首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Thyrotropin-releasing hormone regulation of human TSHB expression: role of a pituitary-specific transcription factor (Pit-1/GHF-1) and potential interaction with a thyroid hormone-inhibitory element.
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Thyrotropin-releasing hormone regulation of human TSHB expression: role of a pituitary-specific transcription factor (Pit-1/GHF-1) and potential interaction with a thyroid hormone-inhibitory element.

机译:促甲状腺激素释放激素对人TSHB表达的调节:垂体特异性转录因子(Pit-1 / GHF-1)的作用以及与甲状腺激素抑制因子的潜在相互作用。

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摘要

Regulation of human thyrotropin beta subunit gene (TSHB) expression by thyrotropin-releasing hormone (TRH) was examined in a clonal rat pituitary-cell line (GH3). Transient expression studies were done with various 5'-flanking DNA sequences of TSHB coupled to reporter gene chloramphenicol acetyltransferase. Deletion analysis defined two discrete regions (-128 to -92 base pairs and -28 to +8 base pairs) that each mediated an approximately 2-fold TRH induction. The upstream site contains a DNA sequence with close homology to the DNA-binding site for a pituitary-specific transcriptional factor Pit-1/GHF-1. DNase I footprinting analysis of mouse thyrotropic tumor extract as well as DNA-transfection studies using an expression vector containing an N-terminal deletion of Pit-1/GHF-1 cDNA suggest that Pit-1/GHF-1 or a closely related protein in the thyrotroph mediates TRH responsiveness of this gene. In addition, the downstream site overlaps with the recently characterized thyroid hormone-inhibitory element of TSHB. In fact, deletion of DNA sequences important in thyroid hormone-receptor binding (c-erbAB/c-ERBA2) from +3 to +8 base pairs, significantly reduced (30%) TRH responsiveness. The location of a TRH-stimulatory element near a thyroid hormone-inhibitory element may allow for fine control of TSHB expression in vivo.
机译:在克隆的大鼠垂体细胞系(GH3)中检测了促甲状腺激素释放激素(TRH)对人促甲状腺激素β亚基基因(TSHB)表达的调节。用与报道基因氯霉素乙酰转移酶偶联的TSHB的各种5'侧翼DNA序列进行了瞬时表达研究。缺失分析定义了两个离散的区域(-128至-92个碱基对和-28至+8个碱基对),每个区域介导约2倍的TRH诱导。上游位点包含与垂体特异性转录因子Pit-1 / GHF-1的DNA结合位点具有紧密同源性的DNA序列。小鼠促甲状腺肿瘤提取物的DNase I足迹分析以及使用含有Pit-1 / GHF-1 cDNA N端缺失的表达载体的DNA转染研究表明,Pit-1 / GHF-1或与其密切相关的蛋白甲状腺细胞介导该基因的TRH反应。另外,下游位点与最近表征的TSHB的甲状腺激素抑制元件重叠。实际上,删除对甲状腺激素-受体结合很重要的DNA序列(c-erbAB / c-ERBA2)从+3到+8个碱基对,可显着降低(30%)TRH反应性。甲状腺激素抑制元件附近的TRH刺激元件的位置可能允许体内TSHB表达的精细控制。

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