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Publication : Gene expression analysis reveals that formation of the mouse anterior secondary palate involves recruitment of cells from the posterior side.

First Author  Li Q Year  2007
Journal  Int J Dev Biol Volume  51
Issue  2 Pages  167-72
PubMed ID  17294368 Mgi Jnum  J:118668
Mgi Id  MGI:3700088 Doi  10.1387/ijdb.062212ql
Citation  Li Q, et al. (2007) Gene expression analysis reveals that formation of the mouse anterior secondary palate involves recruitment of cells from the posterior side. Int J Dev Biol 51(2):167-72
abstractText  Cleft palate is a common birth defect caused by disruptions in secondary palate development. Anterior-posterior (A-P) regional specification plays a critical role in palate development and fusion. Previous studies have shown that at the molecular level, the anterior palate can be defined by the expression of Shox-2 and the posterior palate by Meox-2 expression in certain mouse strains. Here, we have extended previous studies by performing a more detailed analysis of these genes during mouse palate development. We found that the expression patterns of Shox-2 and Meox-2 are dynamic during palate development. At embryonic day 12.5 (E12.5), Shox-2 expression is localized to the anterior end and its expression domain covers less than 25% of the length of the palate shelf. The Shox-2 expression domain then gradually expands towards the posterior end and ultimately occupies more than 60% of the palate shelf by E14.5. The expansion of the Shox-2 domain may involve induction of Shox2 expression in additional cells. Reciprocally, the Meox-2 expression domain at E12.5 covers a large portion of the palate shelf, a region more than 70% of the entire palate, but then regresses to the posterior 25% by E14.5. This regression is likely caused by the repression of Meox-2 expression in certain Meox2 expressing cells, rather than the cessation of cell proliferation. Therefore, certain Meox-2 positive 'primitive posterior cells' are differentiated/converted into Shox-2 positive 'definitive anterior cells' during A-P regional specification.
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