Multiple pathways governing Cdx1 expression during murine development

被引:84
|
作者
Prinos, P
Joseph, S
Oh, K
Meyer, BI
Gruss, P
Lohnes, D
机构
[1] Inst Rech Clin Montreal, Montreal, PQ H2W 1R7, Canada
[2] Max Planck Inst Biophys Chem, Dept Mol Cell Biol, D-37077 Gottingen, Germany
[3] Univ Montreal, Dept Mol Biol, Montreal, PQ H3T 1B9, Canada
[4] McGill Univ, Div Expt Med, Montreal, PQ H3A 2T5, Canada
基金
加拿大健康研究院;
关键词
retinoic acid receptor; Cdx; vertebral specification; Hox; Wnt3a; caudal;
D O I
10.1006/dbio.2001.0446
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Cdx1 encodes a mammalian homeobox gene involved in vertebral patterning. Retinoic acid (RA) is likewise implicated in vertebral patterning. We have previously shown that Cdx1 is a direct retinoid target gene, suggesting that Cdx1 may convey some of the effects of retinoid signaling. However, RA appears to be essential for only early stages of Cdx1 expression, and therefore other factors must be involved in maintaining later stages of expression. Based on function and pattern of expression, Wnt family members, in particular Wnt3a, are candidates for regulation of expression of Cdx1. Consistent with this, we confirm prior results which demonstrated that Cdx1 can be directly regulated by Wnt signaling, and identify functional LEF/TCF response motifs essential for this response. We also find that Cdx1 expression is markedly attenuated in a stage- and tissue-specific fashion in the Wnt3a hypomorph vestigial tail, and present data demonstrating that Wnt3a and RA synergize strongly to activate Cdx1. Finally, we show that Cdx1 positively regulates its own expression. These data prompt a model whereby retinoid and Wnt signaling function directly and synergistically to initiate Cdx1 expression in the caudal embryo. Expression is then maintained, at least in part, by an autoregulatory mechanism at later stages. (C) 2001 Academic Press.
引用
收藏
页码:257 / 269
页数:13
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