Zic1 LEVELS REGULATE MOSSY FIBER NEURON POSITION AND AXON LATERALITY CHOICE IN THE VENTRAL BRAIN STEM

被引:17
作者
Dipietrantonio, H. J. [1 ]
Dymecki, S. M. [1 ]
机构
[1] Harvard Univ, Sch Med, Dept Genet, Boston, MA 02115 USA
关键词
pontocerebellar circuitry; precerebellar mossy fiber afferents; cerebellum; mouse; transcription factor; EXTRAMURAL MIGRATORY STREAM; PRECEREBELLAR NEURONS; RHOMBIC LIP; PONTOCEREBELLAR SYSTEM; PONTINE PROJECTIONS; GENE-TRANSFER; MOUSE ZIC1; CEREBELLAR; EXPRESSION; NUCLEI;
D O I
10.1016/j.neuroscience.2009.02.082
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Pontine gray neurons of the brain stem are a major source of mossy fiber (MF) afferents to granule cells of the cerebellum. Achieving this connectivity involves an early regionalization of pontine gray neuron cell bodies within the brainstem pontine nuclei, as well as establishing the proper ratio of crossed versus uncrossed MF projections to contralateral versus ipsilateral cerebellar territories. Here, we report expression of the transcription factor Zic1 in newly postmitotic pontine gray neurons and present functional experiments in embryonic and postnatal mice that implicate Zic1 levels as a key determinant of pontine neuron cell body position within the pons and axon laterality. Reducing Zic1 levels embryonically via in utero electroporation of short hairpin RNA interference (shRNAi) vectors shifted the postnatal distribution of pontine neurons from caudolateral to rostromedial territories; by contrast, increasing Zic1 levels resulted in the reciprocal shift, with electroporated cells redistributing caudolaterally. Associated with the latter was a change in axon laterality, with a greater proportion of marked projections now targeting the ipsilateral instead of contralateral cerebellum. Zic1 levels in pontine gray neurons, therefore, play an important role in the development of pontocerebellar circuitry. (C) 2009 IBRO. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:560 / 573
页数:14
相关论文
共 65 条
[21]   Assembly of the brainstem cochlear nuclear complex is revealed by intersectional and subtractive genetic fate maps [J].
Farago, AF ;
Awatramani, RB ;
Dymecki, SM .
NEURON, 2006, 50 (02) :205-218
[22]   Phenotype of mice lacking functional Deleted in colorectal cancer (Dcc) gene [J].
Fazeli, A ;
Dickinson, SL ;
Hermiston, ML ;
Tighe, RV ;
Steen, RG ;
Small, CG ;
Stoeckli, ET ;
KeinoMasu, K ;
Masu, M ;
Rayburn, H ;
Simons, J ;
Bronson, RT ;
Gordon, JI ;
TessierLavigne, M ;
Weinberg, RA .
NATURE, 1997, 386 (6627) :796-804
[23]   The E-protein Tcf4 interacts with Math1 to regulate differentiation of a specific subset of neuronal progenitors [J].
Flora, Adriano ;
Garcia, Jesus J. ;
Thaller, Christina ;
Zoghbi, Huda Y. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2007, 104 (39) :15382-15387
[24]   Zic2 promotes axonal divergence at the optic chiasm midline by EphB1-dependent and -independent mechanisms [J].
Garcia-Frigola, Cristina ;
Carreres, Maria Isabel ;
Vegar, Celia ;
Mason, Carol ;
Herrera, Eloisa .
DEVELOPMENT, 2008, 135 (10) :1833-1841
[25]   Hox paralog group 2 genes control the migration of mouse pontine neurons through Slit-Robo signaling [J].
Geisen, Marc J. ;
Di Meglio, Thomas ;
Pasqualetti, Massimo ;
Ducret, Sebastien ;
Brunet, Jean-Francois ;
Chedotal, Alain ;
Rijli, Filippo M. .
PLOS BIOLOGY, 2008, 6 (06) :1178-1194
[26]   Heterozygous deletion of the linked genes ZIC1 and ZIC4 is involved in Dandy-Walker malformation [J].
Grinberg, I ;
Northrup, H ;
Ardinger, H ;
Prasad, C ;
Dobyns, WB ;
Millen, KJ .
NATURE GENETICS, 2004, 36 (10) :1053-1055
[27]   Zic2 patterns binocular vision by specifying the uncrossed retinal projection [J].
Herrera, E ;
Brown, L ;
Aruga, J ;
Rachel, RA ;
Dolen, G ;
Mikoshiba, K ;
Brown, S ;
Mason, CA .
CELL, 2003, 114 (05) :545-557
[28]   THE MODIFIABLE NEURONAL NETWORK OF THE CEREBELLUM [J].
ITO, M .
JAPANESE JOURNAL OF PHYSIOLOGY, 1984, 34 (05) :781-792
[29]   Direct visualization of nucleogenesis by precerebellar neurons: involvement of ventricle-directed, radial fibre-associated migration [J].
Kawauchi, D ;
Taniguchi, H ;
Watanabe, H ;
Saito, T ;
Murakami, F .
DEVELOPMENT, 2006, 133 (06) :1113-1123
[30]   Deleted in Colorectal Cancer (DCC) encodes a netrin receptor [J].
KeinoMasu, K ;
Masu, M ;
Hinck, L ;
Leonardo, ED ;
Chan, SSY ;
Culotti, JG ;
TessierLavigne, M .
CELL, 1996, 87 (02) :175-185