Hanashima Carina, Li Suzanne C, Shen Lijian, Lai Eseng, Fishell Gord
Developmental Genetics Program and the Department of Cell Biology, The Skirball Institute of Biomolecular Medicine, New York University Medical Center, 540 First Avenue, New York, NY 10016, USA.
Science. 2004 Jan 2;303(5654):56-9. doi: 10.1126/science.1090674.
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.
在哺乳动物大脑皮质发生过程中,祖细胞能够产生的神经元类型逐渐受到限制。决定早期和晚期出生神经元命运的分子机制尚不清楚。我们在此证明,最早出生的神经元——Cajal-Retzius细胞的产生受到端脑转录因子Foxg1的抑制。在Foxg1基因敲除突变体中,我们观察到皮质中Cajal-Retzius神经元的产生过多。通过有条件地使正常产生深层皮质神经元的皮质祖细胞中的Foxg1失活,我们证明Foxg1对于抑制Cajal-Retzius细胞命运是持续必需的。因此,在后期皮质发育过程中产生最早出生神经元的能力被主动抑制但并未丧失。