Associations of genetic variants in endocytic trafficking of epidermal growth factor receptor super pathway with risk of nonsyndromic cleft lip with or without cleft palate

Mol Genet Genomic Med. 2018 Nov;6(6):1157-1167. doi: 10.1002/mgg3.497. Epub 2018 Nov 8.

Abstract

Background: The genetic etiology of nonsyndromic cleft lip with or without cleft palate (NSCL/P) has not been fully clarified to date. Epidermal growth factor receptor (EGFR) was reportedly involved in its biological establishment and regulation of cell migration during the embryonic stage.

Methods: We selected a super pathway of endocytic trafficking of EGFR and investigated the associations of single-nucleotide polymorphisms (SNPs) in the super pathway with the risk of NSCL/P by analyzing our published genome-wide association study (GWAS) data from 504 NSCL/P individuals and 455 controls. After the false discovery rate (FDR) control, we conducted linkage disequilibrium (LD) analyses and conditional regression analyses to obtain independent lead SNPs. We performed LD analyses between the lead SNPs and the reported SNPs to find novel ones from our study. We annotated the lead SNPs and investigated their mapped genes in silico.

Results: A total of 82 SNPs showed a statistical association with the risk of NSCL/P after FDR control. They contained three reported SNPs which were g.117068049G>A (rs7078160), g.117086783C>G (rs10886040), and g.117101266G>T (rs17095681). Four independent lead SNPs were obtained, including g.116979803 T>C (rs1905539) and g.117037960A>G (rs7902502) at 10q25.3, g.35720163G>C (rs75656820) at 17q12, and g.156864512G>A (rs1800877) at 1q23.1. Three of them were in low LD (r2 < 0.5) with the reported SNPs except g.117037960A>G (rs7902502), so these three were newly identified. Lead SNPs were mapped to three genes: SHTN1, AP2B1, and NTRK1. The three genes were relatively more highly expressed in the human craniofacial region and in the proximal maxillary location during the craniofacial development stage of the embryonic mouse.

Conclusion: Our results suggested that SHTN1, AP2B1, and NTRK1 might be associated with the development of NSCL/P.

Keywords: endocytosis; epidermal growth factor receptor; genome-wide association study; nonsyndromic cleft lip with or without cleft palate; pathway; single-nucleotide polymorphism.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptor Protein Complex beta Subunits / genetics*
  • Carrier Proteins / genetics*
  • Case-Control Studies
  • Cleft Lip / genetics*
  • Cleft Lip / pathology
  • Cleft Palate / genetics*
  • Cleft Palate / pathology
  • Cytoskeletal Proteins
  • Humans
  • Linkage Disequilibrium
  • Polymorphism, Single Nucleotide*
  • Receptor, trkA / genetics*

Substances

  • AP2B1 protein, human
  • Adaptor Protein Complex beta Subunits
  • Carrier Proteins
  • Cytoskeletal Proteins
  • SHTN1 protein, human
  • Receptor, trkA

Associated data

  • GENBANK/NC_000010.11
  • GENBANK/NC_000017.11
  • GENBANK/NC_000001.11