Three novel integrin β3 subunit missense mutations (H280P, C560F, and G579S) in thrombasthenia, including one (H280P) prevalent in Japanese patients

Hironobu Ambo, Tetsuji Kamata, Makoto Handa, Masashi Taki, Minoru Kuwajima, Yohko Kawai, Atsushi Oda, Mitsuru Murata, Yoshikazu Takada, Kiyoaki Watanabe, Yasuo Ikeda

Research output: Contribution to journalArticle

36 Citations (Scopus)

Abstract

We analyzed three unrelated Japanese patients with type II Glanzmann thrombasthenia (GT) for associated mutations. Polymerase chain reaction and subsequent direct sequencing of platelet RNA and genomic DNA revealed three single nucleotide substitutions of the integrin β3 subunit gene (His (CAT)-280 to Pro (CCT), Cys (TGT)-560 to Phe (TTT), and Gly(GGC)-579 to Ser(AGC)). Interestingly, the three unrelated patients all had the H280P mutation; one was homozygous and the other two heterozygous for this mutation. Ectopic expression of wild type and mutant complexes in Chinese hamster ovary cells revealed decreased surface expression of the mutated αIIbβ3 complexes, thus demonstrating that these mutations may result in the mild GT phenotypes. The identification of three unrelated patients having the same mutation (H280P) suggests that this mutation might be prevalent in the Japanese thrombasthenic population.

Original languageEnglish
Pages (from-to)763-768
Number of pages6
JournalBiochemical and Biophysical Research Communications
Volume251
Issue number3
DOIs
Publication statusPublished - 1998 Oct 29

ASJC Scopus subject areas

  • Biophysics
  • Biochemistry
  • Molecular Biology
  • Cell Biology

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