Novel mutations, no detectable mRNA and familial genetic analysis of the Wiskott-Aldrich syndrome protein gene in six Japanese patients with Wiskott- Aldrich syndrome

Y. Sasahara, S. Kawai, S. Kumaki, Y. Ohashi, M. Minegishi, S. Tsuchiya

Research output: Contribution to journalArticle

7 Citations (Scopus)

Abstract

The Wiskott-Aldrich syndrome (WAS) is a primary X-linked immunodeficiency disease caused by mutations of the Wiskott-Aldrich syndrome protein (WASP) gene. The present molecular studies of six Japanese was patients identified five different mutations of WASP, including two novel mutations (45delG, 395insGGAGAT), the latter appearing to have occurred de novo. Familial carriers were detected by polymerase chain reaction-single strand conformational polymorphism analysis, restriction enzyme digestion and direct sequencing of PCR products. Neither mRNA nor the protein product were detectable in any of the patients, while various amounts of WASP protein were expressed in carriers, normal controls, haematopoietic cell lines of all lineages and in one patient after receiving allogeneic bone marrow transplantation. Conclusion: Genetic and protein analysis is useful in the definite diagnosis and follow up of Wiskott-Aldrich syndrome patients and in carrier detection, especially of atypical or sporadic patients.

Original languageEnglish
Pages (from-to)23-30
Number of pages8
JournalEuropean Journal of Pediatrics
Volume159
Issue number1-2
DOIs
Publication statusPublished - 2000
Externally publishedYes

Keywords

  • Mutations Carriers Bone marrow transplantation
  • Wiskott-Aldrich syndrome
  • Wiskott-Aldrich syndrome protein

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health

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