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非洲爪蟾TRβ基因的转录抑制是由位于起始位点附近的甲状腺激素反应元件介导的。

Transcriptional repression of Xenopus TR beta gene is mediated by a thyroid hormone response element located near the start site.

作者信息

Ranjan M, Wong J, Shi Y B

机构信息

Laboratory of Molecular Embryology, NICHHD, National Institutes of Health, Bethesda, Maryland 20892.

出版信息

J Biol Chem. 1994 Oct 7;269(40):24699-705.

PMID:7929143
Abstract

We report here the detailed analysis of the promoter of a thyroid hormone receptor (TR) gene that is regulated by the hormone itself. The receptor gene, TR beta A, is one of the two TR beta genes in Xenopus laevis. It has two transcription start sites. The mRNAs derived from one of them are up-regulated by thyroid hormone, whereas those derived from the other are independent of the hormone. We have characterized the hormone-inducible promoter using a transient transfection assay in a Xenopus tissue culture cell line (A6). Deletion and mutational analysis identifies the first amphibian thyroid hormone response element (TRE). This TRE consists of near perfect direct repeats of AGGTCA with a 4-base pair spacing similar to mammalian TREs. The TRE forms specific complexes with extracts of A6 cells that have similar sequence specificities as those found for the complexes between mammalian TRs and TREs. However, unlike TREs found in other thyroid hormone-inducible promoters, this TRE is located at the putative transcription start site and mediates transcriptional repression by unliganded TRs. The addition of thyroid hormone at physiological concentrations overcomes the repression and induces further transcriptional activation at higher concentrations. These results suggest a potential mechanism for the regulation of amphibian metamorphosis, a process that is entirely controlled by thyroid hormone.

摘要

我们在此报告对一种受甲状腺激素自身调控的甲状腺激素受体(TR)基因启动子的详细分析。该受体基因TRβA是非洲爪蟾(Xenopus laevis)中两个TRβ基因之一。它有两个转录起始位点。其中一个转录起始位点产生的mRNA受甲状腺激素上调,而另一个产生的mRNA则不受激素影响。我们利用非洲爪蟾组织培养细胞系(A6)中的瞬时转染试验对激素诱导型启动子进行了表征。缺失和突变分析确定了首个两栖类甲状腺激素反应元件(TRE)。这个TRE由近乎完美的AGGTCA直接重复序列组成,间隔为4个碱基对,类似于哺乳动物的TRE。该TRE与A6细胞提取物形成特异性复合物,其序列特异性与哺乳动物TR和TRE之间形成的复合物相似。然而,与其他甲状腺激素诱导型启动子中的TRE不同,这个TRE位于假定的转录起始位点,并介导未结合配体的TR的转录抑制。在生理浓度下添加甲状腺激素可克服这种抑制,并在更高浓度下诱导进一步的转录激活。这些结果提示了一种调控两栖类变态发育的潜在机制,两栖类变态发育过程完全受甲状腺激素控制。

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