Intracellular degradation of β4 integrin in lethal junctional epidermolysis bullosa with pyloric atresia

A. Micheloni, N. De Luca, G. Tadini, G. Zambruno, Marina D'Alessio

Research output: Contribution to journalArticle

Abstract

Background: Junctional epidermolysis bullosa with pyloric atresia (PA-JEB) is a rare autosomal recessive genodermatosis that manifests with neonatal mucocutaneous blistering and gastric outlet obstruction. The disease, which is caused by mutations in the α6β4 integrin genes (ITGA6, ITGB4), is usually lethal. However, nonlethal cases have also been reported. Mutation database analysis has suggested that premature termination codons predominantly result in lethal forms while missense mutations frequently associate with nonlethal variants. Nevertheless, it is becoming more and more evident that the disease phenotype is also influenced by the position of the mutation in the protein functional domains. Objective: To investigate the molecular basis of a novel PA-JEB lethal case. Methods: Reverse transcriptase-polymerase chain reaction and direct sequencing-based mutation screening were performed. Mutation consequences in the patient's keratinocytes were then analysed by Northern blot and immunoprecipitation. Immunofluorescence analysis of cultured keratinocytes treated with protein intracellular degradation pathway inhibitors was also carried out. Results: The phenotype was caused by the presence, in the homozygous state, of a novel 33 bp in-frame deletion (nucleotides 175-207) in the ITGB4 coding sequence. Despite the normal steady-state level of integrin β4 mRNA, the mutation, designated ΔR59-A69, results in the almost complete absence of α6β4 integrin in the patient's skin and cultured keratinocytes. Exposure of the patient's keratinocytes to the proteasomal inhibitor clasto-lactacystin β-lactone increased the expression of the mutated β4 integrin chains indicating that the proteasome complex is involved in the degradation of the internally deleted β4 polypeptides. Conclusions: We report for the first time a homozygous in-frame deletion in the ITGB4 gene. Our results suggest that the deletion of amino acids R59-A69 interferes with the biosynthetic folding of the protein, leading to a rapid degradation of the mutated β4 chains. These findings provide new insight into the pathogenic effects of mutations affecting different functional domains of the β4 integrin molecule and their prognostic implications in PA-JEB patients.

Original languageEnglish
Pages (from-to)796-802
Number of pages7
JournalBritish Journal of Dermatology
Volume151
Issue number4
DOIs
Publication statusPublished - Oct 2004

Keywords

  • In-frame deletion
  • Integrin β4
  • Junctional epidermolysis bullosa with pyloric atresia
  • Proteasomal degradation

ASJC Scopus subject areas

  • Dermatology

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