Id sustains Hes1 expression to inhibit precocious neurogenesis by releasing negative autoregulation of Hes1

被引:178
作者
Bai, Ge
Sheng, Nengyin
Xie, Zhihui
Bian, Wei
Yokota, Yoshifumi
Benezra, Robert
Kageyama, Ryoichiro
Guillemot, Francois
Jing, Naihe
机构
[1] Chinese Acad Sci, Shanghai Inst Biol Sci, Inst Biochem & Cell Biol, Mol Cell Biol Lab Key Lab Stem Cell Biol, Shanghai 200031, Peoples R China
[2] Univ Fukui, Sch Med, Dept Mol Genet, Matsuoka, Fukui 9101193, Japan
[3] Mem Sloan Kettering Canc Ctr, Dept Canc Biol & Genet, New York, NY 10021 USA
[4] Kyoto Univ, Inst Virus Res, Kyoto 606, Japan
[5] Natl Inst Med Res, Div Mol Neurobiol, London NW7 1AA, England
基金
英国医学研究理事会;
关键词
D O I
10.1016/j.devcel.2007.05.014
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Negative bHLH transcription factor Hes1 can inhibit neural stem cells (NSCs) from precocious neurogenesis through repressing proneural gene expression; therefore, sustenance of Hes1 expression is crucial for NSC pool maintenance. Here we find that Ids, the dominant-negative regulators of proneural proteins, are expressed prior to proneural genes and share an overlapping expression pattern with Hes1 in the early neural tube of chick embryos. Overexpression of Id2 in the chick hindbrain upregulates Hes1 expression and inhibits proneural gene expression and neuronal differentiation. By contrast, Hes1 expression decreases, proneural gene expression expands, and neurogenesis occurs precociously in Id1;Id3 double knockout mice and in Id1-3 RNAi-electroporated chick embryos. Mechanistic studies show that Id proteins interact directly with Hes1 and release the negative feedback autoregulation of Hes1 without interfering with its ability to affect other target genes. These results indicate that Id proteins participate in NSC maintenance through sustaining Hes1 expression in early embryos.
引用
收藏
页码:283 / 297
页数:15
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