Transcriptional Networks Controlled by NKX2-1 in the Development of Forebrain GABAergic Neurons

被引:86
|
作者
Sandberg, Magnus [1 ]
Flandin, Pierre [1 ,7 ]
Silberberg, Shanni [1 ]
Su-Feher, Linda [2 ,3 ]
Price, James D. [1 ]
Hu, Jia Sheng [1 ]
Kim, Carol [1 ]
Visel, Axel [4 ,5 ,6 ]
Nord, Alex S. [2 ,3 ]
Rubenstein, John L. R. [1 ]
机构
[1] Univ Calif San Francisco, Dept Psychiat, San Francisco, CA 94143 USA
[2] Univ Calif Davis, Dept Psychiat & Behav Sci, Sacramento, CA 95817 USA
[3] Univ Calif Davis, Dept Neurobiol Physiol & Behav, Davis, CA 95616 USA
[4] Lawrence Berkeley Natl Lab, Berkeley, CA 94720 USA
[5] US DOE, Joint Genome Inst, Walnut Creek, CA 94598 USA
[6] Univ Calif, Sch Nat Sci, Merced, CA 95343 USA
[7] Quanticel Pharmaceut, San Francisco, CA 94158 USA
关键词
EMBRYONIC STEM-CELLS; CORTICAL INTERNEURON FATE; VENTRAL NEURAL-TUBE; HOMEOBOX GENE LHX8; EPIGENETIC SIGNATURE; REGULATORY ELEMENTS; LUNG ADENOCARCINOMA; SPECIFICATION; TELENCEPHALON; EXPRESSION;
D O I
10.1016/j.neuron.2016.08.020
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The embryonic basal ganglia generates multiple projection neurons and interneuron subtypes from distinct progenitor domains. Combinatorial interactions of transcription factors and chromatin are thought to regulate gene expression. In the medial ganglionic eminence, the NKX2-1 transcription factor controls regional identity and, with LHX6, is necessary to specify pallidal projection neurons and fore-brain interneurons. Here, we dissected the molecular functions of NKX2-1 by defining its chromosomal binding, regulation of gene expression, and epigenetic state. NKX2-1 binding at distal regulatory elements led to a repressed epigenetic state and transcriptional repression in the ventricular zone. Conversely, NKX2-1 is required to establish a permissive chromatin state and transcriptional activation in the sub-ventricular and mantle zones. Moreover, combinatorial binding of NKX2-1 and LHX6 promotes transcriptionally permissive chromatin and activates genes expressed in cortical migrating interneurons. Our integrated approach provides a foundation for elucidating transcriptional networks guiding the development of the MGE and its descendants.
引用
收藏
页码:1260 / 1275
页数:16
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