Different levels of repressor activity assign redundant and specific roles to Nkx6 genes in motor neuron and interneuron specification

被引:212
作者
Vallstedt, A
Muhr, J
Pattyn, A
Pierani, A
Mendelsohn, M
Sander, M
Jessell, TM
Ericson, J [1 ]
机构
[1] Karolinska Inst, Med Nobel Inst, Dept Cell & Mol Biol, S-17177 Stockholm, Sweden
[2] Columbia Univ, Howard Hughes Med Inst, Dept Biochem & Mol Biophys, New York, NY 10032 USA
[3] Univ Hamburg, Ctr Mol Neurobiol, D-20251 Hamburg, Germany
关键词
D O I
10.1016/S0896-6273(01)00412-3
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Specification of neuronal fate in the vertebrate central nervous system depends on the profile of transcription factor expression by neural progenitor cells, but the precise roles of such factors in neurogenesis remain poorly characterized. Two closely related transcriptional repressors, Nkx6.2 and Nkx6.1, are expressed by progenitors in overlapping domains of the ventral spinal cord. We provide genetic evidence that differences in the level of repressor activity of these homeodomain proteins underlies the diversification of interneuron subtypes, and provides a fail-safe mechanism during motor neuron generation. A reduction in Nkx6 activity further permits VO neurons to be generated from progenitors that lack homeodomain proteins normally required for their generation, providing direct evidence for a model in which progenitor homeodomain proteins direct specific cell fates by actively suppressing the expression of transcription factors that direct alternative fates.
引用
收藏
页码:743 / 755
页数:13
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