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促甲状腺激素特异性促甲状腺激素β启动子激活的决定因素。Pit-1与另一种因子的协同作用。

Determinants of thyrotrope-specific thyrotropin beta promoter activation. Cooperation of Pit-1 with another factor.

作者信息

Haugen B R, McDermott M T, Gordon D F, Rupp C L, Wood W M, Ridgway E C

机构信息

Department of Medicine, University of Colorado Health Sciences Center, Denver 80262, USA.

出版信息

J Biol Chem. 1996 Jan 5;271(1):385-9. doi: 10.1074/jbc.271.1.385.

Abstract

Thyrotropin (TSH) beta is a subunit of TSH, the expression of which is limited to the thyrotrope cells of the anterior pituitary gland. We have utilized the thyrotrope-derived TtT-97 thyrotropic tumors to investigate tissue-specific expression of the TSH beta promoter. TSH beta promoter activity in thyrotropes is conferred by sequences between -270 and -80 of the 5'-flanking region. We have recently reported that the proximal region from -133 to -100 (P1) is required for promoter expression in thyrotropes. This region interacts with the pituitary-specific transcription factor Pit-1. While Pit-1 appears necessary for TSH beta promoter activity in thyrotropes, this transcription factor is not alone sufficient for promoter activity in pituitary-derived cells. In this report, we have generated a series of promoter mutations in the P1 region to identify additional protein-DNA interactions and determine their functional significance. We have found that Pit-1 interacts with the distal portion of the P1 region, and a second protein interacts with the proximal segment of this region. Each protein is able to independently interact with the TSH beta promoter, but neither alone can maintain promoter activity. Both proteins appear to be necessary for full promoter activity in thyrotropes. Southwestern analysis with the proximal segment of the P1 region (-117 to -88) reveals interaction with a 50-kDa protein. Interestingly, this protein is not found in the pituitary-derived GH3 cells and may represent a thyrotrope-specific transcription factor. Further characterization of this newly identified DNA-binding protein will further our understanding of the tissue-specific expression of the TSH beta gene.

摘要

促甲状腺激素(TSH)β是促甲状腺激素的一个亚基,其表达仅限于垂体前叶的促甲状腺细胞。我们利用源自促甲状腺细胞的TtT-97促甲状腺肿瘤来研究TSHβ启动子的组织特异性表达。促甲状腺细胞中TSHβ启动子活性由5'侧翼区-270至-80之间的序列赋予。我们最近报道,-133至-100(P1)的近端区域是促甲状腺细胞中启动子表达所必需的。该区域与垂体特异性转录因子Pit-1相互作用。虽然Pit-1似乎是促甲状腺细胞中TSHβ启动子活性所必需的,但该转录因子单独不足以维持垂体来源细胞中的启动子活性。在本报告中,我们在P1区域产生了一系列启动子突变,以鉴定额外的蛋白质-DNA相互作用并确定其功能意义。我们发现Pit-1与P1区域的远端部分相互作用,并且第二种蛋白质与该区域的近端部分相互作用。每种蛋白质都能够独立地与TSHβ启动子相互作用,但单独一种都不能维持启动子活性。两种蛋白质似乎都是促甲状腺细胞中完全启动子活性所必需的。用P1区域的近端部分(-117至-88)进行的蛋白质印迹分析显示与一种50 kDa蛋白质相互作用。有趣的是,这种蛋白质在垂体来源的GH3细胞中未发现,可能代表一种促甲状腺细胞特异性转录因子。对这种新鉴定的DNA结合蛋白的进一步表征将加深我们对TSHβ基因组织特异性表达的理解。

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