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雄激素与糖皮质激素受体异二聚体的形成。转录活性相互抑制的一种可能机制。

Androgen and glucocorticoid receptor heterodimer formation. A possible mechanism for mutual inhibition of transcriptional activity.

作者信息

Chen S y, Wang J, Yu G q, Liu W, Pearce D

机构信息

Division of Nephrology, Department of Medicine, San Francisco General Hospital, and Biomedical Sciences Program, University of California, San Francisco, California 94143, USA.

出版信息

J Biol Chem. 1997 May 30;272(22):14087-92. doi: 10.1074/jbc.272.22.14087.

Abstract

The androgen and glucocorticoid hormones elicit divergent and often opposing effects in cells, tissues, and animals. A wide range of physiological and molecular biological evidence suggests that the receptors that mediate these effects, the androgen and glucocorticoid receptors (AR and GR, respectively), influence each other's transcriptional activity. We now show that coexpressed AR and GR indeed do interact at the transcriptional level and that this interaction is correlated with their ability to form heterodimers at a common DNA site, in vitro and in vivo. Furthermore, mutants that cannot heterodimerize do not inhibit each other's activity. These observations provide the first evidence that the opposing physiological effects of the androgen and glucocorticoid hormones are due to the direct physical interaction between their receptors at the transcriptional level.

摘要

雄激素和糖皮质激素在细胞、组织及动物体内会引发不同且往往相反的效应。大量生理和分子生物学证据表明,介导这些效应的受体,即雄激素受体和糖皮质激素受体(分别为AR和GR),会相互影响对方的转录活性。我们现在证明,共表达的AR和GR确实在转录水平上相互作用,且这种相互作用与其在体外和体内于共同DNA位点形成异二聚体的能力相关。此外,无法形成异二聚体的突变体不会抑制彼此的活性。这些观察结果首次证明,雄激素和糖皮质激素的相反生理效应是由于其受体在转录水平上的直接物理相互作用所致。

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