Differential fates of introns in gene expression due to global alternative splicing

Kumari, Anjani; Sedehizadeh, Saam; Brook, John David; Kozlowski, Piotr; Wojciechowska, Marzena

Abstract

The discovery of introns over four decades ago revealed a new vision of genes and their interrupted arrangement. Throughout the years, it has appeared that introns play essential roles in the regulation of gene expression. Unique processing of excised introns through the formation of lariats suggests a widespread role for these molecules in the structure and function of cells. In addition to rapid destruction, these lariats may linger on in the nucleus or may even be exported to the cytoplasm, where they remain stable circular RNAs (circRNAs). Alternative splicing (AS) is a source of diversity in mature transcripts harboring retained introns (RI-mRNAs). Such RNAs may contain one or more entire retained intron(s) (RIs), but they may also have intron fragments resulting from sequential excision of smaller subfragments via recursive splicing (RS), which is characteristic of long introns. There are many potential fates of RI-mRNAs, including their downregulation via nuclear and cytoplasmic surveillance systems and the generation of new protein isoforms with potentially different functions. Various reports have linked the presence of such unprocessed transcripts in mammals to important roles in normal development and in disease-related conditions. In certain human neurological-neuromuscular disorders, including myotonic dystrophy type 2 (DM2), frontotemporal dementia/amyotrophic lateral sclerosis (FTD/ALS) and Duchenne muscular dystrophy (DMD), peculiar processing of long introns has been identified and is associated with their pathogenic effects. In this review, we discuss different mechanisms involved in the processing of introns during AS and the functions of these large sections of the genome in our biology.

Citation

Kumari, A., Sedehizadeh, S., Brook, J. D., Kozlowski, P., & Wojciechowska, M. (2022). Differential fates of introns in gene expression due to global alternative splicing. Human Genetics, 141, 31-47. https://doi.org/10.1007/s00439-021-02409-6

• Journal Article Type: Article
• Acceptance Date: Dec 2, 2021
• Online Publication Date: Dec 14, 2021
• Publication Date: 2022-01
• Deposit Date: Mar 6, 2025
• Publicly Available Date: Mar 6, 2025
• Journal: Human Genetics
• Print ISSN: 0340-6717
• Electronic ISSN: 1432-1203
• Publisher: Springer Verlag
• Peer Reviewed: Peer Reviewed
• Volume: 141
• Pages: 31-47
• DOI: https://doi.org/10.1007/s00439-021-02409-6
• Public URL: https://nottingham-repository.worktribe.com/output/46191908
• Publisher URL: https://link.springer.com/article/10.1007/s00439-021-02409-6
• Additional Information: Received: 8 August 2021; Accepted: 2 December 2021; First Online: 14 December 2021; : ; : The authors declare no conflict of interest.; : Not applicable.; : Not applicable.; : Not applicable.