De Gois Stéphanie, Slama Patrick, Pietrancosta Nicolas, Erdozain Amaia M, Louis Franck, Bouvrais-Veret Caroline, Daviet Laurent, Giros Bruno
INSERM U952, 75005 Paris, France; CNRS UMR 7224, 75005 Paris, France; Université Pierre et Marie Curie, Neuroscience Paris Seine, 75005 Paris, France; Douglas Hospital Research Center, Department of Psychiatry, McGill University, Montreal H4H 1R3 Quebec, Canada.
INSERM U952, 75005 Paris, France; CNRS UMR 7224, 75005 Paris, France; Université Pierre et Marie Curie, Neuroscience Paris Seine, 75005 Paris, France.
J Biol Chem. 2015 Jul 17;290(29):17848-17862. doi: 10.1074/jbc.M115.646315. Epub 2015 Jun 5.
Dopamine (DA) is a major regulator of sensorimotor and cognitive functions. The DA transporter (DAT) is the key protein that regulates the spatial and temporal activity of DA release into the synaptic cleft via the rapid reuptake of DA into presynaptic termini. Several lines of evidence have suggested that transporter-interacting proteins may play a role in DAT function and regulation. Here, we identified the tetratricopeptide repeat domain-containing protein Ctr9 as a novel DAT binding partner using a yeast two-hybrid system. We showed that Ctr9 is expressed in dopaminergic neurons and forms a stable complex with DAT in vivo via GST pulldown and co-immunoprecipitation assays. In mammalian cells co-expressing both proteins, Ctr9 partially colocalizes with DAT at the plasma membrane. This interaction between DAT and Ctr9 results in a dramatic enhancement of DAT-mediated DA uptake due to an increased number of DAT transporters at the plasma membrane. We determined that the binding of Ctr9 to DAT requires residues YKF in the first half of the DAT C terminus. In addition, we characterized Ctr9, providing new insight into this protein. Using three-dimensional modeling, we identified three novel tetratricopeptide repeat domains in the Ctr9 sequence, and based on deletion mutation experiments, we demonstrated the role of the SH2 domain of Ctr9 in nuclear localization. Our results demonstrate that Ctr9 localization is not restricted to the nucleus, as previously described for the transcription complex Paf1. Taken together, our data provide evidence that Ctr9 modulates DAT function by regulating its trafficking.
多巴胺(DA)是感觉运动和认知功能的主要调节因子。多巴胺转运体(DAT)是一种关键蛋白,它通过将多巴胺快速重新摄取到突触前终末来调节多巴胺释放到突触间隙中的空间和时间活性。多条证据表明,与转运体相互作用的蛋白可能在DAT功能和调节中发挥作用。在这里,我们使用酵母双杂交系统鉴定了含四肽重复结构域的蛋白Ctr9作为一种新的DAT结合伴侣。我们通过谷胱甘肽S-转移酶下拉实验和免疫共沉淀实验表明,Ctr9在多巴胺能神经元中表达,并在体内与DAT形成稳定复合物。在共表达这两种蛋白的哺乳动物细胞中,Ctr9在质膜上与DAT部分共定位。DAT与Ctr9之间的这种相互作用导致质膜上DAT转运体数量增加,从而显著增强了DAT介导的多巴胺摄取。我们确定Ctr9与DAT的结合需要DAT C末端前半部分的YKF残基。此外,我们对Ctr9进行了表征,为该蛋白提供了新的见解。通过三维建模,我们在Ctr9序列中鉴定了三个新的四肽重复结构域,并基于缺失突变实验,证明了Ctr9的SH2结构域在核定位中的作用。我们的结果表明,Ctr9的定位并不局限于细胞核,这与之前描述的转录复合物Paf1不同。综上所述,我们的数据提供了证据,表明Ctr9通过调节DAT的运输来调节其功能。