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维甲酸受体之间的拮抗作用。

Antagonism between retinoic acid receptors.

作者信息

Husmann M, Lehmann J, Hoffmann B, Hermann T, Tzukerman M, Pfahl M

机构信息

Cancer Center, La Jolla Cancer Research Foundation, California 92037.

出版信息

Mol Cell Biol. 1991 Aug;11(8):4097-103. doi: 10.1128/mcb.11.8.4097-4103.1991.

Abstract

In the developing mouse, retinoic acid receptors (RARs) beta and gamma 1 are expressed in characteristic spatiotemporal patterns which are correlated with different developmental fates of the respective tissues. Understanding the cues that regulate the expression of the various RARs may therefore provide insights into the process of tissue diversification. Transcription of RAR beta is rapidly upregulated through a retinoic acid-responsive element (here referred to as the beta RARE) in its promoter. Like RAR alpha and RAR beta, RAR gamma 1 has been implicated in the activation of the beta RARE. Therefore, it is puzzling that RAR beta and RAR gamma 1 appear to be expressed in reciprocal patterns. In the present report, we show that RAR gamma 1, one of the two predominant RAR gamma isoforms, can inhibit the activity of RAR gamma 2, RAR beta, and endogenous RAR on the beta RARE. In contrast, the three RAR gamma isoforms tested and RAR beta activated a palindromic thyroid hormone response element with similar levels of efficiency. The differential activity of RAR gamma 1 compared with that of RAR beta appears to reside in both the N-terminal and the C-terminal halves of RAR gamma 1. RAR gamma 1-mediated inhibition of other RARs may involve competition for the response element as well as direct interaction with other receptors and might be part of a regulatory system contributing to the characteristic tissue distribution of the various RARs.

摘要

在发育中的小鼠体内,维甲酸受体(RARs)β和γ1以特定的时空模式表达,这与各组织不同的发育命运相关。因此,了解调控各种RARs表达的线索可能有助于深入了解组织分化过程。RARβ的转录通过其启动子中的维甲酸反应元件(以下称为βRARE)迅速上调。与RARα和RARβ一样,RARγ1也参与βRARE的激活。然而,令人费解的是,RARβ和RARγ1似乎以相反的模式表达。在本报告中,我们表明,两种主要的RARγ亚型之一的RARγ1能够抑制RARγ2、RARβ以及内源性RAR对βRARE的活性。相比之下,所测试的三种RARγ亚型和RARβ对回文甲状腺激素反应元件的激活效率相似。与RARβ相比,RARγ1的差异活性似乎存在于RARγ1的N端和C端。RARγ1介导的对其他RARs的抑制可能涉及对反应元件的竞争以及与其他受体的直接相互作用,并且可能是有助于各种RARs特征性组织分布的调节系统的一部分。

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