A direct role for Sox10 in specification of neural crest-derived sensory neurons

被引:237
作者
Carney, Thomas J.
Dutton, Kirsten A.
Greenhill, Emma
Delfino-Machin, Mariana
Dufourcq, Pascale
Blader, Patrick
Kelsh, Robert N. [1 ]
机构
[1] Univ Bath, Ctr Regenerat Med, Dev Biol Programme, Dept Biol & Biochem, Bath BA2 7AY, Avon, England
[2] Univ Toulouse 3, UMR 5547, Ctr Dev Biol, F-31062 Toulouse, France
来源
DEVELOPMENT | 2006年 / 133卷 / 23期
基金
英国医学研究理事会; 英国生物技术与生命科学研究理事会; 英国惠康基金;
关键词
Sox10; neural crest; fate specification; determination; dorsal root ganglion; neurogenin; zebrafish; transgene; Waardenburg-Shah syndrome;
D O I
10.1242/dev.02668
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
sox10 is necessary for development of neural and pigment cell derivatives of the neural crest ( NC). However, whereas a direct role for Sox10 activity has been established in pigment and glial lineages, this is more controversial in NC-derived sensory neurons of the dorsal root ganglia (DRGs). We proposed that sox10 functioned in specification of sensory neurons, whereas others suggested that sensory neuronal defects were merely secondary to absence of glia. Here we provide evidence that in zebrafish, early DRG sensory neuron survival is independent of differentiated glia. Critically, we demonstrate that Sox10 is expressed transiently in the sensory neuron lineage, and species sensory neuron precursors by regulating the proneural gene neurogenin1. Consistent with this, we have isolated a novel sox10 mutant that lacks glia and yet displays a neurogenic DRG phenotype. In conjunction with previous findings, these data establish the generality of our model of Sox10 function in NC fate specification.
引用
收藏
页码:4619 / 4630
页数:12
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