TY - JOUR
T1 - A novel -66T/C polymorphism in FcεRI α-chain promoter affecting the transcription activity
T2 - Possible relationship to allergic diseases
AU - Hasegawa, Masanari
AU - Nishiyama, Chiharu
AU - Nishiyama, Makoto
AU - Akizawa, Yushiro
AU - Mitsuishi, Kouichi
AU - Ito, Tomonobu
AU - Kawada, Hiroshi
AU - Furukawa, Susumu
AU - Ra, Chisei
AU - Okumura, Ko
AU - Ogawa, Hideoki
PY - 2003/8/15
Y1 - 2003/8/15
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=0043136757&partnerID=8YFLogxK
U2 - 10.4049/jimmunol.171.4.1927
DO - 10.4049/jimmunol.171.4.1927
M3 - Article
C2 - 12902495
AN - SCOPUS:0043136757
SN - 0022-1767
VL - 171
SP - 1927
EP - 1933
JO - Journal of Immunology
JF - Journal of Immunology
IS - 4
ER -