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人类表面活性蛋白B基因的上游增强子活性由甲状腺转录因子1介导。

Upstream enhancer activity in the human surfactant protein B gene is mediated by thyroid transcription factor 1.

作者信息

Yan C, Sever Z, Whitsett J A

机构信息

Children's Hospital Medical Center, Division of Pulmonary Biology, Cincinnati, Ohio 45229-3039, USA.

出版信息

J Biol Chem. 1995 Oct 20;270(42):24852-7. doi: 10.1074/jbc.270.42.24852.

Abstract

Surfactant protein B (SP-B) is selectively expressed in bronchiolar and alveolar epithelial cells of the lung. We identified an upstream enhancer located in the 5'-flanking region of the human SP-B gene (-439 to -331 base pair, hSP-B(-439/-331)) by deletion analysis of SP-B-luciferase constructs assessed in transfection assays in vitro. The element cis-activated the expression of an SV40 promoter-luciferase reporter gene in a human pulmonary adenocarcinoma cell line (H441-4). Three distinct binding sites for the nuclear transcription protein, thyroid transcription factor 1 (TTF-1), were identified, and the purified TTF-1 homeodomain was bound to bhe region of hSP-B(-439/-331). Co-transfection of H441-4 cells with the expression vector pCMV-TTF-1 trans-activated the native human SP-B promoter and the SV40 promoter fused with the SP-B enhancer. Mutations of the TTF-1 binding sites in the upstream enhancer blocked TTF-1 binding and transactivation activity. In summary, TTF-1 interacts with distinct proximal (-80 to -110) and distal (-439 to -331) cis-acting elements than regulate lung epithelial cell-specific transcription of the human SP-B gene.

摘要

表面活性蛋白B(SP-B)在肺的细支气管和肺泡上皮细胞中选择性表达。我们通过对体外转染实验中评估的SP-B-荧光素酶构建体进行缺失分析,在人SP-B基因的5'-侧翼区域(-439至-331碱基对,hSP-B(-439 / -331))中鉴定出一个上游增强子。该元件在人肺腺癌细胞系(H441-4)中顺式激活了SV40启动子-荧光素酶报告基因的表达。鉴定出了核转录蛋白甲状腺转录因子1(TTF-1)的三个不同结合位点,并且纯化的TTF-1同源结构域与hSP-B(-439 / -331)的该区域结合。用表达载体pCMV-TTF-1共转染H441-4细胞可反式激活天然人SP-B启动子和与SP-B增强子融合的SV40启动子。上游增强子中TTF-1结合位点的突变阻断了TTF-1结合和反式激活活性。总之,TTF-1与不同的近端(-80至-110)和远端(-439至-331)顺式作用元件相互作用,从而调节人SP-B基因的肺上皮细胞特异性转录。

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