Addressing the Tissue Specificity of U5 snRNP Spliceosomopathies

Rahmat Azhari Kemal ^1,2 Raymond Thomas O'Keefe ^1*

• ¹ The University of Manchester, Manchester, England, United Kingdom
• ² Universitas Riau, Pekanbaru, Indonesia

Precursor mRNA (pre-mRNA) must undergo splicing to remove intron sequences and join exons. This splicing process is catalysed by an RNA/protein complex called the spliceosome. At the centre of the catalytic spliceosome is the U5 small nuclear ribonucleoprotein (snRNP). Mutations in U5 snRNP core proteins are associated with various diseases commonly known as spliceosomopathies. Mutations in TXNL4A and EFTUD2 manifest in craniofacial malformations while mutations in PRPF8 and SNRNP200 manifest in retinitis pigmentosa. This perspective highlights research addressing how these specific manifestations come about as the spliceosome is required in all cells and at all developmental stages. Cell and animal models can replicate the human clinical specificity providing explanations for the specificity of the disorders. We propose that future research could benefit from models originating from patient-derived induced pluripotent stem cells (iPSCs) and isogenic controls to compare the coding and non-coding transcriptomic perturbations. Analysis of spliceosomal protein complexes and their interactome could also uncover novel insights on molecular pathogenesis. Finally, as studies highlight changes in metabolic processes, metabolomic studies could become a new venture in studying the consequences of U5 snRNP mutations.