Possible Effect of Snail Family Transcriptional Repressor 1 Polymorphisms in Non-Syndromic Cleft Lip With or Without Cleft Palate Publisher Pubmed



Cura F¹ ; Palmieri A¹ ; Girardi A¹ ; Carinci F² ; Morselli PG^{1, 3} ; Nouri N⁴ ; Pezzetti F¹ ; Scapoli L¹ ; Martinelli M¹
Source: Clinical Oral Investigations Published:2018

Abstract

Objective: Orofacial development is a complex process subjected to failure impairing. Indeed, the cleft of the lip and/or of the palate is among the most frequent inborn malformations. The JARID2 gene has been suggested to be involved in non-syndromic cleft lip with or without cleft palate (nsCL/P) etiology. JARID2 interacts with the polycomb repressive complex 2 (PRC2) in regulating the expression patterns of developmental genes by modifying the chromatin state. Materials and methods: Genes coding for the PRC2 components, as well as other genes active in cell differentiation and embryonic development, were selected for a family-based association study to verify their involvement in nsCL/P. A total of 632 families from Italy and Asia participated to the study. Results: Evidence of allelic association was found with polymorphisms of SNAI1; in particular, the rs16995010-G allele was undertransmitted to the nsCL/P cases [P = 0.004, odds ratio = 0.69 (95% C.I. 0.54–0.89)]. However, the adjusted significance value corrected for all the performed tests was P = 0.051. Conclusions: The findings emerging by the present study suggest for the first time an involvement of SNAI1 in the nsCL/P onset. Clinical relevance: Interestingly, SNAI1 is known to promote epithelial to mesenchymal transition by repressing E-cadherin expression, but it needs an intact PRC2 to act this function. Alterations of this process could contribute to the complex etiology of nsCL/P. © 2018, Springer-Verlag GmbH Germany, part of Springer Nature.