Fezl regulates the differentiation and axon targeting of layer 5 subcortical projection neurons in cerebral cortex

被引:258
作者
Chen, B [1 ]
Schaevitz, LR [1 ]
McConnell, SK [1 ]
机构
[1] Stanford Univ, Dept Biol Sci, Stanford, CA 94305 USA
关键词
axon guidance; cell fate; corticospinal tract; zinc-finger transcription factor;
D O I
10.1073/pnas.0508732102
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
During the development of the cerebral cortex, progenitor cells produce neurons that migrate to laminar positions appropriate for their birth dates, adopt specific neuronal identities, and form appropriate local and long-distance axonal connections. Here, we report that forebrain embryonic zinc-finger-like protein (Fezl), a putative zinc-finger transcriptional repressor, is required for the differentiation of projection neurons in cortical layer 5. In Fezl-deficient mice, these neurons display molecular, morphological, and axonal targeting defects. The corticospinal tract was absent in Fezl(-/-) mice, corticotectal and pontine projections were severely reduced, and Fezl-expressing neurons formed aberrant axonal projections. The expression of many molecular markers for deep-layer neurons was reduced or absent in the Fezl(-/-) cerebral cortex. Most strikingly, Ctip2, a transcription factor required for the formation of the corticospinal tract, was not expressed in the Fezl-deficient cortex. These results suggest that Fezl regulates the differentiation of layer 5 subcortical projection neurons.
引用
收藏
页码:17184 / 17189
页数:6
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