Tanner Tamzin, Claessens Frank, Haelens Annemie
Biochemistry Division, Laboratory of Molecular Endocrinology, Catholic University of Leuven, Campus Gasthuisberg O&N, Herestraat 49, Leuven, 3000, Belgium.
Ann N Y Acad Sci. 2004 Dec;1030:587-92. doi: 10.1196/annals.1329.068.
To investigate the function of the hinge region in transcriptional activation by the androgen receptor, we compared the actions of the wild-type receptor with a mutant receptor, deleted of amino acids 628-646 of the hinge. The role of the proteasome on the expression and activity of these two proteins was investigated. The deletion mutant demonstrated a threefold increase in transcriptional activity when compared to the wild-type receptor protein. Furthermore, we found that hormone-dependent stabilization of the receptor protein was more enhanced for the deletion mutant. In addition, experiments using the proteasome inhibitor, MG132, demonstrated that the deletion mutant is more sensitive to proteasome-mediated degradation than the wild-type receptor. However, inhibition of the proteasome had a negative effect on the transcriptional activity of the deletion mutant. Taken together, our results suggest that the hinge region not only plays an important role in controlling the transactivation potential of the androgen receptor but also in determining the influence of the proteasome on androgen receptor-mediated transcriptional activation.
为了研究铰链区在雄激素受体转录激活中的作用,我们比较了野生型受体与缺失铰链区628 - 646位氨基酸的突变型受体的作用。研究了蛋白酶体对这两种蛋白表达和活性的作用。与野生型受体蛋白相比,缺失突变体的转录活性增加了三倍。此外,我们发现缺失突变体的受体蛋白的激素依赖性稳定性增强更为明显。另外,使用蛋白酶体抑制剂MG132的实验表明,缺失突变体比野生型受体对蛋白酶体介导的降解更敏感。然而,蛋白酶体的抑制对缺失突变体的转录活性有负面影响。综上所述,我们的结果表明,铰链区不仅在控制雄激素受体的反式激活潜能中起重要作用,而且在确定蛋白酶体对雄激素受体介导的转录激活的影响中也起重要作用。