Threshold-specific requirements for Bmp4 in mandibular development

被引:120
|
作者
Liu, W
Selever, J
Murali, D
Sun, XX
Brugger, SM
Ma, LJ
Schwartz, RJ
Maxson, R
Furuta, Y
Martin, JF
机构
[1] Texas A&M Syst Hlth Sci Ctr, Allek Inst Biosci & Technol, Houston, TX 77030 USA
[2] Univ Texas, Grad Sch Biomed Sci, Program Genes & Dev, Houston, TX 77030 USA
[3] Univ Texas, MD Anderson Canc Ctr, Dept Biochem & Mol Biol, Houston, TX 77030 USA
[4] Univ So Calif, Keck Sch Med, Norris Canc Hosp, Dept Biochem & Mol Biol, Los Angeles, CA 90033 USA
关键词
bone morphogenetic protein; craniofacial morphogenesis;
D O I
10.1016/j.ydbio.2005.04.019
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Mandibular development is regulated by an interplay between a specified branchial arch ectoderm and a plastic mesenchyme. Moreover, signaling from the pharyngeal endoderm has been shown to be important for mandibular morphogenesis. To gain insight into the mechanisms regulating mandibular pattern, it is important to investigate the function of the epithelial-derived signals. Bmp4 is expressed in both distal, mandibular arch ectoderm and pharyngeal endoderm. Here, we show that deletion of Bmp4 in the mandibular ectoderm and to a lesser extent in the pharyngeal endoderm, resulted in severe defects in mandibular development. Furthermore, our data uncovered different Bmp4 thresholds for expression of the Bmp-dependent Msx1 and Msx2 genes in mandibular mesenchyme. We also found that ectodermal Fgf8 expression was both activated and repressed by Bmp4 in a dosage-dependent fashion indicating a novel Bmp4 function in threshold-specific regulation of Fe transcription. Lastly, we provide evidence that Prx homeobox genes repress expression of an Msx2 transgene, previously shown to be Bmp4-responsive, revealing a mechanism for differential regulation of Msx1 and Msx2 by Pmp signaling. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:282 / 293
页数:12
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