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人α-胰蛋白酶抑制剂重链H3基因。基因组结构、启动子分析及基因连锁。

Human inter-alpha-trypsin inhibitor heavy chain H3 gene. Genomic organization, promoter analysis, and gene linkage.

作者信息

Diarra-Mehrpour M, Sarafan N, Bourguignon J, Bonnet F, Bost F, Martin J P

机构信息

Laboratoire de Physiopathologie et Génétique Rénale et Pulmonaire, INSERM, Unité 295, Faculté de Médecine, 76183 Rouen Cedex, France.

出版信息

J Biol Chem. 1998 Oct 9;273(41):26809-19. doi: 10.1074/jbc.273.41.26809.

Abstract

To understand more about the human inter-alpha-trypsin inhibitor heavy chain H3 (ITIH3) expression and the relationship between this gene and the family of other ITI heavy chain genes, an analysis of the structure of the ITIH3 gene and its promoter region was performed. This gene is a single copy gene, 14 kilobase pair in length and consists of 22 exons. ITIH3 shares highly conserved exon size and intron-exon borders with other ITI heavy chain genes. We determined that the human ITIH1, ITIH3, and ITIH4 genes are closely linked within a 45-kilobase pair. They are arranged in the order of H1-H3-H4, with the ITIH4 gene transcribed in the opposite direction. A model for the evolution of the ITI heavy chain gene family is presented that involves multiple rounds of gene duplication plus inversion events. The minimum promoter region (-135 to +75) is identified in HepG2 cells. The transient transfection study in various cell lines indicates that the activity of the ITIH3 promoter is not liver-specific. DNase I footprinting, mobility shift assays, and cotransfection experiments reveal a functional CCAAT/enhancer-binding protein site (C/EBP, -1344 to -1305) which interacts with C/EBPalpha and C/EBPbeta factors. The latter factors control the transcription of the ITIH3 gene positively.

摘要

为了更深入了解人类α-胰蛋白酶抑制剂重链H3(ITIH3)的表达情况以及该基因与其他ITI重链基因家族之间的关系,我们对ITIH3基因及其启动子区域的结构进行了分析。该基因是单拷贝基因,长度为14千碱基对,由22个外显子组成。ITIH3与其他ITI重链基因在外显子大小和内含子-外显子边界方面具有高度保守性。我们确定人类ITIH1、ITIH3和ITIH4基因在45千碱基对范围内紧密连锁。它们按H1-H3-H4的顺序排列,其中ITIH4基因转录方向相反。我们提出了一个ITI重链基因家族的进化模型,该模型涉及多轮基因复制和倒位事件。在HepG2细胞中确定了最小启动子区域(-135至+75)。在各种细胞系中的瞬时转染研究表明,ITIH3启动子的活性并非肝脏特异性的。DNA酶I足迹法、迁移率变动分析和共转染实验揭示了一个功能性的CCAAT/增强子结合蛋白位点(C/EBP,-1344至-1305),它与C/EBPα和C/EBPβ因子相互作用。后两种因子对ITIH3基因的转录起正向调控作用。

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