别,涵盖认知能力受损的个体。虽然这些疾病的病因多种多样,但下一代测序(NGS)的最新进展正在揭示遗传病因的普遍性。特别是,影响RNA剪接的基因中的种系突变越来越成为ID疾病的常见病因。阐明剪接与神经发育之间的功能关系的研究至关重要,因为分子疗法需要对病理机制有细致入微的理解。在这篇综述中,我们首先总结了导致发现RNA剪接与ID关系的趋势,然后讨论了围绕神经发育中RNA剪接的研究的最新进展和未来方向。最后,我们谈谈这些结果如何可能成为新兴疗法的基础。