期刊
RNA
卷 16, 期 6, 页码 1167-1181出版社
COLD SPRING HARBOR LAB PRESS, PUBLICATIONS DEPT
DOI: 10.1261/rna.2154310
关键词
SMN; alternative splicing; intron 7; exon 7; ISS-N1; GC-rich; antisense oligonucleotide; ASO; SMA
资金
- United States National Institutes of Health [R01NS055925]
- Salsbury Endowment at Iowa State University
- Center for Integrated Animal Genomics at Iowa State University
- Iowa Center for Advanced Neurotoxicology
- NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE [R01NS055925] Funding Source: NIH RePORTER
Here we report a novel finding of an antisense oligonucleotide (ASO) microwalk in which we examined the position-specific role of intronic residues downstream from the 5' splice site (5' ss) of SMN2 exon 7, skipping of which is associated with spinal muscular atrophy (SMA), a leading genetic cause of infant mortality. Our results revealed the inhibitory role of a cytosine residue at the 10th intronic position (C-10), which is neither conserved nor associated with any known splicing motif. Significance of C-10 emerged from the splicing pattern of SMN2 exon 7 in presence of a 14-mer ASO (L14) that sequestered two adjacent hnRNP A1 motifs downstream from C-10 and yet promoted SMN2 exon 7 skipping. Another 14-mer ASO (F14) that sequestered both, C-10 and adjacent hnRNP A1 motifs, led to a strong stimulation of SMN2 exon 7 inclusion. The inhibitory role of C-10 was found to be tightly linked to its unpaired status and specific positioning immediately upstream of a RNA: RNA helix formed between the targeting ASO and its intronic target. Employing a heterologous context as well as changed contexts of SMN2 intron 7, we show that the inhibitory effect of unpaired C-10 is dependent upon a long-distance interaction involving downstream intronic sequences. Our report furnishes one of the rare examples in which an ASO-based approach could be applied to unravel the critical role of an intronic position that may not belong to a linear motif and yet play significant role through long-distance interactions.
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