Homeobox gene Pitx3 and its role in the development of dopamine neurons of the substantia nigra

被引:103
作者
Smidt, MP [1 ]
Smits, SM [1 ]
Burbach, JPH [1 ]
机构
[1] Univ Utrecht, Dept Pharmacol & Anat, Rudolf Magnus Inst Neurosci, NL-3584 CG Utrecht, Netherlands
关键词
embryonic development; midbrain; aphakia mouse mutant; striatal connectivity; behavior;
D O I
10.1007/s00441-004-0943-1
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The homeobox gene Pitx3 plays an important part in the development and function of vertebrate midbrain dopaminergic neurons. Re-localization of the genetic defect in the mouse mutant aphakia to the Pitx3 locus, together with the subsequent identification of two deletions causing the gene to be silent, has been the hallmark of several studies into the role of Pitx3. In this review, we summarize the data and reflect on the role of Pitx3 in the development of dopamine neurons in the midbrain. The data indicate that Pitx3 is essential for the survival of dopamine neurons located in the substantia nigra compacta during development. Molecular analysis of the underlying mechanisms might provide new insights for understanding the selective degeneration observed in Parkinson patients.
引用
收藏
页码:35 / 43
页数:9
相关论文
共 59 条
[31]   ISTHMIC ORIGIN OF NEURONS OF THE RAT SUBSTANTIA-NIGRA [J].
MARCHAND, R ;
POIRIER, LJ .
NEUROSCIENCE, 1983, 9 (02) :373-381
[32]  
Marcos C, 1996, Int J Dev Biol, VSuppl 1, p137S
[33]   NEUROTRANSMITTER ORGANIZATION AND CONNECTIVITY OF THE BASAL GANGLIA IN VERTEBRATES - IMPLICATIONS FOR THE EVOLUTION OF BASAL GANGLIA [J].
MEDINA, L ;
REINER, A .
BRAIN BEHAVIOR AND EVOLUTION, 1995, 46 (4-5) :235-258
[34]   Pitx3 is required for development of substantia nigra dopaminergic neurons [J].
Nunes, I ;
Tovmasian, LT ;
Silva, RM ;
Burke, RE ;
Goff, SP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (07) :4245-4250
[35]   A double-deletion mutation in the Pitx3 gene causes arrested lens development in aphakia mice [J].
Rieger, DK ;
Reichenberger, E ;
McLean, W ;
Sidow, A ;
Olsen, BR .
GENOMICS, 2001, 72 (01) :61-72
[36]   Nurr1 is essential for the induction of the dopaminergic phenotype and the survival of ventral mesencephalic late dopaminergic precursor neurons [J].
Saucedo-Cardenas, O ;
Quintana-Hau, JD ;
Le, WD ;
Smidt, MP ;
Cox, JJ ;
DeMayo, F ;
Burbach, JPH ;
Conneely, OM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (07) :4013-4018
[37]   Deletion in the promoter region and altered expression of Pitx3 homeobox gene in aphakia mice [J].
Semina, EV ;
Murray, JC ;
Reiter, R ;
Hrstka, RF ;
Graw, J .
HUMAN MOLECULAR GENETICS, 2000, 9 (11) :1575-1585
[38]   Isolation of a new homeobox gene belonging to the Pitx/Rieg family: Expression during lens development and mapping to the aphakia region on mouse chromosome 19 [J].
Semina, EV ;
Reiter, RS ;
Murray, JC .
HUMAN MOLECULAR GENETICS, 1997, 6 (12) :2109-2116
[39]   A novel homeobox gene PITX3 is mutated in families with autosomal-dominant cataracts and ASMD [J].
Semina, EV ;
Ferrell, RE ;
Mintz-Hittner, HA ;
Bitoun, P ;
Alward, WLM ;
Reiter, RS ;
Funkhauser, C ;
Daack-Hirsch, S ;
Murray, JC .
NATURE GENETICS, 1998, 19 (02) :167-170
[40]   Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndrome [J].
Semina, EV ;
Reiter, R ;
Leysens, NJ ;
Alward, WLM ;
Small, KW ;
Datson, NA ;
SiegelBartelt, J ;
BierkeNelson, D ;
Bitoun, P ;
Zabel, BU ;
Carey, JC ;
Murray, JC .
NATURE GENETICS, 1996, 14 (04) :392-399