Maeda Keiko, Nishiyama Chiharu, Tokura Tomoko, Akizawa Yushiro, Nishiyama Makoto, Ogawa Hideoki, Okumura Ko, Ra Chisei
Atopy (Allergy) Research Center, Juntendo University School of Medicine, University of Tokyo, Japan.
J Immunol. 2003 Jan 1;170(1):334-40. doi: 10.4049/jimmunol.170.1.334.
The FcR beta-chain, a subunit of two related multisubunit receptor complexes, the FcepsilonRI and FcgammaRIII, amplifies the mast cell response and is necessary for the cell surface expression of FcepsilonRI in mouse. The transient reporter assay indicated that -69/+4 region is required for cell type-specific transcriptional regulation of mouse beta-chain gene. EMSA using Abs against transcription factors or competitive oligonucleotides demonstrated that -58/-40 region (containing overlapping three GATA-1 sites, -53/-48, -46/-51, and -42/-47) and -31/-26 region (containing one GATA-1 site) are recognized by GATA-1. The promoter activity of beta-chain was decreased by nucleotide replacements of the GATA-1 sites in mouse mast cell line PT18. Furthermore, exogenously produced GATA-1 up-regulated the promoter activity in CV-1 cells, which are negative in the beta-chain production and the up-regulation was apparently suppressed by GATA-1 site mutations. These results indicate that cell type-specific transcription of mouse beta-chain gene is regulated by GATA-1.
FcRβ链是两种相关的多亚基受体复合物(FcεRI和FcγRIII)的一个亚基,它能放大肥大细胞反应,并且对小鼠FcεRI的细胞表面表达是必需的。瞬时报告基因检测表明,-69/+4区域对于小鼠β链基因的细胞类型特异性转录调控是必需的。使用针对转录因子的抗体或竞争性寡核苷酸进行的电泳迁移率变动分析(EMSA)表明,-58/-40区域(包含三个重叠的GATA-1位点,-53/-48、-46/-51和-42/-47)和-31/-26区域(包含一个GATA-1位点)可被GATA-1识别。在小鼠肥大细胞系PT18中,β链的启动子活性因GATA-1位点的核苷酸替换而降低。此外,外源性产生的GATA-1上调了CV-1细胞中的启动子活性,CV-1细胞不产生β链,且这种上调明显受到GATA-1位点突变的抑制。这些结果表明,小鼠β链基因的细胞类型特异性转录受GATA-1调控。