Skipping of an exon with a nonsense mutation in the DMD gene is induced by the conversion of a splicing enhancer to a splicing silencer.

Abstract

Modulation of dystrophin pre-mRNA splicing is an attractive strategy to ameliorate the severe phenotype of Duchenne muscular dystrophy (DMD), although this requires a better understanding of the mechanism of splicing regulation. Aberrant splicing caused by gene mutations provides a good model to study splicing regulatory cis-elements and binding proteins. In this study, we identified skipping of in-frame exon 25 induced by a nonsense mutation (NM_004006.2:c.3340A > T;p.Lys1114*) in the DMD gene. Site-directed mutagenesis study in minigenes suggested that c.3340A > T converts an exonic splicing enhancer sequence (ESE) to a silencer element (ESS). Indeed, RNA pull-down and functional study provided evidence that c.3340A > T abolishes the binding of the splicing enhancer protein Tra2β and promotes interactions with the repressor proteins hnRNP A1, hnRNP A2, and hnRNP H. By carefully analyzing the sequence motif encompassing the mutation site, we concluded that the skipping of exon 25 was due to disruption of a Tra2β-dependent ESE and the creation of a new ESS associated with hnRNP A1 and hnRNP A2, which in turn increased the recruitment of hnRNP H to a nearby binding site. Finally, we demonstrated that c.3340A > T impairs the splicing of upstream intron 24 in a splicing minigene assay. In addition, we showed that the correct splicing of exon 25 is finely regulated by multiple splicing regulators that function in opposite directions by binding to closely located ESE and ESS. Our results clarify the detailed molecular mechanism of exon skipping induced by the nonsense mutation c.3340A > T and also provide information on exon 25 splicing.

• Authors: Yanrong Zhu, Huiting Deng, Xiangfa Chen, Hui Li, Cheng Yang, Shuo Li, Xiaoying Pan, Siqi Tian, Shuxin Feng, Xiaoyue Tan, Masafumi Matsuo, Zhujun Zhang
• Journal: Human genetics (Hum Genet) Vol. 138 Issue 7 Pg. 771-785 (Jul 2019) ISSN: 1432-1203 [Electronic] Germany
• PMID: 31168774 (Publication Type: Case Reports, Journal Article)

Chemical References

• DMD protein, human
• Dystrophin

Topics

• Adolescent
• Dystrophin (genetics)
• Enhancer Elements, Genetic
• Exons
• Gene Expression Regulation
• Humans
• Male
• Muscular Dystrophy, Duchenne (genetics, pathology)
• Mutation, Missense
• RNA Splicing
• Silencer Elements, Transcriptional