دورية أكاديمية
A novel cryptic splice site mutation in COL1A2 as a cause of osteogenesis imperfecta.
| العنوان: | A novel cryptic splice site mutation in COL1A2 as a cause of osteogenesis imperfecta. |
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| المؤلفون: | El-Gazzar, A., Mayr, J.A., Voraberger, B., Brügger, K., Blouin, S., Tischlinger, K., Duba, H.C., Prokisch, H., Fratzl-Zelman, N., Högler, W. |
| المصدر: | Bone Rep. 15:101110 (2021) |
| سنة النشر: | 2021 |
| المجموعة: | PuSH - Publikationsserver des Helmholtz Zentrums München |
| مصطلحات موضوعية: | Bone Fragility, Cryptic Splice Site, Mutation, Osteogenesis Imperfecta, Type I Collagen, Whole Exome Sequencing |
| الوصف: | Osteogenesis imperfecta (OI) is an inherited genetic disorder characterized by frequent bone fractures and reduced bone mass. Most cases of OI are caused by dominantly inherited heterozygous mutations in one of the two genes encoding type I collagen, COL1A1 and COL1A2. Here we describe a five-year-old boy with typical clinical, radiological and bone ultrastructural features of OI type I. Establishing the molecular genetic cause of his condition proved difficult since clinical exome and whole exome analysis was repeatedly reported negative. Finally, manual analysis of exome data revealed a silent COL1A2 variant c.3597 T > A (NM_000089.4), which we demonstrate activates a cryptic splice site. The newly generated splice acceptor in exon 50 is much more accessible than the wild-type splice-site between the junction of exon 49 and 50, and results in an in-frame deletion of 24 amino acids of the C-terminal propeptide. In vitro collagen expression studies confirmed cellular accumulation and decreased COL1A2 secretion to 45%. This is the first report of a cryptic splice site within the coding region of COL1A2. which results in abnormal splicing causing OI. The experience from this case demonstrates that routine diagnostic approaches may miss cryptic splicing mutations in causative genes due to the lack of universally applicable algorithms for splice-site prediction. In exome-negative cases, in-depth analysis of common causative genes should be conducted and trio-exome analysis is recommended. |
| نوع الوثيقة: | article in journal/newspaper |
| وصف الملف: | application/pdf |
| اللغة: | English |
| تدمد: | 2352-1872 |
| العلاقة: | info:eu-repo/semantics/altIdentifier/pmid/34381850; info:eu-repo/semantics/altIdentifier/isbn/2352-1872; info:eu-repo/semantics/altIdentifier/pissn/2352-1872; info:eu-repo/semantics/altIden; https://push-zb.helmholtz-muenchen.de/frontdoor.php?source_opus=62701Test; urn:isbn:2352-1872; urn:issn:2352-1872 |
| DOI: | 10.1016/j.bonr.2021.101110 |
| الإتاحة: | https://doi.org/10.1016/j.bonr.2021.101110Test https://push-zb.helmholtz-muenchen.de/frontdoor.php?source_opus=62701Test |
| حقوق: | info:eu-repo/semantics/openAccess |
| رقم الانضمام: | edsbas.ACAC2D0B |
| قاعدة البيانات: | BASE |
Full Text Finder | تدمد: | 23521872 |
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| DOI: | 10.1016/j.bonr.2021.101110 |