Early developmental failure of substantia nigra dopamine neurons in mice lacking the homeodomain gene Pitx3
Author:
Smidt Marten P.1, Smits Simone M.1, Bouwmeester Hans1, Hamers Frank P. T.1, van der Linden Annemarie J. A.1, Hellemons Anita J. C. G. M.1, Graw Jochen2, Burbach J. Peter H.1
Affiliation:
1. Rudolf Magnus Institute of Neuroscience, Department of Pharmacology and Anatomy, University Medical Center, Universiteitsweg 100, 3584 CG Utrecht, The Netherlands 2. GSF, Institute of Developmental Genetics, Ingolstaedter Landstrasse 1, D-85764 München, Germany
Abstract
The mesencephalic dopamine (mesDA) system is involved in the control of movement and behavior. The expression of Pitx3 in the brain is restricted to the mesDA system and the gene is induced relatively late, at E11.5, a time when tyrosine hydroxylase (Th) gene expression is initiated. We show here that, in the Pitx3-deficient aphakia(ak) mouse mutant, the mesDA system is malformed. Owing to the developmental failure of mesDA neurons in the lateral field of the midbrain,mesDA neurons are not found in the SNc and the projections to the caudate putamen are selectively lost. However, Pitx3 is expressed in all mesDA neurons in control animals. Therefore, mesDA neurons react specifically to the loss of Pitx3. Defects of motor control where not seen in the ak mice,suggesting that other neuronal systems compensate for the absence of the nigrostriatal pathway. However, an overall lower activity was observed. The results suggest that Pitx3 is specifically required for the formation of the SNc subfield at the onset of dopaminergic neuron differentiation.
Publisher
The Company of Biologists
Subject
Developmental Biology,Molecular Biology
Reference51 articles.
1. Burbach, J. P. H., Smits, S. and Smidt, M. P.(2003). Transcription factors in the development of midbrain dopamine neurons. Ann. New York Acad. Sci.991, 61-69. 2. Cazorla, P., Smidt, M. P., O'Malley, K. L. and Burbach, J. P. H. (2000). A response element for the homeodomain transcription factor Ptx3 in the tyrosine hydroxylase gene promoter. J. Neurochem.74,1829-1837. 3. Chen, H., Ovchinnikov, D., Pressman, C. L., Aulehla, A., Lun, Y. and Johnson, R. L. (1998a). Multiple calvarial defects in Lmx1b mutant mice. Dev. Genet.22,314-320. 4. Chen, H., Lun, Y., Ovchinnikov, D., Kokubo, H., Oberg, K. C.,Pepicelli, C. V., Gan, L., Lee, B. and Johnson, R. L.(1998b). Limb and kidney defects in Lmx1b mutant mice suggest an involvement of LMX1B in human nail patella syndrome. Nat. Genet.19,51-55. 5. Cooper, J. R., Bloom, F. E. and Roth, R. H.(1977). The Biochemical Basis of Neuropharmacology. New York: Oxford University Press.
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