Localization of DJ-1 mRNA in the mouse brain

被引:38
作者
Shang, H
Lang, D
Jean-Marc, B
Kaelin-Lang, A [1 ]
机构
[1] Univ Bern, Inselspital, Neuromorphol Lab, Dept Neurol, CH-3010 Bern, Switzerland
[2] Sichuan Univ, W China Hosp, Dept Neurol, Chengdu 610041, SiChuan, Peoples R China
[3] Univ Zurich, Childrens Hosp, Div Oncol, Neuro Oncol Program, CH-8032 Zurich, Switzerland
[4] Natl Univ Singapore, Dept Med, Singapore 119074, Singapore
关键词
DJ-1; gene; Parkinson's disease; in situ hybridization; central nervous system;
D O I
10.1016/j.neulet.2004.06.002
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
DJ-1 is mutated in autosomal recessive, early onset Parkinson's disease but the exact localization of the DJ-1 gene product in the mammalian brain is largely unknown. We aimed to evaluate the DJ-1 mRNA expression pattern in the mouse brain. Serial coronal sections of brains of five male and five female adult mice were investigated by using in situ hybridization with a DJ-1 specific S-35-labeled oligonucleotide probe. Hybridized sections were analyzed after exposure to autoradiography films and after coating with a photographic emulsion. DJ-1 was heterogeneously expressed throughout the mouse central nervous system. A high expression of DJ-1 mRNA was detected in neuronal and non-neuronal populations of several structures of the motor system such as the substantia nigra, the red nucleus, the caudate putamen, the globus pallidus, and the deep nuclei of the cerebellum. Furthermore, DJ-1 mRNA was also highly expressed in non-motor structures including the hippocampus, the olfactory bulb, the reticular nucleus of the thalamus, and the piriform cortex. The high expression of DJ-1 mRNA in brain regions involved in motor control is compatible with the occurrence of parkinsonian symptoms after DJ-1 mutations. However, expression in other regions indicates that a dysfunction of DJ-1 may contribute to additional clinical features in patients with a DJ-1 mutation. (C) 2004 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:273 / 277
页数:5
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