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对哺乳动物毛状和分裂增强子同源物-1(HES-1)进行靶向破坏会导致神经螺旋-环-螺旋因子上调、神经发生过早以及严重的神经管缺陷。

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.

作者信息

Ishibashi M, Ang S L, Shiota K, Nakanishi S, Kageyama R, Guillemot F

机构信息

Institute for Immunology, Kyoto University Faculty of Medicine, Japan.

出版信息

Genes Dev. 1995 Dec 15;9(24):3136-48. doi: 10.1101/gad.9.24.3136.

Abstract

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-1 normally controls the proper timing of neurogenesis and regulates neural tube morphogenesis.

摘要

哺乳动物的毛状和分裂增强子同源物1(HES-1)编码一种螺旋-环-螺旋(HLH)因子,该因子被认为是神经发生的负调节因子。为了直接研究HES-1在哺乳动物胚胎发育中的功能,我们对HES-1基因座进行了靶向破坏。该突变的纯合小鼠表现出严重的神经管形成缺陷,并在妊娠期或出生后不久死亡。在HES-1基因缺失胚胎的发育大脑中,神经分化因子Mash-1和其他神经HLH因子的表达上调,有丝分裂后神经元过早出现。这些结果表明,HES-1通常控制神经发生的正确时间,并调节神经管形态发生。

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