组成型雄激素受体新变体(CAR,NR1I3)的功能表征

V. Prantner, Y. Cinnamon, Jenni Küblbeck, Ferdinand Molnár, P. Honkakoski
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引用次数: 0

摘要

核受体组成型雄烷受体(CAR;NR1I3)控制许多参与药物代谢和运输、能量代谢和毒性的酶和转运体的诱导表达。CAR的单核苷酸变异非常罕见,通常与治疗药物的药代动力学变化有关。最近,一种非同义变体(野生型CAR中的F243S)与影响神经发育的Kleefstra综合征(MIM 610253)有关。我们在患有克利夫特拉样症状的患者中发现了另一种以前未知的CAR变体(I281T)。详细的报告基因分析和分子模型表明,I281T突变降低了CAR招募共激活剂的能力,可能是通过干扰功能性CAR/类视黄醛X受体(RXR)异源二聚体的组装。尽管I281T变异似乎不会导致患者的这些特征,但目前的研究增加了我们对CAR功能的了解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Functional Characterization of a Novel Variant of the Constitutive Androstane Receptor (CAR, NR1I3)
The nuclear receptor constitutive androstane receptor (CAR; NR1I3) controls the inducible expression of many enzymes and transporters involved in drug metabolism and transport, energy metabolism and toxicity. Single nucleotide variants of CAR are quite rare and usually associated with changes in pharmacokinetics of therapeutic drugs. Recently, a non-synonymous variant (F243S in the wild-type CAR) has been linked to the Kleefstra syndrome (MIM 610253) affecting neurological development. We identified another, previously unknown CAR variant (I281T) in a patient suffering from Kleefstra-like symptoms. Detailed reporter gene assays and molecular modelling indicated that the I281T mutation decreases the ability of CAR to recruit co-activators, likely by interfering with the assembly of functional CAR/retinoid X receptor (RXR) heterodimers. Although the I281T variant does not seem to cause the features of the patient, the present study adds to our knowledge about CAR function.
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