| Literature DB >> 27452460 |
Qiangqiang Zhang1, Yue Zhang1, Chunyang Wang1, Zhejun Xu1, Qifei Liang1, Lei An1, Jiwen Li1, Zhidong Liu1, Yan You1, Miao He1, Ying Mao2, Bin Chen3, Zhi-Qi Xiong4, John L Rubenstein5, Zhengang Yang6.
Abstract
Striatal medium-sized spiny neurons (MSNs), composed of striatonigral and striatopallidal neurons, are derived from the lateral ganglionic eminence (LGE). We find that the transcription factor Sp9 is expressed in LGE progenitors that generate nearly all striatal MSNs and that Sp9 expression is maintained in postmitotic striatopallidal MSNs. Sp9-null mice lose most striatopallidal MSNs because of decreased proliferation of striatopallidal MSN progenitors and increased Bax-dependent apoptosis, whereas the development of striatonigral neurons is largely unaffected. ChIP qPCR provides evidence that Ascl1 directly binds the Sp9 promoter. RNA-seq and in situ hybridization reveal that Sp9 promotes expression of Adora2a, P2ry1, Gpr6, and Grik3 in the LGE and striatum. Thus, Sp9 is crucial for the generation, differentiation, and survival of striatopallidal MSNs.Entities:
Keywords: Adora2a; Ascl1; Drd2; LGE; Sp9; striatopallidal neuron; striatum
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Year: 2016 PMID: 27452460 PMCID: PMC4972643 DOI: 10.1016/j.celrep.2016.06.090
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423