Hwang Dong-Youn, Hong Sunghoi, Jeong Joo-Won, Choi Sangdun, Kim Hansoo, Kim Jangwoo, Kim Kwang-Soo
Molecular Neurobiology Laboratory, McLean Hospital and Harvard Medical School, Belmont, MA, USA.
J Neurochem. 2009 Dec;111(5):1202-12. doi: 10.1111/j.1471-4159.2009.06404.x. Epub 2009 Sep 24.
Midbrain dopamine (mDA) neurons play critical roles in the regulation of voluntary movement and their dysfunction is associated with Parkinson's disease. Pitx3 has been implicated in the proper development of mDA neurons in the substantia nigra pars compacta, which are selectively lost in Parkinson's disease. However, the basic mechanisms underlying its role in mDA neuron development and/or survival are poorly understood. Toward this goal, we sought to identify downstream target genes of Pitx3 by comparing gene expression profiles in mDA neurons of wild-type and Pitx3-deficient aphakia mice. This global gene expression analysis revealed many potential target genes of Pitx3; in particular, the expression of vesicular monoamine transporter 2 and dopamine transporter, responsible for dopamine storage and reuptake, respectively, is greatly reduced in mDA neurons by Pitx3 ablation. In addition, gain-of-function analyses and chromatin immunoprecipitation strongly indicate that Pitx3 may directly activate transcription of vesicular monoamine transporter 2 and dopamine transporter genes, critically contributing to neurotransmission and/or survival of mDA neurons. As the two genes have been known to be regulated by Nurr1, another key dopaminergic transcription factor, we propose that Pitx3 and Nurr1 may coordinately regulate mDA specification and survival, at least in part, through a merging and overlapping downstream pathway.
中脑多巴胺(mDA)神经元在自主运动调节中起关键作用,其功能障碍与帕金森病相关。Pitx3与黑质致密部mDA神经元的正常发育有关,而这些神经元在帕金森病中会选择性丧失。然而,其在mDA神经元发育和/或存活中作用的基本机制仍知之甚少。为实现这一目标,我们试图通过比较野生型和Pitx3缺陷无晶状体小鼠的mDA神经元中的基因表达谱,来鉴定Pitx3的下游靶基因。这种全基因组表达分析揭示了许多Pitx3的潜在靶基因;特别是,分别负责多巴胺储存和再摄取的囊泡单胺转运体2和多巴胺转运体的表达,在mDA神经元中因Pitx3缺失而大幅降低。此外,功能获得分析和染色质免疫沉淀强烈表明,Pitx3可能直接激活囊泡单胺转运体2和多巴胺转运体基因的转录,对mDA神经元的神经传递和/或存活起关键作用。由于已知这两个基因受另一个关键的多巴胺能转录因子Nurr1调控,我们提出Pitx3和Nurr1可能至少部分通过合并和重叠的下游途径协同调节mDA的特化和存活。