Arx acts as a regional key selector gene in the ventral telencephalon mainly through its transcriptional repression activity

被引:41
作者
Colasante, Gaia
Sessa, Alessandro
Crispi, Stefania [2 ]
Calogero, Raffaele [3 ]
Mansouri, Ahmed [4 ]
Collombat, Patrick [5 ]
Broccoli, Vania [1 ]
机构
[1] Ist Sci San Raffaele, Dev Neuropathol Lab, Stem Cell & Neurogenesis Unit, Div Neurosci, I-20132 Milan, Italy
[2] IGB CNR, Human Mol Genet Lab, I-80131 Naples, Italy
[3] Univ Turin, Dept Clin & Biol Sci, Turin, Italy
[4] Max Planck Inst Biophys Chem, Dept Mol Cell Biol, D-37077 Gottingen, Germany
[5] Fac Sci, Mouse Mol Genet Dept, INSERM, U636, F-06108 Nice, France
关键词
Forebrain; Telencephalon; Basal ganglia; Neurogenesis; GABA; Cell migration; Arx; Lissencephaly; West syndrome; Gene expression; Expression profile; Transcription factor; FOREBRAIN CHOLINERGIC NEURONS; LINKED MENTAL-RETARDATION; PRADER-WILLI-SYNDROME; HOMEOBOX GENE; GABAERGIC INTERNEURONS; TANGENTIAL MIGRATION; ABNORMAL GENITALIA; CEREBRAL-CORTEX; DLX GENES; ENDOCRINE PANCREAS;
D O I
10.1016/j.ydbio.2009.07.014
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The homeobox-containing gene Arx is expressed during ventral telencephalon development and required for correct GABAergic interneuron tangential migration from the ganglionic eminences to the olfactory bulbs, cerebral cortex and striatum. Its human ortholog is associated with a variety of neurological clinical manifestations whose symptoms are compatible with the loss of cortical interneurons and altered basal ganglia-related activities. Herein, we report the identification of a number of genes whose expression is consistently altered in Arx mutant ganglionic eminences. Our analyses revealed a striking ectopic expression in the ganglionic eminences of several of these genes normally at most marginally expressed in the ventral telencephalon. Among them, Ebf3 was functionally analyzed. Thus, its ectopic expression in ventral telencephalon was found to prevent neuronal tangential migration. Further, we showed that Arx is sufficient to repress Ebf3 endogenous expression and that its silencing in Arx mutant tissues partially rescues tangential cell movement. Together, these data provide new insights into the molecular pathways regulated by Arx during telencephalon development. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:59 / 71
页数:13
相关论文
共 80 条
[1]   Crossveinless-2 is a BMP feedback inhibitor that binds Chordin/BMP to regulate Xenopus embryonic patterning [J].
Ambrosio, Andrea L. ;
Taelman, Vincent F. ;
Lee, Hojoon X. ;
Metzinger, Carrie A. ;
Coffinier, Catherine ;
De Robertis, E. M. .
DEVELOPMENTAL CELL, 2008, 15 (02) :248-260
[2]   Mutations of the homeobox genes Dlx-1 and Dlx-2 disrupt the striatal subventricular zone and differentiation of late born striatal neurons [J].
Anderson, SA ;
Qiu, MS ;
Bulfone, A ;
Eisenstat, DD ;
Meneses, J ;
Pedersen, R ;
Rubenstein, JLR .
NEURON, 1997, 19 (01) :27-37
[3]  
[Anonymous], 1993, Resampling-Based Multiple Testing: Examples and Methods for p-Value Adjustment
[4]   ARX, a novel Prd-class-homeobox gene highly expressed in the telencephalon, is mutated in X-linked mental retardation [J].
Bienvenu, T ;
Poirier, K ;
Friocourt, G ;
Bahi, N ;
Beaumont, D ;
Fauchereau, F ;
Ben Jeema, L ;
Zemni, R ;
Vinet, MC ;
Francis, F ;
Couvert, P ;
Gomot, M ;
Moraine, C ;
van Bokhoven, H ;
Kalscheuer, V ;
Frints, S ;
Gecz, J ;
Ohzaki, K ;
Chaabouni, H ;
Fryns, JP ;
Desportes, V ;
Beldjord, C ;
Chelly, J .
HUMAN MOLECULAR GENETICS, 2002, 11 (08) :981-991
[5]   Inactivation of the mouse Magel2 gene results in growth abnormalities similar to Prader-Willi syndrome [J].
Bischof, Jocelyn M. ;
Stewart, Colin L. ;
Wevrick, Rachel .
HUMAN MOLECULAR GENETICS, 2007, 16 (22) :2713-2719
[6]   Meninges control tangential migration of hem-derived Cajal-Retzius cells via CXCL12/CXCR4 signaling [J].
Borrell, Victor ;
Marin, Oscar .
NATURE NEUROSCIENCE, 2006, 9 (10) :1284-1293
[7]   Dmbx1 is a paired-box containing gene specifically expressed in the caudal most brain structures [J].
Broccoli, V ;
Colombo, E ;
Cossu, G .
MECHANISMS OF DEVELOPMENT, 2002, 114 (1-2) :219-223
[8]   Dynamic spatiotemporal expression of LIM genes and cofactors in the embryonic and postnatal cerebral cortex [J].
Bulchand, S ;
Subramanlan, L ;
Tole, S .
DEVELOPMENTAL DYNAMICS, 2003, 226 (03) :460-469
[9]   Proneural bHLH and Brn proteins coregulate a neurogenic program through cooperative binding to a conserved DNA motif [J].
Castro, Diogo S. ;
Skowronska-Krawczyk, Dorota ;
Armant, Olivier ;
Donaldson, Ian J. ;
Parras, Carlos ;
Hunt, Charles ;
Critchley, James A. ;
Nguyen, Laurent ;
Gossler, Achim ;
Goettgens, Berthold ;
Matter, Jean-Marc ;
Guillemot, Francois .
DEVELOPMENTAL CELL, 2006, 11 (06) :831-844
[10]   Mice lacking Dlx1 show subtype-specific loss of interneurons, reduced inhibition and epilepsy [J].
Cobos, I ;
Calcagnotto, ME ;
Vilaythong, AJ ;
Thwin, MT ;
Noebels, JL ;
Baraban, SC ;
Rubenstein, JLR .
NATURE NEUROSCIENCE, 2005, 8 (08) :1059-1068