Please use this identifier to cite or link to this item: https://doi.org/10.1016/j.neulet.2004.06.002
DC FieldValue
dc.titleLocalization of DJ-1 mRNA in the mouse brain
dc.contributor.authorShang, H.
dc.contributor.authorLang, D.
dc.contributor.authorJean-Marc, B.
dc.contributor.authorKaelin-Lang, A.
dc.date.accessioned2016-11-28T10:14:19Z
dc.date.available2016-11-28T10:14:19Z
dc.date.issued2004-09-09
dc.identifier.citationShang, H., Lang, D., Jean-Marc, B., Kaelin-Lang, A. (2004-09-09). Localization of DJ-1 mRNA in the mouse brain. Neuroscience Letters 367 (3) : 273-277. ScholarBank@NUS Repository. https://doi.org/10.1016/j.neulet.2004.06.002
dc.identifier.issn03043940
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/130931
dc.description.abstractDJ-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 35S-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. © 2004 Elsevier Ireland Ltd. All rights reserved.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1016/j.neulet.2004.06.002
dc.sourceScopus
dc.subjectBasal ganglia, cortex, cerebellum
dc.subjectCentral nervous system
dc.subjectDJ-1 gene
dc.subjectIn situ hybridization
dc.subjectMotor systems and sensorimotor integration
dc.subjectParkinson's disease
dc.typeArticle
dc.contributor.departmentMEDICINE
dc.description.doi10.1016/j.neulet.2004.06.002
dc.description.sourcetitleNeuroscience Letters
dc.description.volume367
dc.description.issue3
dc.description.page273-277
dc.description.codenNELED
dc.identifier.isiut000223967500002
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