Literature DB >> 12124430

Dynamics of tyrosine hydroxylase promoter activity during midbrain dopaminergic neuron development.

Natsuki Matsushita1, Hideki Okada, Yasunobu Yasoshima, Kazuaki Takahashi, Kazutoshi Kiuchi, Kazuto Kobayashi.   

Abstract

Dopamine (DA)-producing neurons in the ventral midbrain are generated from a specified neuronal lineage and form selective axonal pathways that mediate multiple CNS functions. Expression of the gene encoding tyrosine hydroxylase (TH), which is a key enzyme of catecholamine biosynthesis, is regulated during the development of midbrain DA neurons. In the present study, we report the developmental regulation and cell type specificity of TH gene promoter in the ventral midbrain by using a green fluorescent protein (GFP) reporter system. Transgenic mice were generated that express GFP in the majority of midbrain DA neurons under the control of the 9-kb upstream region of the rat TH gene. At an early embryonic stage, GFP expression was induced in the developing DA neurons, and the expression was then markedly down-regulated at later embryonic stages. However, the expression was reactivated and approached the adult levels during early post-natal development. These developmental changes in GFP expression patterns suggest the presence of multistep regulatory mechanisms for TH gene expression during DA neuron development. The TH promoter appears to possess transcriptional elements at least necessary for the induction of TH expression at the early embryonic stage and its reactivation during the post-natal development.

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Year:  2002        PMID: 12124430     DOI: 10.1046/j.1471-4159.2002.00972.x

Source DB:  PubMed          Journal:  J Neurochem        ISSN: 0022-3042            Impact factor:   5.372


  80 in total

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5.  Cortical and striatal expression of tyrosine hydroxylase mRNA in neonatal and adult mice.

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10.  Effects of acute and chronic nicotine on catecholamine neurons of the nucleus of the solitary tract.

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Journal:  Am J Physiol Regul Integr Comp Physiol       Date:  2018-10-24       Impact factor: 3.619

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