Targeted disruption of mammalian hairy and Enhancer of split homolog-1 (HES-1) leads to up-regulation of neural helix-loop-helix factors, premature neurogenesis, and severe neural tube defects

被引:593
作者
Ishibashi, M
Ang, SL
Shiota, K
Nakanishi, S
Kageyama, R
Guillemot, F
机构
[1] KYOTO UNIV,INST IMMUNOL,KYOTO,JAPAN
[2] KYOTO UNIV,FAC MED,DEPT ANAT,KYOTO,JAPAN
[3] RES DEV CORP JAPAN,PRESTO,KYOTO,JAPAN
[4] UNIV STRASBOURG 1,COLL FRANCE,INSERM,CNRS,INST GENET & BIOL MOLEC & CELLULAIRE,STRASBOURG,FRANCE
关键词
gene targeting; neurogenesis; neural tube defect; HES genes; Mash-1;
D O I
10.1101/gad.9.24.3136
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Mammalian hairy and Enhancer of split homolog-1 (HES-1) encodes a helix-loop-helix (HLH) factor that is thought to act as a negative regulator of neurogenesis. To directly investigate the functions of HES-1 in mammalian embryogenesis, we performed a targeted disruption of the HES-1 locus. Mice homozygous for the mutation exhibited severe neurulation defects and died during gestation or just after birth. In the developing brain of HES-1-null embryos, expression of the neural differentiation factor Mash-1 and other neural HLH Factors was up-regulated and postmitotic neurons appeared prematurely. These results suggest that HES-I normally controls the proper timing of neurogenesis and regulates neural tube morphogenesis.
引用
收藏
页码:3136 / 3148
页数:13
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