, Volume 351, Issue 3, pp 445-452
Date: 13 Nov 2012

Gene expression changes in the secondary palate and mandible of Prdm16 −/− mice

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Abstract

Loss of Prdm16 expression in the mouse leads to a complete cleft of the secondary palate. We have now determined changes in gene expression in the secondary palates of Prdm16 −/− fetuses in an attempt to reveal the mechanism(s) leading to the failure of palate closure in these mice. Defined pathway-based polymerase chain reaction arrays were used to analyze the expression of genes associated with the extracellular matrix and the transforming growth factor-β and bone morphogenetic protein signaling networks, perturbations of which can lead to palatal clefting. Loss of Prdm16 expression in the secondary palate leads to alterations in numerous genes within these groups, many of which have been linked to chondrogenesis and osteogenesis. The expression of several genes linked to bone development was significantly changed in the developing secondary palate. Analysis of gene expression in the mandibles of Prdm16 −/− fetuses revealed similar alterations in the same gene set. These data suggest that one function of Prdm16 is the regulation of genes that play a role in the differentiation of mesenchymal cells into chondro-/osteocytes.

This work was supported in part by NIH grants DE018215, HD053509 and P20 RR017702 from the COBRE program of the National Center for Research Resources and the NIGMS. Additional support was provided by the Kentucky Science and Engineering Foundation.
The authors declare no conflicts of interest, commercial or financial.