雄激素受体
交易激励
基因敲除
化学
免疫沉淀
泛素
泛素连接酶
二氢睾酮
HEK 293细胞
转录因子
受体
细胞生物学
分子生物学
癌症研究
雄激素
生物
生物化学
基因
遗传学
前列腺癌
癌症
激素
作者
Shuliang Chen,Ke Chen,Qinghua Zhang,Hanhua Cheng,Rongjia Zhou
摘要
Loss and/or inactivation of the VHL (von Hippel-Lindau) tumour suppressor causes various tumours. Using a yeast two-hybrid system, we have identified the AR (androgen receptor) co-activator UXT (ubiquitously expressed transcript), as a VHL-interacting protein. GST pull-down and co-immunoprecipitation assays show that UXT interacts with VHL. In addition, UXT recruits VHL to the nucleus. VHL associates with the DBD (DNA-binding domain) and hinge domains of the AR and induces AR ubiquitination. Moreover, VHL interaction with the AR activates AR transactivation upon DHT (dihydrotestosterone) treatment. VHL knockdown inhibits AR ubiquitination and decreases transcriptional activation of the AR. Our data suggest that the VHL-UXT interaction and VHL-induced ubiquitination of AR regulate transcriptional activation of the AR.
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