Foxg1 suppresses early cortical cell fate

被引:310
作者
Hanashima, C
Li, SC
Shen, LJ
Lai, ES
Fishell, G
机构
[1] NYU, Med Ctr, Dev Genet Program, New York, NY 10016 USA
[2] NYU, Med Ctr, Skirball Inst Biomol Med, Dept Cell Biol, New York, NY 10016 USA
[3] Mem Sloan Kettering Canc Ctr, Cell Biol Program, New York, NY 10021 USA
[4] Cornell Univ, Weill Med Coll, Dept Physiol & Biophys, New York, NY 10021 USA
关键词
D O I
10.1126/science.1090674
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 mammalian cerebral corticogenesis, progenitor cells become progressively restricted in the types of neurons they can produce. The molecular mechanism that determines earlier versus later born neuron fate is unknown. We demonstrate here that the generation of the earliest born neurons, the Cajal-Retzius cells, is suppressed by the telencephalic transcription factor Foxg1. In Foxg1 null mutants, we observed an excess of Cajal-Retzius neuron production in the cortex. By conditionally inactivating Foxg1 in cortical progenitors that normally produce deep-layer cortical neurons, we demonstrate that Foxg1 is constitutively required to suppress Cajal-Retzius cell fate. Hence, the competence to generate the earliest born neurons during later cortical development is actively suppressed but not lost.
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页码:56 / 59
页数:4
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