TBR1 directly represses Fezf2 to control the laminar origin and development of the corticospinal tract

被引:152
作者
Han, Wenqi [1 ]
Kwan, Kenneth Y. [1 ]
Shim, Sungbo [1 ]
Lam, Mandy M. S. [1 ]
Shin, Yurae [1 ]
Xu, Xuming [1 ]
Zhu, Ying [1 ]
Li, Mingfeng [1 ]
Sestan, Nenad [1 ]
机构
[1] Yale Univ, Sch Med, Dept Neurobiol, Kavli Inst Neurosci, New Haven, CT 06510 USA
基金
美国国家卫生研究院;
关键词
neocortex; pyramidal neuron; axon guidance; transcriptional repression; CEREBRAL-CORTEX; PROJECTION NEURONS; MOTOR CONTROL; DIFFERENTIATION; SPECIFICATION; EXPRESSION; PATHWAYS; SYSTEM; MOUSE;
D O I
10.1073/pnas.1016723108
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The corticospinal (CS) tract is involved in controlling discrete voluntary skilled movements in mammals. The CS tract arises exclusively from layer (L) 5 projection neurons of the cerebral cortex, and its formation requires L5 activity of Fezf2 (Fezl, Zfp312). How this L5-specific pattern of Fezf2 expression and CS axonal connectivity is established with such remarkable fidelity had remained elusive. Here we show that the transcription factor TBR1 directly binds the Fezf2 locus and represses its activity in L6 corticothalamic projection neurons to restrict the origin of the CS tract to L5. In Tbr1 null mutants, CS axons ectopically originate from L6 neurons in a Fezf2-dependent manner. Consistently, misexpression of Tbr1 in L5 CS neurons suppresses Fezf2 expression and effectively abolishes the CS tract. Taken together, our findings show that TBR1 is a direct transcriptional repressor of Fezf2 and a negative regulator of CS tract formation that restricts the laminar origin of CS axons specifically to L5.
引用
收藏
页码:3041 / 3046
页数:6
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