SOX5 postmitotically regulates migration, postmigratory differentiation, and projections of subplate and deep-layer neocortical neurons

被引:210
作者
Kwan, Kenneth Y. [1 ,2 ]
Lam, Mandy M. S. [1 ,2 ]
Krsnik, Zeljka [1 ,2 ]
Kawasawa, Yuka Imamura [1 ,2 ]
Lefebvre, Veronique [3 ]
Sestan, Nenad [1 ,2 ]
机构
[1] Yale Univ, Dept Neurobiol, Sch Med, New Haven, CT 06520 USA
[2] Yale Univ, Kavli Inst Neurosci, Sch Med, New Haven, CT 06520 USA
[3] Cleveland Clin, Lerner Res Inst, Dept Cell Biol & Orthopaed Res Ctr, Cleveland, OH 44195 USA
基金
美国国家卫生研究院; 加拿大健康研究院;
关键词
neocortex development; postmitotic mechanisms; pyramidal neurons; Sox genes; transcriptional enhancer;
D O I
10.1073/pnas.0806791105
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
Neocortical projection neurons exhibit layer-specific molecular profiles and axonal connections. Here we Show that the molecular identities of early-born subplate and deep-layer neurons are not acquired solely during generation or shortly thereafter but undergo progressive postmitotic refinement mediated by SOX5. Fezf2 and Bcl11b, transiently expressed in all subtypes of newly postmigratory early-born neurons, are subsequently downregulated in layer 6 and subplate neurons, thereby establishing their layer 5-enriched postnatal patterns. In Sox5-null mice, this downregulation is disrupted, and layer 6 and subplate neurons maintain an immature differentiation state, abnormally expressing these genes postnatally. Consistent with this disruption, SOX5 binds and represses a conserved enhancer near Fezf2. The Sox5-null neocortex exhibits failed preplate partition and laminar inversion of early-born neurons, loss of layer 5 subcerebral axons, and misrourting of subplate and layer 6 corticothalamic axons to the hypothalamus. Thus, SOX5 postmitotically regulates the migration, postmigratory differentiation, and subcortical projections of subplate and deep-layer neurons.
引用
收藏
页码:16021 / 16026
页数:6
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