A T+6 to C+6 mutation in the donor splice site of COL3A1 IVS7 causes exon skipping and results in Ehlers-Danlos syndrome type IV. Issue 5 (May 1993)

• Record Type: Journal Article
• Authors: Lloyd, J; Narcisi, P; Richards, A; Pope, F M
• Is Part Of: Journal of medical genetics. Volume 30:Issue 5(1993)
• Page Start: 376
• Page End: 380
• Publication Date: 1993-05
• Subjects: Medical genetics -- Periodicals; 616.042
• DOI: 10.1136/jmg.30.5.376
• Languages: English
• ISSNs: 1468-6244

Abstract

Abstract : Ehlers-Danlos syndrome type IV is usually caused by mutations in COL3A1, the gene coding for type III collagen. In a woman with a milder form of this disease, analysis of type III collagen synthesised by her cultured skin fibroblasts showed an apparently shorter form of the protein. Amplification of overlapping cDNAs, encoding the triple helical region of the molecule, showed a deletion near the 5' end of the gene. Sequencing showed that exon 7 was missing from the cDNA sequence. Analysis of genomic DNA showed that this was the result of a T+6 to C+6 mutation in the donor splice site of intron 7. The proband's parents and 35 normal controls were homozygous for T+6 at this position, indicating that the C+6 mutation was causative.