Hox repertoires for motor neuron diversity and connectivity gated by a single accessory factor, FoxP1

被引:280
作者
Dasen, Jeremy S. [1 ,3 ,4 ,5 ]
De Camilli, Alessandro [1 ]
Wang, Bin [2 ]
Tucker, Philip W. [2 ]
Jessell, Thomas M. [3 ,4 ,5 ]
机构
[1] NYU, Sch Med, Dept Physiol & Neurosci, Smilow Neurosci Program, New York, NY 10016 USA
[2] Univ Texas Austin, Dept Mol Genet & Microbiol, Austin, TX 78712 USA
[3] Columbia Univ, Kavli Inst Brain Sci, Howard Hughes Med Inst, Dept Neurosci, New York, NY 10032 USA
[4] Columbia Univ, Kavli Inst Brain Sci, Howard Hughes Med Inst, Dept Biochem, New York, NY 10032 USA
[5] Columbia Univ, Kavli Inst Brain Sci, Howard Hughes Med Inst, Dept Mol Biophys, New York, NY 10032 USA
基金
英国惠康基金;
关键词
D O I
10.1016/j.cell.2008.06.019
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The precision with which motor neurons innervate target muscles depends on a regulatory network of Hox transcription factors that translates neuronal identity into patterns of connectivity. We show that a single transcription factor, FoxP1, coordinates motor neuron subtype identity and connectivity through its activity as a Hox accessory factor. FoxP1 is expressed in Hox-sensitive motor columns and acts as a dose-dependent determinant of columnar fate. Inactivation of Foxp1 abolishes the output of the motor neuron Hox network, reverting the spinal motor system to an ancestral state. The loss of FoxP1 also changes the pattern of motor neuron connectivity, and in the limb motor axons appear to select their trajectories and muscle targets at random. Our findings show that FoxP1 is a crucial determinant of motor neuron diversification and connectivity, and clarify how this Hox regulatory network controls the formation of a topographic neural map.
引用
收藏
页码:304 / 316
页数:13
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