Zinc finger genes Fezf1 and Fezf2 control neuronal differentiation by repressing Hes5 expression in the forebrain

被引:66
作者
Shimizu, Takeshi [1 ]
Nakazawa, Masato [1 ]
Kani, Shuichi [1 ]
Bae, Young-Ki [1 ]
Shimizu, Takashi [1 ,3 ]
Kageyama, Ryoichiro [2 ]
Hibi, Masahiko [1 ,3 ]
机构
[1] RIKEN, Ctr Dev Biol, Lab Vertebrate Axis Format, Kobe, Hyogo 6500047, Japan
[2] Kyoto Univ, Inst Virus Res, Kyoto 6068507, Japan
[3] Nagoya Univ, Biosci & Biotechnol Ctr, Nagoya, Aichi 4648601, Japan
来源
DEVELOPMENT | 2010年 / 137卷 / 11期
关键词
Corticogenesis; Neurogenesis; Zinc finger genes; Fezf1; Fezf2; Hes5; neurogenin; 2; Mouse; CAJAL-RETZIUS CELLS; DEVELOPING CEREBRAL-CORTEX; ADULT ZEBRAFISH BRAIN; NEURAL STEM-CELLS; SUBCORTICAL PROJECTION NEURONS; SUBPLATE NEURONS; PROGENITOR CELLS; THALAMOCORTICAL AXONS; EXTRACELLULAR-MATRIX; RADIAL GLIA;
D O I
10.1242/dev.047167
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Precise control of neuronal differentiation is necessary for generation of a variety of neurons in the forebrain. However, little is known about transcriptional cascades, which initiate forebrain neurogenesis. Here we show that zinc finger genes Fezf1 and Fezf2, which encode transcriptional repressors, are expressed in the early neural stem (progenitor) cells and control neurogenesis in mouse dorsal telencephalon. Fezf1-and Fezf2-deficient forebrains display upregulation of Hes5 and downregulation of neurogenin 2, which is known to be negatively regulated by Hes5. We show that FEZF1 and FEZF2 bind to and directly repress the promoter activity of Hes5. In Fezf1-and Fezf2-deficient telencephalon, the differentiation of neural stem cells into early-born cortical neurons and intermediate progenitors is impaired. Loss of Hes5 suppresses neurogenesis defects in Fezf1-and Fezf2-deficient telencephalon. Our findings reveal that Fezf1 and Fezf2 control differentiation of neural stem cells by repressing Hes5 and, in turn, by derepressing neurogenin 2 in the forebrain.
引用
收藏
页码:1875 / 1885
页数:11
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