| First Author | Yang T | Year | 2014 |
| Journal | Mol Genet Genomic Med | Volume | 2 |
| Issue | 2 | Pages | 138-51 |
| PubMed ID | 24689077 | Mgi Jnum | J:223183 |
| Mgi Id | MGI:5648171 | Doi | 10.1002/mgg3.53 |
| Citation | Yang T, et al. (2014) Analysis of PRICKLE1 in human cleft palate and mouse development demonstrates rare and common variants involved in human malformations. Mol Genet Genomic Med 2(2):138-51 |
| abstractText | Palate development is shaped by multiple molecular signaling pathways, including the Wnt pathway. In mice and humans, mutations in both the canonical and noncanonical arms of the Wnt pathway manifest as cleft palate, one of the most common human birth defects. Like the palate, numerous studies also link different Wnt signaling perturbations to varying degrees of limb malformation; for example, shortened limbs form in mutations of Ror2,Vangl2 (looptail) and, in particular, Wnt5a. We recently showed the noncanonical Wnt/planar cell polarity (PCP) signaling molecule Prickle1 (Prickle ilike 1) also stunts limb growth in mice. We now expanded these studies to the palate and show that Prickle1 is also required for palate development, ilike Wnt5a and Ror2. Unlike in the limb, the Vangl2looptail mutation only aggravates palate defects caused by other mutations. We screened Filipino cleft palate patients and found PRICKLE1 variants, both common and rare, at an elevated frequency. Our results reveal that in mice and humans PRICKLE1 directs palate morphogenesis; our results also uncouple Prickle1 function from Vangl2 function. Together, these findings suggest mouse and human palate development is guided by PCP-Prickle1 signaling that is probably not downstream of Vangl2. |
