A novel mutation A1270G of the EDA1 gene causing Tyr343Cys substitution in ectodysplasin-A in a family with anhidrotic ectodermal dysplasia

• Autorzy: Kobielak A. , Kobielak K. , Biedziak B. , Trzeciak W.H.
• Języki publikacji: EN

Abstrakty

EN

The structure of the EDA1 gene was investigated in a patient with anhidrotic ectodermal dysplasia. Sequence analysis revealed a novel A1270G transition in exon 9 of the EDA1 gene in the patient and his uncle, whereas the patient's mother and grandmother were heterozygotes. This mutation resulted in Tyr343Cys substitution in the extracellular domain of the EDA1 gene product — ectodysplasin-A. The addi­tional Cys343 was located between Cys332 and Cys346 and formed with Cys352 a cluster of four closely situated residues that could potentially form disulfide bonds. This mutation might affect the tertiary structure of the receptor-binding domain of ectodysplasin-A and precipitate the clinical symptoms of anhidrotic ectodermal dysplasia.

Słowa kluczowe

EN

dysplasia; anhidrotic ectodermal dysplasia; clinical symptom; EDA1 gene; mutation; ectodysplasin-A

• Wydawca: -
• Czasopismo: Acta Biochimica Polonica
• Rocznik: 2003
• Tom: 50
• Numer: 1
• Opis fizyczny: p.255-258,fig.

Twórcy

autor

Kobielak A.

• University of Medical Sciences, Swiecickiego 6, 60-781 Poznan, Poland

autor

Kobielak K.

autor

Biedziak B.

autor

Trzeciak W.H.

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