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      Molecular signaling along the anterior–posterior axis of early palate development

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          Abstract

          Cleft palate is a common congenital birth defect in humans. In mammals, the palatal tissue can be distinguished into anterior bony hard palate and posterior muscular soft palate that have specialized functions in occlusion, speech or swallowing. Regulation of palate development appears to be the result of distinct signaling and genetic networks in the anterior and posterior regions of the palate. Development and maintenance of expression of these region-specific genes is crucial for normal palate development. Numerous transcription factors and signaling pathways are now recognized as either anterior- (e.g., Msx1, Bmp4, Bmp2, Shh, Spry2, Fgf10, Fgf7, and Shox2) or posterior-specific (e.g., Meox2, Tbx22, and Barx1). Localized expression and function clearly highlight the importance of regional patterning and differentiation within the palate at the molecular level. Here, we review how these molecular pathways and networks regulate the anterior–posterior patterning and development of secondary palate. We hypothesize that the anterior palate acts as a signaling center in setting up development of the secondary palate.

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          Most cited references103

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          Abnormal lung development and cleft palate in mice lacking TGF-beta 3 indicates defects of epithelial-mesenchymal interaction.

          A broad spectrum of biological activities has been proposed for transforming growth factor-beta 3 (TGF-beta 3). To study TGF-beta 3 function in development, TGF-beta 3 null mutant mice were generated by gene-targeting. Within 20 hours of birth, homozygous TGF-beta 3-/- mice die with unique and consistent phenotypic features including delayed pulmonary development and defective palatogenesis. Unlike other null mutants with cleft palate, TGF-beta 3-/- mice lack other concomitant craniofacial abnormalities. This study demonstrates an essential function for TGF-beta 3 in the normal morphogenesis of palate and lung, and directly implicates this cytokine in mechanisms of epithelial-mesenchymal interaction.
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            Transforming growth factor-beta 3 is required for secondary palate fusion.

            Mice lacking TGF-beta 3 exhibit an incompletely penetrant failure of the palatal shelves to fuse leading to cleft palate. The defect appears to result from impaired adhesion of the apposing medial edge epithelia of the palatal shelves and subsequent elimination of the mid-line epithelial seam. No craniofacial abnormalities were observed. This result demonstrates that TGF-beta 3 affects palatal shelf fusion by an intrinsic, primary mechanism rather than by effects secondary to craniofacial defects.
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              A human MSX1 homeodomain missense mutation causes selective tooth agenesis.

              We demonstrate that a mutation in the homeobox gene, MSX1, causes a common developmental anomaly, familial tooth agenesis. Genetic linkage analyses in a family with autosomal dominant agenesis of second premolars and third molars identified a locus on chromosome 4p, where the MSX1 gene resides. Sequence analyses demonstrated an Arg31Pro missense mutation in the homeodomain of MSX1 in all affected family members. Arg 31 is a highly conserved homeodomain residue that interacts with the ribose phosphate backbone of target DNA. We propose that the Arg31 Pro mutatrion comprises MSX1 interactions, and suggest that MSX1 functions are critical for normal development of specific human teeth.
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                Author and article information

                Journal
                Front Physiol
                Front Physiol
                Front. Physio.
                Frontiers in Physiology
                Frontiers Media S.A.
                1664-042X
                07 January 2013
                2012
                : 3
                : 488
                Affiliations
                [1] 1Laboratory of Molecular Cell Biology, College of Pharmacy and Nutrition, University of Saskatchewan Saskatoon, SK, Canada
                [2] 2Department of Anatomy, Biochemistry and Physiology, University of Hawaii School of Medicine Honolulu, HI, USA
                Author notes

                Edited by: Daniel Graf, University of Zurich, Switzerland

                Reviewed by: Daniel Graf, University of Zurich, Switzerland; Claire A. Canning, A*STAR Agency for Science Technology and Research, Singapore; Carolina Parada, University of Southern California, USA

                *Correspondence: Adil J. Nazarali, Laboratory of Molecular Cell Biology, College of Pharmacy and Nutrition, University of Saskatchewan, 116 Thorvaldson Building, 110 Science Place, Saskatoon, SK S7N 5C9, Canada. e-mail: aj.nazarali@ 123456usask.ca

                This article was submitted to Frontiers in Craniofacial Biology, a specialty of Frontiers in Physiology.

                Article
                10.3389/fphys.2012.00488
                3539680
                23316168
                4649cc70-2f78-4a52-b620-4e7e1af17ec9
                Copyright © 2013 Smith, Lozanoff, Iyyanar and Nazarali.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc.

                History
                : 16 May 2012
                : 14 December 2012
                Page count
                Figures: 4, Tables: 0, Equations: 0, References: 125, Pages: 14, Words: 13805
                Categories
                Physiology
                Review Article

                Anatomy & Physiology
                anterior–posterior axis,development,growth factors,migration,secondary palate,signaling

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