Lmx1a is an activator of Rgs4 and Gbr10 and is responsible for the correct specification of rostral and medial mdDA neurons
Autor: | Frank C. P. Holstege, Gerard Scheppink, Marian J.A. Groot-Koerkamp, Lars von Oerthel, Raymond D. Schellevis, Lars P. van der Heide, Elisa J. Hoekstra, Marten P. Smidt, Annemarie J. A. van der Linden |
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Přispěvatelé: | Molecular Neuroscience (SILS, FNWI) |
Jazyk: | angličtina |
Rok vydání: | 2013 |
Předmět: |
Transcription
Genetic GRB10 Adaptor Protein LIM-Homeodomain Proteins Biology Cell Line Mice Dopamine Dopaminergic Cell medicine Animals Transcription factor Oligonucleotide Array Sequence Analysis Microarray analysis techniques Activator (genetics) Dopaminergic Neurons Gene Expression Profiling General Neuroscience Dopaminergic Brain Gene Expression Regulation Developmental Molecular biology Mice Mutant Strains Cell biology Mice Inbred C57BL Vesicular Monoamine Transport Proteins Mutation Homeobox Stem cell RGS Proteins Transcription Factors medicine.drug |
Zdroj: | European Journal of Neuroscience, 37(1), 23-32. Wiley-Blackwell |
ISSN: | 1460-9568 0953-816X |
DOI: | 10.1111/ejn.12022 |
Popis: | The LIM homeodomain transcription factor Lmx1a is a very potent inducer of stem cells towards dopaminergic neurons. Despite several studies on the function of this gene, the exact in vivo role of Lmx1a in mesodiencephalic dopamine (mdDA) neuronal specification is still not understood. To analyse the genes functioning downstream of Lmx1a, we performed expression microarray analysis of LMX1A-overexpressing MN9D dopaminergic cells. Several interesting regulated genes were identified, based on their regulation in other previously generated expression arrays and on their expression pattern in the developing mdDA neuronal field. Post analysis through in vivo expression analysis in Lmx1a mouse mutant (dr/dr) embryos demonstrated a clear decrease in expression of the genes Grb10 and Rgs4, in and adjacent to the rostral and dorsal mdDA neuronal field and within the Lmx1a expression domain. Interestingly, the DA marker Vmat2 was significantly up-regulated as a consequence of increased LMX1A dose, and subsequent analysis on Lmx1a-mutant E14.5 and adult tissue revealed a significant decrease in Vmat2 expression in mdDA neurons. Taken together, microarray analysis of an LMX1A-overexpression cell system resulted in the identification of novel direct or indirect downstream targets of Lmx1a in mdDA neurons: Grb10, Rgs4 and Vmat2. |
Databáze: | OpenAIRE |
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