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Severe Darier's Disease by Mitochondrial DNA Insertion Causing Nonsense Mutations: In Silico Prediction of a
Haruna Shintani1, Yasuaki Ikuno1,2, Hiraku Kokubu1
1Department of Dermatology, Shiga University of Medical Science, Otsu, Shiga, Japan.
Abstract:
Darier's disease (DD) is an autosomal dominant genetic disorder caused by mutations in ATP2A2. Several cases with nonsense ATP2A2 mutations presented mild-to-moderate phenotypes despite the presumed larger deletion sizes of the ATP2A2 protein. Here, we report a case of severe DD caused by a nonsense mutation with a mitochondrial DNA (mtDNA) insertion despite the smaller presumed deletion size of the ATP2A2 protein. In silico analyses of genomic lesions forming non-B DNA structures and sequence homology indicated the contingency of this DNA insertion. Analysis of the three-dimensional structure of the protein predicted no structural disturbance by this insertion. However, the QGRS Mapper algorithm predicted ectopic G-quadruplex formation in the inserted genome, which may possibly reduce ATP2A2 transcription. Consistent with this hypothetical mechanism and possible nonsense-mediated mRNA decay, we identified downregulation of the mtDNA-inserted ATP2A2, which may partially contribute to the severe phenotype in this case. The mtDNA insertions into the human genome are reported to rarely occur, especially in cancers, and only a handful of mtDNA insertions causing genetic diseases are described. This study is the first report to identify mtDNA insertion as a cause of genetic disease in dermatology and demonstrates its pathophysiological mechanism through in silico analyses.
Insights
Darier's disease can be severe due to mitochondrial DNA insertions affecting ATP2A2 gene transcription. This study identifies a novel genetic mechanism contributing to severe Darier's disease phenotypes.
Area of Science:
- Genetics
- Molecular Biology
- Dermatology
Background:
- Darier's disease (DD) is an autosomal dominant disorder caused by ATP2A2 mutations.
- Nonsense mutations in ATP2A2 typically correlate with milder phenotypes, irrespective of deletion size.
Observation:
- A severe DD case presented with a nonsense ATP2A2 mutation and a mitochondrial DNA (mtDNA) insertion.
- In silico analysis suggested the insertion could lead to ectopic G-quadruplex formation, potentially reducing ATP2A2 transcription.
Findings:
- The study identified downregulation of the mtDNA-inserted ATP2A2, correlating with the severe phenotype.
- This mechanism, involving mtDNA insertion and subsequent gene downregulation, is novel in dermatological genetic diseases.
Implications:
- This finding expands the known genetic causes of Darier's disease.
- It highlights mtDNA insertions as a rare but significant etiological factor in genetic disorders.
- The study provides a potential mechanism for severe DD phenotypes linked to mtDNA insertions.
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