Genome wide expression profiling of the mesodiencephalic region identifies novel factors involved in early and late dopaminergic development

被引:35
作者
Chakrabarty, Koushik [1 ]
Von Oerthel, Lars [1 ,2 ]
Hellemons, Anita [1 ]
Clotman, Frederic [3 ]
Espana, Agnes [3 ]
Koerkamp, Marian Groot [4 ]
Holstege, Frank C. P. [4 ]
Pasterkamp, R. Jeroen [1 ]
Smidt, Marten P. [1 ,2 ]
机构
[1] Univ Med Ctr Utrecht, Rudolf Magnus Inst Neurosci, Dept Neurosci & Pharmacol, NL-3584 CG Utrecht, Netherlands
[2] Univ Amsterdam, Swammerdam Inst Life Sci, NL-1098 XH Amsterdam, Netherlands
[3] Catholic Univ Louvain, Inst Neurosci, Lab Neural Differentiat, B-1200 Brussels, Belgium
[4] UMC Utrecht, Microarray Facil, NL-3508 AB Utrecht, Netherlands
关键词
Neuronal; Development; Onecut; Pitx3; Nurr1;
D O I
10.1242/bio.20121230
中图分类号
Q [生物科学];
学科分类号
090105 [作物生产系统与生态工程];
摘要
Meso-diencephalic dopaminergic (mdDA) neurons are critical for motor control and cognitive functioning and their loss or dysfunction is associated with disorders such as Parkinson's disease (PD), schizophrenia and addiction. However, relatively little is known about the molecular mechanisms underlying mdDA neuron development and maintenance. Here, we determined the spatiotemporal map of genes involved in the development of mdDA neurons to gain further insight into their molecular programming. Genome-wide gene expression profiles of the developing ventral mesencephalon (VM) were compared at different developmental stages leading to the identification of novel regulatory roles of neuronal signaling through nicotinic acthylcholine receptors (Chrna6 and Chrnb3 subunits) and the identification of novel transcription factors (Oc2 and 3) involved in the generation of the mdDA neuronal field. We show here that Pitx3, in cooperation with Nurr1, is the critical component in the activation of the Chrna6 and Chrnb3 subunits in mdDA neurons. Furthermore, we provide evidence of two divergent regulatory pathways resulting in the expression of Chrna6 and Chrnb3 respectively. (C) 2012. Published by The Company of Biologists Ltd.
引用
收藏
页码:693 / 704
页数:12
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