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雌二醇调节人糖蛋白激素α亚基基因的甲状腺激素调控。

Estradiol modulates thyroid hormone regulation of the human glycoprotein hormone alpha subunit gene.

作者信息

Yarwood N J, Gurr J A, Sheppard M C, Franklyn J A

机构信息

Department of Medicine, University of Birmingham, Queen Elizabeth Hospital, Edgbaston, United Kingdom.

出版信息

J Biol Chem. 1993 Oct 15;268(29):21984-9.

PMID:7691820
Abstract

We have examined mechanisms of regulation of the human glycoprotein hormone alpha subunit gene by thyroid hormone (T3) and estradiol. Pituitary-derived GH3 cells were transiently transfected with chimeric constructs comprising between 1,500 and 98 base pairs of human alpha subunit gene 5'-flanking sequence fused to the bacterial gene encoding chloramphenicol acetyltransferase (h alpha CAT) and treated with T3 and estradiol, alone and in combination. In pituitary cells, 98 base pairs of alpha gene 5'-flanking sequence were sufficient to mediate both inhibition of alpha gene promoter activity by T3 and stimulation by estradiol; inhibition of the alpha promoter by T3 was antagonized by estradiol. Mutation of nucleotides essential for T3 receptor binding to the alpha gene thyroid hormone response element abolished the response of h alpha CAT expression to estradiol as well as T3. In contrast to pituitary GH3 cells, estradiol treatment alone had no effect on expression of either h alpha CAT or the endogenous alpha gene in JEG-3 choriocarcinoma cells cotransfected with a human thyroid hormone receptor expression vector, but estradiol antagonized suppression of both endogenous and transfected alpha promoter activity by T3. Gel mobility shift assays demonstrated specific binding of in vitro synthesized human estrogen receptor (ER) to the alpha gene thyroid hormone response element. These findings suggest that estradiol modulates expression of the human alpha subunit gene in pituitary and choriocarcinoma cells by direct binding of ER to the alpha gene promoter, and that interaction of ER with the alpha gene negative TRE accounts for the antagonistic effects of estradiol and T3.

摘要

我们研究了甲状腺激素(T3)和雌二醇对人糖蛋白激素α亚基基因的调控机制。用包含1500至98个碱基对的人α亚基基因5'侧翼序列与编码氯霉素乙酰转移酶的细菌基因(hαCAT)融合的嵌合构建体瞬时转染垂体来源的GH3细胞,并单独或联合用T3和雌二醇处理。在垂体细胞中,98个碱基对的α基因5'侧翼序列足以介导T3对α基因启动子活性的抑制以及雌二醇的刺激作用;T3对α启动子的抑制作用被雌二醇拮抗。T3受体与α基因甲状腺激素反应元件结合所必需的核苷酸突变消除了hαCAT表达对雌二醇以及T3的反应。与垂体GH3细胞不同,单独用雌二醇处理对与人甲状腺激素受体表达载体共转染的JEG-3绒毛膜癌细胞中hαCAT或内源性α基因的表达均无影响,但雌二醇拮抗T3对内源性和转染的α启动子活性的抑制作用。凝胶迁移率变动分析表明体外合成的人雌激素受体(ER)与α基因甲状腺激素反应元件特异性结合。这些发现表明,雌二醇通过ER直接与α基因启动子结合来调节垂体和绒毛膜癌细胞中人α亚基基因的表达,并且ER与α基因负性甲状腺激素反应元件的相互作用解释了雌二醇和T3的拮抗作用。

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