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雄激素受体DNA结合结构域决定转录反应的雄激素选择性。

The androgen receptor DNA-binding domain determines androgen selectivity of transcriptional response.

作者信息

Verrijdt G, Tanner T, Moehren U, Callewaert L, Haelens A, Claessens F

机构信息

Laboratory of Molecular Endocrinology, Division of Biochemistry, Campus Gasthuisberg O and N1, Catholic University of Leuven, Herestraat 49, B-3000 Leuven, Belgium.

出版信息

Biochem Soc Trans. 2006 Dec;34(Pt 6):1089-94. doi: 10.1042/BST0341089.

Abstract

The AR (androgen receptor) is a hormone-dependent transcription factor that translates circulating androgen hormone levels into a physiological cellular response by directly regulating the expression of its target genes. It is the key molecule in e.g. the development and maintenance of the male sexual characteristics, spermatocyte production and prostate gland development and growth. It is also a major factor in the onset and maintenance of prostate cancer and a first target for pharmaceutical action against the further proliferation of prostate cancer cells. The AR is a member of the steroid hormone receptors, a group of steroid-inducible transcription factors sharing an identical consensus DNA-binding motif. The problem of how specificity in gene activation is achieved among the different members of this nuclear receptor subfamily is still unclear. In this report, we describe our investigations on how the AR can specifically activate its target genes, while the other steroid hormone receptors do not, despite having the same consensus monomeric DNA-binding motif. In this respect, we describe how the AR interacts with a newly identified class of steroid-response elements to which only the AR and not, for example, the glucocorticoid receptor can bind.

摘要

雄激素受体(AR)是一种激素依赖性转录因子,通过直接调节其靶基因的表达,将循环雄激素激素水平转化为生理细胞反应。它是例如男性性特征的发育和维持、精母细胞产生以及前列腺发育和生长中的关键分子。它也是前列腺癌发生和维持的主要因素,并且是针对前列腺癌细胞进一步增殖的药物作用的首要靶点。AR是类固醇激素受体家族的成员,这是一组共享相同共有DNA结合基序的类固醇诱导型转录因子。在这个核受体亚家族的不同成员中如何实现基因激活的特异性问题仍不清楚。在本报告中,我们描述了我们关于AR如何特异性激活其靶基因的研究,而其他类固醇激素受体尽管具有相同的共有单体DNA结合基序却不能。在这方面,我们描述了AR如何与一类新鉴定的类固醇反应元件相互作用,只有AR能结合这类元件,例如糖皮质激素受体则不能。

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