Dermentzaki Georgia, Paschalidis Nikolaos, Politis Panagiotis K, Stefanis Leonidas
From the Biomedical Research Foundation of the Academy of Athens, Athens 11527 and.
From the Biomedical Research Foundation of the Academy of Athens, Athens 11527 and the Second Department of Neurology, National and Kapodistrian University of Athens Medical School, Hospital Attikon, Athens 12462, Greece,
J Biol Chem. 2016 Apr 15;291(16):8756-72. doi: 10.1074/jbc.M115.704973. Epub 2016 Feb 23.
α-Synuclein, a presynaptic neuronal protein encoded by the SNCA gene, is strongly implicated in Parkinson disease (PD). PD pathogenesis is linked to increased SNCA levels; however, the transcriptional elements that control SNCA expression are still elusive. Previous experiments in PC12 cells demonstrated that the transcription factor zinc finger and SCAN domain containing 21 (ZSCAN21) plays an important regulatory role in SNCA transcription. Currently, we characterized the role of ZSCAN21 in SNCA transcription in primary neuronal cultures and in vivo We found that ZSCAN21 is developmentally expressed in neurons in different rat brain regions. We confirmed its binding in the intron 1 region of SNCA in rat cortical cultures. Lentivirus-mediated silencing of ZSCAN21 increased significantly SNCA promoter activity, mRNA, and protein levels in such cultures. In contrast, ZSCAN21 silencing reduced SNCA in neurosphere cultures. Interestingly, ZSCAN21 overexpression in cortical neurons led to robust mRNA but negligible protein expression, suggesting that ZSCAN21 protein levels are tightly regulated post-transcriptionally and/or post-translationally in primary neurons. Efficient adeno-associated virus-mediated knockdown of ZSCAN21 in the postnatal and adult hippocampus, an area linked with non-motor PD symptoms, revealed no significant alterations in SNCA levels. Overall, our study demonstrates that ZSCAN21 is involved in the transcriptional regulation of SNCA in primary neuronal cultures, but the direction of the effect is variable, likely depending on neuronal maturation. However, the unaltered SNCA levels observed following ZSCAN21 down-regulation in the rat brain, possibly due to compensatory mechanisms, imply that ZSCAN21 is not a master regulator of SNCA in vivo.
α-突触核蛋白是一种由SNCA基因编码的突触前神经元蛋白,与帕金森病(PD)密切相关。PD的发病机制与SNCA水平升高有关;然而,控制SNCA表达的转录元件仍不清楚。先前在PC12细胞中的实验表明,转录因子含锌指和SCAN结构域21(ZSCAN21)在SNCA转录中起重要调节作用。目前,我们在原代神经元培养物和体内表征了ZSCAN21在SNCA转录中的作用。我们发现ZSCAN21在大鼠不同脑区的神经元中呈发育性表达。我们在大鼠皮质培养物中证实了它与SNCA内含子1区域的结合。慢病毒介导的ZSCAN21沉默显著增加了此类培养物中SNCA启动子活性、mRNA和蛋白水平。相反,ZSCAN21沉默降低了神经球培养物中的SNCA。有趣的是,皮质神经元中ZSCAN21的过表达导致强大的mRNA表达,但蛋白表达可忽略不计,这表明ZSCAN21蛋白水平在原代神经元中受到转录后和/或翻译后严格调控。在出生后和成年海马体(与非运动性PD症状相关的区域)中,腺相关病毒介导的ZSCAN21有效敲低显示SNCA水平无显著变化。总体而言,我们的研究表明ZSCAN21参与原代神经元培养物中SNCA的转录调控,但作用方向是可变的,可能取决于神经元成熟度。然而,在大鼠脑中ZSCAN21下调后观察到的SNCA水平未改变,可能是由于补偿机制,这意味着ZSCAN21在体内不是SNCA的主要调节因子。