Literature DB >> 29341488

Gene-gene interaction between MSX1 and TP63 in Asian case-parent trios with nonsyndromic cleft lip with or without cleft palate.

Dongjing Liu1, Holger Schwender2, Mengying Wang1, Hong Wang1, Ping Wang3, Hongping Zhu4, Zhibo Zhou4, Jing Li4, Tao Wu1,5, Terri H Beaty6.   

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).
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.
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 × 10-5 and empirical p = 1.00 × 10-4 , rs1022136 and rs4687098 with p = 2.41 × 10-4 and empirical p = 2.95 × 10-4 , rs6819546 and rs9681004 with p = 5.15 × 10-4 and empirical p = 3.02 × 10-4 ).
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.
© 2018 Wiley Periodicals, Inc.

Entities:  

Keywords:  association study; case-parent trio; gene-gene interaction; nonsyndromic cleft lip with or without cleft palate; sumoylation

Mesh:

Substances:

Year:  2018        PMID: 29341488     DOI: 10.1002/bdr2.1139

Source DB:  PubMed          Journal:  Birth Defects Res            Impact factor:   2.344


  4 in total

1.  Gene-by-gene interactions associated with the risk of conotruncal heart defects.

Authors:  Chen Lyu; Daniel M Webber; Stewart L MacLeod; Charlotte A Hobbs; Ming Li
Journal:  Mol Genet Genomic Med       Date:  2019-12-18       Impact factor: 2.183

2.  PBX-WNT-P63-IRF6 pathway in nonsyndromic cleft lip and palate.

Authors:  Lorena Maili; Ariadne Letra; Renato Silva; Edward P Buchanan; John B Mulliken; Matthew R Greives; John F Teichgraeber; Steven J Blackwell; Rohit Ummer; Ryan Weber; Brett Chiquet; Susan H Blanton; Jacqueline T Hecht
Journal:  Birth Defects Res       Date:  2019-12-11       Impact factor: 2.344

3.  Association of single nucleotide polymorphisms at 20q12 with nonsyndromic cleft lip with or without cleft palate in a Southern Chinese Han cohort.

Authors:  Yunpu He; Liheng Huang; Yuqian Zheng; Jian-Huan Chen; Shijie Tang
Journal:  Mol Genet Genomic Med       Date:  2019-11-11       Impact factor: 2.183

4.  MID1 and MID2 regulate cell migration and epithelial-mesenchymal transition via modulating Wnt/β-catenin signaling.

Authors:  Yingying Qiao; Yuan Zhou; Chao Song; Xin Zhang; Yi Zou
Journal:  Ann Transl Med       Date:  2020-08
  4 in total

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