Thuret Sandrine, Bhatt Lavinia, O'Leary Dennis D M, Simon Horst H
Department of Anatomy and Cell Biology III, University of Heidelberg, 69120 Heidelberg, Germany.
Mol Cell Neurosci. 2004 Mar;25(3):394-405. doi: 10.1016/j.mcn.2003.11.004.
The hallmark of Parkinson's Disease is the degenerative loss of mesencephalic dopaminergic (mDA) neurons. Previous studies have shown that the homeobox transcription factors, engrailed-1 and -2, are essential for the survival of these cells. To identify genes downstream of engrailed-1 and -2, we performed a PCR-based differential display, comparing RNA from engrailed-1/2 double mutant and wild type ventral midbrain of different embryonic ages to adult olfactory bulb, a source of unrelated DA neurons. Here, we report the result of this experiment and describe the developmental expression pattern in the ventral midbrain of three of the isolated genes, HNF3alpha, synaptotagmin I, and Ebf3. Though not regulated by engrailed-1 and -2, the expression of all three genes is limited to mDA neurons and a few other brain areas. HNF3alpha appears in the precursors of mDA neurons at E9 and is expressed in the adult brain almost exclusively by this neuronal population. Synaptotagmin I is expressed from E14 into adulthood. Ebf3, in contrast, is transiently expressed during early postmitotic differentiation.
帕金森病的标志是中脑多巴胺能(mDA)神经元的退行性丧失。先前的研究表明,同源盒转录因子 engrailed-1 和 -2 对这些细胞的存活至关重要。为了鉴定 engrailed-1 和 -2 下游的基因,我们进行了基于 PCR 的差异显示,将不同胚胎期 engrailed-1/2 双突变体和野生型腹侧中脑的 RNA 与成年嗅球(一种不相关的 DA 神经元来源)进行比较。在此,我们报告该实验的结果,并描述分离出的三个基因 HNF3α、突触结合蛋白 I 和 Ebf3 在腹侧中脑的发育表达模式。尽管这三个基因不受 engrailed-1 和 -2 的调控,但其表达均局限于 mDA 神经元和其他一些脑区。HNF3α 在胚胎第 9 天出现在 mDA 神经元的前体细胞中,在成年大脑中几乎仅由该神经元群体表达。突触结合蛋白 I 从胚胎第 14 天开始表达直至成年。相比之下,Ebf3 在有丝分裂后早期分化过程中短暂表达。