SP8 and SP9 coordinately promote D2-type medium spiny neuron production by activating Six3 expression

SP8 和 SP9 通过激活 Six3 表达协同促进 D2 型中型棘状神经元的产生。

阅读:2
作者:Zhejun Xu ,Qifei Liang ,Xiaolei Song ,Zhuangzhi Zhang ,Susan Lindtner ,Zhenmeiyu Li ,Yan Wen ,Guoping Liu ,Teng Guo ,Dashi Qi ,Min Wang ,Chunyang Wang ,Hao Li ,Yan You ,Xin Wang ,Bin Chen ,Hua Feng ,John L Rubenstein ,Zhengang Yang

Abstract

Dopamine receptor DRD1-expressing medium spiny neurons (D1 MSNs) and dopamine receptor DRD2-expressing medium spiny neurons (D2 MSNs) are the principal projection neurons in the striatum, which is divided into dorsal striatum (caudate nucleus and putamen) and ventral striatum (nucleus accumbens and olfactory tubercle). Progenitors of these neurons arise in the lateral ganglionic eminence (LGE). Using conditional deletion, we show that mice lacking the transcription factor genes Sp8 and Sp9 lose virtually all D2 MSNs as a result of reduced neurogenesis in the LGE, whereas D1 MSNs are largely unaffected. SP8 and SP9 together drive expression of the transcription factor Six3 in a spatially restricted domain of the LGE subventricular zone. Conditional deletion of Six3 also prevents the formation of most D2 MSNs, phenocopying the Sp8/9 mutants. Finally, ChIP-Seq reveals that SP9 directly binds to the promoter and a putative enhancer of Six3 Thus, this study defines components of a transcription pathway in a regionally restricted LGE progenitor domain that selectively drives the generation of D2 MSNs. Keywords: DRD2; LGE; Medium spiny neuron; Mouse; Six3; Sp8; Sp9; Striatum.

特别声明

1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。

2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。

3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。

4、投稿及合作请联系:info@biocloudy.com。