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Gene-gene interaction between MSX1 and TP63 in Asian case-parent trios with nonsyndromic cleft lip with or without cleft palate.
- Source :
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Birth defects research [Birth Defects Res] 2018 Mar 01; Vol. 110 (4), pp. 317-324. Date of Electronic Publication: 2018 Jan 17. - Publication Year :
- 2018
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Abstract
- Background: Small ubiquitin-like modification, also known as sumoylation, is a crucial post-translational regulatory mechanisms involved in development of the lip and palate. Recent studies reported two sumoylation target genes, MSX1 and TP63, to have achieved genome-wide level significance in tests of association with nonsyndromic clefts. Here, we performed a candidate gene analysis considering gene-gene and gene-environment interaction for SUMO1, MSX1, and TP63 to further explore the etiology of nonsyndromic cleft lip with or without cleft palate (NSCL/P).<br />Methods: A total of 130 single-nucleotide polymorphisms (SNPs) in or near SUMO1, MSX1, and TP63 was analyzed among 1,038 Asian NSCL/P trios ascertained through an international consortium. Conditional logistic regression models were used to explore gene-gene (G × G) and gene-environment (G × E) interaction involving maternal environmental tobacco smoke and multivitamin supplementation. Bonferroni correction was used for G × E analysis and permutation tests were used for G × G analysis.<br />Results: While transmission disequilibrium tests and gene-environment interaction analysis showed no significant results, we did find signals of gene-gene interaction between SNPs near MSX1 and TP63. Three pairwise interactions yielded significant p values in permutation tests (rs884690 and rs9290890 with p = 9.34 × 10 <superscript>-5</superscript> and empirical p = 1.00 × 10 <superscript>-4</superscript> , rs1022136 and rs4687098 with p = 2.41 × 10 <superscript>-4</superscript> and empirical p = 2.95 × 10 <superscript>-4</superscript> , rs6819546 and rs9681004 with p = 5.15 × 10 <superscript>-4</superscript> and empirical p = 3.02 × 10 <superscript>-4</superscript> ).<br />Conclusion: Gene-gene interaction between MSX1 and TP63 may influence the risk of NSCL/P in Asian populations. Our study provided additional understanding of the genetic etiology of NSCL/P and underlined the importance of considering gene-gene interaction in the etiology of this common craniofacial malformation.<br /> (© 2018 Wiley Periodicals, Inc.)
Details
- Language :
- English
- ISSN :
- 2472-1727
- Volume :
- 110
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- Birth defects research
- Publication Type :
- Academic Journal
- Accession number :
- 29341488
- Full Text :
- https://doi.org/10.1002/bdr2.1139