| Literature DB >> 30171557 |
Natalia N Singh1, Diou Luo2, Ravindra N Singh2.
Abstract
Pre-mRNA splicing, a dynamic process of intron removal and exon joining, is governed by a combinatorial control exerted by overlapping cis-elements that are unique to each exon and its flanking intronic sequences. Splicing cis-elements are usually 4-to-8-nucleotide-long linear motifs that provide binding sites for specific proteins. Pre-mRNA splicing is also influenced by secondary and higher order RNA structures that affect accessibility of splicing cis-elements. Antisense oligonucleotides (ASOs) that block splicing cis-elements and/or affect RNA structure have been shown to modulate splicing in vivo. Therefore, ASO-based strategies have emerged as a powerful tool for therapeutic manipulation of splicing in pathological conditions. Here we describe an ASO-based approach to increase the production of the full-length SMN2 mRNA in spinal muscular atrophy patient cells.Entities:
Keywords: 2′-O-methyl modification; Antisense oligonucleotide (ASO); Intronic splicing silencer N1 (ISS-N1); Nucleofection; Phosphoroamidate morpholino oligonucleotide (PMO); Phosphorothioate backbone; Pre-mRNA splicing; Spinal muscular atrophy (SMA); Survival motor neuron (SMN); Transfection
Mesh:
Substances:
Year: 2018 PMID: 30171557 PMCID: PMC6195309 DOI: 10.1007/978-1-4939-8651-4_26
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745