A novel -66T/C polymorphism in FcεRI α-chain promoter affecting the transcription activity: Possible relationship to allergic diseases

Masanari Hasegawa, Chiharu Nishiyama, Makoto Nishiyama, Yushiro Akizawa, Kouichi Mitsuishi, Tomonobu Ito, Hiroshi Kawada, Susumu Furukawa, Chisei Ra, Ko Okumura, Hideoki Ogawa

Research output: Contribution to journalArticlepeer-review

71 Citations (Scopus)

Abstract

We found a novel polymorphism, -66T/C, in the promoter region of human FcεRIα, the specific component of the high affinity receptor for IgE (FcεRI), which is essential for the cell surface expression of FcεRI and the binding of IgE Ab. When the effect of the single nucleotide replacement on the promoter function was analyzed, the transcription activity of the T allele promoter was found to be higher than that of the C allele promoter, and was markedly up-regulated by the overexpression of GATA-1 when compared with the C allele promoter. This is probably because the promoter with T at -66 has an additional GATA-1-binding motif in the region, which may assure higher affinity of the transcription factor to the promoter. In accordance with this, EMSA actually indicated that GATA-1 bound to the T allele probe (-80/-59) with the affinity higher than that to the C allele probe. Statistical analysis suggested that a significant portion of nonallergic individuals has heterozygous -66T/C genotype, while most of allergic individuals have homozygous -66T/T genotype in Japanese population. Our findings for the first time demonstrate the presence of FcεRIα polymorphism related to the allergic diseases.

Original languageEnglish
Pages (from-to)1927-1933
Number of pages7
JournalJournal of Immunology
Volume171
Issue number4
DOIs
Publication statusPublished - 15 Aug 2003

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