Takahashi Kyoko, Nishiyama Chiharu, Hasegawa Masanari, Akizawa Yushiro, Ra Chisei
Division of Molecular Cell Immunology and Allergology, Nihon University Graduate School of Medical Sciences, 30-1 Oyaguchi, Kami-machi, Itabashi-ku, Tokyo 173-8610, Japan.
J Immunol. 2003 Sep 1;171(5):2478-84. doi: 10.4049/jimmunol.171.5.2478.
The high affinity IgE receptor, FcepsilonRI, is a key regulatory molecule in the allergic reaction. By screening for cis-acting elements over the entire region of the human FcepsilonRI beta-chain gene, a sequence located in the fourth intron was revealed to serve as a repressor element. This element was recognized by a transcription factor, myeloid zinc finger protein 1 (MZF-1). Introduction of MZF-1 antisense inhibited the suppressive effect of the element on the beta-chain promoter and increased the mRNA for the beta-chain in KU812 cells, indicating that MZF-1 repressed human FcepsilonRI beta-chain gene expression via the element in the fourth intron. Furthermore, it was suggested that a cofactor binding with MZF-1, whose expression level was different among the cell types, was required for transcriptional repression by MZF-1.
高亲和力IgE受体FcepsilonRI是过敏反应中的关键调节分子。通过筛选人类FcepsilonRIβ链基因整个区域的顺式作用元件,发现位于第四内含子的一个序列可作为抑制元件。该元件可被转录因子髓系锌指蛋白1(MZF-1)识别。导入MZF-1反义核酸可抑制该元件对β链启动子的抑制作用,并增加KU812细胞中β链的mRNA水平,表明MZF-1通过第四内含子中的元件抑制人类FcepsilonRIβ链基因的表达。此外,还表明MZF-1进行转录抑制需要一个与MZF-1结合的辅因子,其表达水平在不同细胞类型中有所不同。