Different phenotypes in recessive dystrophic epidermolysis bullosa patients sharing the same mutation in compound heterozygosity with two novel mutations in the type vii collagen gene

R. Gardella, N. Zoppi, G. Zambruno, S. Barlati, M. Colombi

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Abstract

Background: Dystrophic epidermolysis bullosa (DEB) is a bullous skin disease caused by mutations in the type VII collagen gene (COL7A1). Objectives: To elucidate the mutations shown by two patients with DEB and understand the clinical phenotypes that they displayed. Methods: We have characterized two patients, one affected by the severe recessive Hallopeau-Siemens variant of DEB (HS-RDEB) and the other by a milder recessive DEB form. Results: In both patients we identified the R2063W missense mutation. The second mutation, in the HS-RDEB patient, was a novel 344insG, leading to a premature termination codon of translation (PTC) in exon 3, while, in the other patient, it was a novel 4965C → T transition, which creates a new donor splice site in exon 53. The effect of this anomalous splice site leads to the maturation of a 17-nucleotides-deleted mRNA containing a PTC. In addition to this aberrant transcript, a certain amount of full-length mRNA is also generated from the mutated pre-mRNA through splicing at the canonical site. Conclusions: In these patients therefore the severity of the phenotype depends on the second mutation. In the patient with the 344insG mutation, leading to a PTC, type VII collagen (COLVII) molecules are exclusively composed of chains containing the R2063W substitution; as a consequence, all anchoring fibrils (AF) are abnormal and the phenotype is severe. In the other patient, the 4965C → T splicing mutation allows the synthesis of a certain quantity of normal chains and the consequent assembly of partially functional COLVII molecules and AF, thus explaining the mild phenotype.

Original languageEnglish
Pages (from-to)450-457
Number of pages8
JournalBritish Journal of Dermatology
Volume147
Issue number3
DOIs
Publication statusPublished - 2002

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Keywords

  • COL7A1
  • Epidermolysis bullosa dystrophica
  • Genotype-phenotype correlation
  • Missense mutation
  • Splicing mutation

ASJC Scopus subject areas

  • Dermatology

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