ACS Chem Biol. 2021 Jul 16;16(7):1159-1163. doi: 10.1021/acschembio.1c00326. Epub 2021 Jun 24.
The nuclear receptor-related 1 protein, Nurr1, is a transcription factor critical for the development and maintenance of dopamine-producing neurons in the substantia nigra pars compacta, a cell population that progressively loses the ability to make dopamine and degenerates in Parkinson's disease. Recently, we demonstrated that Nurr1 binds directly to and is regulated by the endogenous dopamine metabolite 5,6-dihydroxyindole (DHI). Unfortunately, DHI is an unstable compound, and thus a poor tool for studying Nurr1 function. Here, we report that 5-chloroindole, an unreactive analog of DHI, binds directly to the Nurr1 ligand binding domain with micromolar affinity and stimulates the activity of Nurr1, including the transcription of genes governing the synthesis and packaging of dopamine.
核受体相关蛋白 1(Nurr1)是一种转录因子,对于中脑黑质致密部多巴胺能神经元的发育和维持至关重要,而多巴胺能神经元会逐渐丧失产生多巴胺的能力并在帕金森病中退化。最近,我们证明 Nurr1 可直接与内源性多巴胺代谢物 5,6-二羟基吲哚(DHI)结合,并受其调控。遗憾的是,DHI 是一种不稳定的化合物,因此不太适合用于研究 Nurr1 功能。在这里,我们报告 5-氯吲哚是 DHI 的一种无反应性类似物,可与 Nurr1 的配体结合域以微摩尔亲和力直接结合,并刺激 Nurr1 的活性,包括调节多巴胺合成和包装的基因的转录。