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通过一个内含子元件对人高亲和力IgE受体β链基因表达的调控

Regulation of the human high affinity IgE receptor beta-chain gene expression via an intronic element.

作者信息

Takahashi Kyoko, Nishiyama Chiharu, Hasegawa Masanari, Akizawa Yushiro, Ra Chisei

机构信息

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.

出版信息

J Immunol. 2003 Sep 1;171(5):2478-84. doi: 10.4049/jimmunol.171.5.2478.

Abstract

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.

摘要

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。

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