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甲状腺激素对促甲状腺激素α基因的负调控:与TATA框相邻的受体相互作用

Negative regulation of the thyroid-stimulating hormone alpha gene by thyroid hormone: receptor interaction adjacent to the TATA box.

作者信息

Chatterjee V K, Lee J K, Rentoumis A, Jameson J L

机构信息

Thyroid Unit, Massachusetts General Hospital, Harvard Medical School, Boston 02114.

出版信息

Proc Natl Acad Sci U S A. 1989 Dec;86(23):9114-8. doi: 10.1073/pnas.86.23.9114.

Abstract

Thyroid-stimulating hormone alpha and beta subunit genes are negatively regulated by thyroid hormone at the transcriptional level. Transient gene expression studies were used to demonstrate that the erbA beta form of the thyroid hormone receptor mediates negative regulation of the alpha-subunit promoter in a hormone-dependent manner. In JEG-3 choriocarcinoma cells, which are deficient in thyroid hormone receptors, coexpression of erbA beta with alpha CAT reporter genes markedly suppressed alpha CAT expression after treatment with thyroid hormone, whereas a reporter gene containing a known positive thyroid response element was induced. Thus, a single form of thyroid hormone receptor mediates both positive and negative responses to thyroid hormone in this system. Transient expression analyses of alpha gene 5' flanking sequence deletion mutants localized the negative thyroid response element to the proximal region of the promoter between -100 and +4 base pairs. The location of the negative thyroid response element in the alpha gene is therefore distinct from that of previously identified regulatory elements including the tissue-specific upstream regulatory elements, the cAMP response elements, and the glucocorticoid response elements. Overlapping segments of the alpha promoter were examined for potential thyroid hormone receptor binding sites by using gel shift assays and biotinylated DNA-binding studies. A specific thyroid hormone receptor binding site was identified between -22 and -7 base pairs, which is immediately downstream from the TATA box. This region of the alpha promoter interacts with erbA beta receptor synthesized in vitro as well as with endogenous nuclear thyroid hormone receptors, and it competes for receptor binding to a known positive thyroid response element. These studies suggest a mechanism for negative regulation in which the thyroid hormone receptor interacts with the alpha gene promoter immediately downstream of the TATA box to inhibit transcription.

摘要

促甲状腺激素α和β亚基基因在转录水平受到甲状腺激素的负调控。通过瞬时基因表达研究证明,甲状腺激素受体的erbAβ形式以激素依赖的方式介导α亚基启动子的负调控。在缺乏甲状腺激素受体的JEG-3绒毛膜癌细胞中,erbAβ与αCAT报告基因共表达,在甲状腺激素处理后显著抑制αCAT表达,而含有已知阳性甲状腺反应元件的报告基因则被诱导。因此,在该系统中,单一形式的甲状腺激素受体介导对甲状腺激素的正负反应。对α基因5'侧翼序列缺失突变体的瞬时表达分析将负甲状腺反应元件定位到启动子的近端区域,位于-100至+4碱基对之间。因此,α基因中负甲状腺反应元件的位置与先前鉴定的调控元件不同,包括组织特异性上游调控元件、cAMP反应元件和糖皮质激素反应元件。通过凝胶迁移分析和生物素化DNA结合研究,检查了α启动子的重叠片段是否存在潜在的甲状腺激素受体结合位点。在-22至-7碱基对之间鉴定出一个特定的甲状腺激素受体结合位点,该位点紧邻TATA盒下游。α启动子的这一区域与体外合成的erbAβ受体以及内源性核甲状腺激素受体相互作用,并竞争受体与已知阳性甲状腺反应元件的结合。这些研究提示了一种负调控机制,即甲状腺激素受体与TATA盒下游紧邻的α基因启动子相互作用以抑制转录。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1bc3/298444/adb54827783e/pnas00290-0073-a.jpg

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