Faculty of Pharmaceutical Sciences, Toho University, Chiba, Japan.
Biochem Biophys Res Commun. 2012 Sep 14;426(1):38-42. doi: 10.1016/j.bbrc.2012.08.027. Epub 2012 Aug 13.
The constitutive androstane receptor (CAR) plays a key role in the expression of xenobiotic/steroid and drug metabolizing enzymes and their transporters. In this study, we demonstrated that DP97, a member of the DEAD box DNA/RNA helicase protein family, is a novel CAR-interacting protein. Using HepG2 cells expressing human CAR in the presence of tetracycline, we showed that knockdown of DP97 with small interfering RNAs suppressed tetracycline-inducible mRNA expression of CYP2B6 and UGT1A1 but not CYP3A4. Thus, DP97 was found to be a gene (or promoter)-selective co-activator for hCAR. DP97-mediated CAR transactivation was synergistically enhanced by the co-expression of SRC-1 or PGC1α, therefore it might act as mediator between hCAR and appropriate co-activators.
组成型雄烷受体(CAR)在异源生物/甾体和药物代谢酶及其转运蛋白的表达中发挥关键作用。在这项研究中,我们证明了 DEAD 盒 DNA/RNA 解旋酶蛋白家族的成员 DP97 是一种新型的 CAR 相互作用蛋白。使用在四环素存在下表达人 CAR 的 HepG2 细胞,我们表明,用小干扰 RNA 敲低 DP97 抑制了四环素诱导的 CYP2B6 和 UGT1A1 但不 CYP3A4 的 mRNA 表达。因此,DP97 被发现是 hCAR 的基因(或启动子)选择性共激活子。DP97 介导的 CAR 反式激活通过 SRC-1 或 PGC1α 的共表达协同增强,因此它可能充当 hCAR 和适当共激活子之间的介质。