Brn-1 and Brn-2 share crucial roles in the production and positioning of mouse neocortical neurons

被引:194
作者
Sugitani, Y
Nakai, S
Minowa, O
Nishi, M
Jishage, K
Kawano, H
Mori, K
Ogawa, M
Noda, T [1 ]
机构
[1] JFCR Canc Inst, Dept Cell Biol, Tokyo 1708455, Japan
[2] RIKEN, Genom Sci Ctr, Mouse Funct Genom Res Grp, Kanagawa 2440804, Japan
[3] Tokyo Metropolitan Inst Neurosci, Dept Dev Morphol, Tokyo 1838526, Japan
[4] Univ Tokyo, Grad Sch Med, Dept Physiol, Tokyo 1130033, Japan
[5] RIKEN, Brain Sci Inst, Lab Cell Culture Dev, Wako, Saitama 3510198, Japan
[6] Tohoku Univ, Sch Med, Dept Mol Genet, Sendai, Miyagi 9808575, Japan
[7] Japan Sci & Technol Corp, Core Res Evolut Sci & Technol, Saitama 3320012, Japan
关键词
POU; Brn-1; Brn-2; mDab1; neocortex;
D O I
10.1101/gad.978002
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Formation of highly organized neocortical structure depends on the production and correct placement of the appropriate number and types of neurons. POU homeodomain proteins Brn-1 and Brn-2 are coexpressed in the developing neocortex, both in the late precursor cells and in the migrating neurons. Here we show that double disruption of both Brn-1 and Brn-2 genes in mice leads to abnormal formation of the neocortex with dramatically reduced production of layer IV-II neurons and defective migration of neurons unable to express mDab1. These data indicate that Brn-1 and Brn-2 share roles in the production and positioning of neocortical neuron development.
引用
收藏
页码:1760 / 1765
页数:6
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