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Updated: Mar 10, 2026

Evaluation of Exon Inclusion Induced by Splice Switching Antisense Oligonucleotides in SMA Patient Fibroblasts
Published on: May 11, 2018
Alternative splicing of a cryptic exon embedded in intron 6 of SMN1 and SMN2
Satomi Yoshimoto1, Nur Imma Fatimah Harahap1, Yuko Hamamura1
1Department of Community Medicine and Social Healthcare Science, Kobe University Graduate School of Medicine , Kobe, Japan.
Abstract:
Both survival of motor neuron (SMN) genes are associated with spinal muscular atrophy; mutations in SMN1 cause the disease, and SMN2 modulates its severity. It is established that different alternative splicing of exon 7 occurs for SMN1 and SMN2, and a cryptic exon was recently found in intron 6 of both genes. Here, we characterize this cryptic exon and clarify its alternative splicing pattern in control and spinal muscular atrophy cells.
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