The canonical Wnt pathway directly regulates NRSF/REST expression in chick spinal cord

被引:65
作者
Nishihara, S
Tsuda, L
Ogura, T
机构
[1] Tohoku Univ, Inst Dev Aging & Canc, Sendai, Miyagi 9808575, Japan
[2] RIKEN, Ctr Dev Biol, Lab Morphogenet Signaling, Chou Ku, Kobe, Hyogo 6500047, Japan
关键词
Wnt1; NRSF/REST; beta-catenin; canonical wnt pathway; spinal cord; progenitor cells; in ovo electroporation;
D O I
10.1016/j.bbrc.2003.09.158
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Neural precursor cells actively proliferate in the ventricular zone to self-renew the stem cell population, and in parallel, maintain their undifferentiated state. This progenitor pool generates postmitotic cells that migrate to the mantle layer and differentiate into mature neurons. The growth of these stem cells is strictly controlled by the canonical Wnt signaling cascade, in part mediated by the direct regulation of Cyclin D1, a critical regulator of cell cycle progression. Here, we report that the canonical Wnt pathway directly controls the expression of NRSF/REST. The Wnt-activated beta-catenin/TCF complex up-regulates this gene through a conserved element found in its exon 1a, a critical result obtained by a novel in ovo transcriptional assay. Hence, our data show that the canonical Wnt signaling cascade directly regulates the NRSF/REST and Cyclin D1 genes, thereby controlling the progenitor cells. In addition, we show that our in ovo transcription assay is a powerful way to analyze gene regulation in a natural in vivo context. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:55 / 63
页数:9
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