4.8 Review

Msx homeobox gene family and craniofacial development

Journal

CELL RESEARCH
Volume 13, Issue 6, Pages 429-442

Publisher

SCIENCE CHINA PRESS
DOI: 10.1038/sj.cr.7290185

Keywords

Msx genes; craniofacial; tooth; cleft palate; suture; development; transcription factor; signaling molecule

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Funding

  1. NIDCR NIH HHS [R01DE14044, R01DE12329, P60DE13076] Funding Source: Medline

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Vertebrate Msx genes are unlinked, homeobox-containing genes that bear homology to the Drosophila muscle segment homeobox gene. These genes are expressed at multiple sites of tissue-tissue interactions during vertebrate embryonic development. Inductive interactions mediated by the Msx genes are essential for normal craniofacial, limb and ectodermal organ morphogenesis, and are also essential to survival in mice, as manifested by the phenotypic abnormalities shown in knockout mice and in humans. This review summarizes studies on the expression, regulation, and functional analysis of Msx genes that bear relevance to craniofacial development in humans and mice.

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