Key Laboratory of Biorheological Science and Technology, Ministry of Education, College of Bioengineering, Chongqing University, Chongqing 400044, China.
Gene. 2013 Oct 1;528(1):21-6. doi: 10.1016/j.gene.2013.06.027. Epub 2013 Jun 23.
The main function of skeletal system is to support the body and help movement. A variety of factors can lead to skeletal system disease, including age, exercise, and of course genetic makeup and expression. Pre-mRNA splicing plays a crucial role in gene expression, by creating multiple protein variants with different biological functions. The recent studies show that several skeletal system diseases are related to pre-mRNA splicing. This review focuses on the relationship between pre-mRNA splicing and skeletal system disease. On the one hand, splice site mutation that leads to aberrant splicing often causes genetic skeletal system disease, like COL1A1, SEDL and LRP5. On the other hand, alternative splicing without genomic mutation may generate some marker protein isoforms, for example, FN, VEGF and CD44. Therefore, understanding the relationship between pre-mRNA splicing and skeletal system disease will aid in uncovering the mechanism of disease and contribute to the future development of gene therapy.
骨骼系统的主要功能是支撑身体并帮助运动。多种因素可导致骨骼系统疾病,包括年龄、运动,当然还有遗传组成和表达。前体 mRNA 剪接在基因表达中起着至关重要的作用,它通过创建具有不同生物学功能的多种蛋白质变体来实现。最近的研究表明,几种骨骼系统疾病与前体 mRNA 剪接有关。本综述重点关注前体 mRNA 剪接与骨骼系统疾病之间的关系。一方面,导致异常剪接的剪接位点突变常引起遗传性骨骼系统疾病,如 COL1A1、SEDL 和 LRP5。另一方面,没有基因组突变的选择性剪接可能会产生一些标记蛋白同工型,例如 FN、VEGF 和 CD44。因此,了解前体 mRNA 剪接与骨骼系统疾病之间的关系将有助于揭示疾病的机制,并为未来的基因治疗发展做出贡献。