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α-Pal/NRF-1调控人整合素相关蛋白/CD47基因的启动子。

Alpha-Pal/NRF-1 regulates the promoter of the human integrin-associated protein/CD47 gene.

作者信息

Chang Wen-Teng, Huang A-Min

机构信息

Institute of Basic Medical Sciences, National Cheng Kung University, Medical College, Tainan 701, Taiwan.

出版信息

J Biol Chem. 2004 Apr 9;279(15):14542-50. doi: 10.1074/jbc.M309825200. Epub 2004 Jan 27.

DOI:10.1074/jbc.M309825200
PMID:14747477
Abstract

Integrin-associated protein (IAP or CD47) is expressed in a variety of tissues, including the nervous system and immune system. To understand how cells control the expression of the IAP gene, we cloned the 5'-proximal region of the human IAP gene and investigated IAP promoter activity by transient transfection. RT-PCR confirmed the expression of IAP transcripts in human neuroblastoma IMR-32 and hepatoma HepG2 cells. Deletion analysis identified a core promoter of the human IAP gene located between nucleotide positions -232 and -12 relative to the translation initiation codon in these two cell lines. Site-directed mutagenesis and gel electrophoretic mobility shift assay identified a alpha-Pal/NRF-1 binding element within the IAP core promoter. Supershift assays using the alpha-Pal/NRF-1 antiserum confirmed the binding of this transcription factor on the alpha-Pal/NRF-1 site. Overexpression of the DNA binding domain of alpha-Pal/NRF-1 in cells enhanced DNA-alpha-Pal/NRF-1 binding in vitro. Furthermore, overexpression of full-length alpha-Pal/NRF-1 significantly enhanced IAP promoter activity while overexpression of dominant-negative mutant reduced promoter activity both in the cultured human cell lines and primary mouse cortical cells. These results revealed that alpha-Pal/NRF-1 is an essential transcription factor in the regulation of human IAP gene expression.

摘要

整合素相关蛋白(IAP或CD47)在包括神经系统和免疫系统在内的多种组织中表达。为了解细胞如何控制IAP基因的表达,我们克隆了人类IAP基因的5'近端区域,并通过瞬时转染研究了IAP启动子活性。逆转录聚合酶链反应(RT-PCR)证实了IAP转录本在人神经母细胞瘤IMR-32和肝癌HepG2细胞中的表达。缺失分析确定了在这两种细胞系中,相对于翻译起始密码子,人类IAP基因的核心启动子位于核苷酸位置-232至-12之间。定点诱变和凝胶电泳迁移率变动分析确定了IAP核心启动子内的一个α-Pal/NRF-1结合元件。使用α-Pal/NRF-1抗血清的超迁移分析证实了该转录因子在α-Pal/NRF-1位点的结合。在细胞中过表达α-Pal/NRF-1的DNA结合结构域增强了体外DNA-α-Pal/NRF-1的结合。此外,在培养的人类细胞系和原代小鼠皮质细胞中,全长α-Pal/NRF-1的过表达显著增强了IAP启动子活性,而显性负性突变体的过表达则降低了启动子活性。这些结果表明,α-Pal/NRF-1是调节人类IAP基因表达的必需转录因子。

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