Skip to main content

Advertisement

Log in

Sequencing of the interferon regulatory factor 6 (IRF6) gene and correlation to its phenotypes in familial non-syndromic cleft lip and palate in North Indian population

  • Original Paper
  • Published:
European Journal of Plastic Surgery Aims and scope Submit manuscript

Abstract

Background

The incidence of orofacial clefting varies depending upon geographical location, ethnicity, sex and even socioeconomic status. The study aimed to test the contribution of interferon regulatory factor 6 (IRF6) gene allelic variation to the incidence of non-syndromic cleft lip and/or cleft palate (CL/P) from the population of North India.

Methods

Patients from 12 North Indian families with non-syndromic cleft lip with or without cleft palate (NSCL/P) with at least two members affected were clinically evaluated and tested. DNA was extracted from the blood, and three exonic part of the IRF6 gene (exons 2, 5 and 7) were amplified by PCR. Direct sequencing was performed by PCR product, and sequencing results were compared with the reference DNA sequence of the IRF6 gene.

Results

Three SNPs (rs861019, rs2013162 and rs2235372) in 4 out of 12 families were observed. SNP rs861019 was detected in family no. 4 (F4) around exon 2, SNP 2013162 was detected in family no. 10 (F10) and SNP 2235372 was detected in family nos. 5 and 9 (F5 and F9).

Conclusions

This study demonstrates that the three SNPs within the IRF6 gene are associated with NSCL/P, suggesting IRF6 gene sequence variability and variation in this gene, providing first genetic clue to the NSCL/P phenotype in North Indian families. This is our initial step to demonstrate the involvement of the IRF6 gene in NSCL/P patients in North India. Further extensive study and statistical analysis are needed to validate our result.

Level of Evidence: Level IV, diagnostic study.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3

Similar content being viewed by others

References

  1. Marazita ML, Mooney MP (2004) Current concepts in the embryology and genetics of cleft lip and cleft palate. Clin Plast Surg 31(2):125–140

    Article  PubMed  Google Scholar 

  2. Croen LA, Shaw GM, Jensvold NG, Harris JA (1991) Birth defects monitoring in California: a resource for epidemiological research. Paediatr Perinat Epidemiol 5:423–27

    Article  CAS  PubMed  Google Scholar 

  3. Ankola AV, Nagesh L, Hegde P, Karibasappa (2005) Primary dentition status and treatment needs of children with cleft lip and/or palate. J Indian Soc Pedod Prev Dent 23:80–82

    Article  PubMed  Google Scholar 

  4. Murthy J, Bhaskar L (2009) Current concepts in genetics of nonsyndromic clefts. Indian J Plast Surg 42:68–81

    Article  PubMed Central  PubMed  Google Scholar 

  5. Schutte BC, Murray JC (1999) The many faces and factors of orofacial clefts. Hum Mol Genet 8:1853–1859

    Article  CAS  PubMed  Google Scholar 

  6. Mitchell LE, Risch N (1992) Mode of inheritance of nonsyndromic cleft lip with or without cleft palate. Am J Hum Genet 51(2):323–332

    CAS  PubMed Central  PubMed  Google Scholar 

  7. Wyszynski DF, Beaty TH (1996) Review of the role of potential teratogens in the origin of human nonsyndromic oral clefts. Teratology 53(5):309–317

    Article  CAS  PubMed  Google Scholar 

  8. Cobourne MT (2004) The complex genetics of cleft lip and palate. Eur J Orthod 26:7–16

    Article  PubMed  Google Scholar 

  9. Jugessur A, Murray JC (2005) Orofacial clefting: recent insights into a complex trait. Curr Opin Genet Dev 15:270–278

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  10. Stanier P, Moore GE (2004) Genetics of cleft lip and palate: syndromic genes contribute to the incidence of non-syndromic clefts. Hum Mol Genet 1:13

    Google Scholar 

  11. Schutte BC, Sander A, Malik M, Murray JC (1996) Refinement of the Van der Woude gene location and construction of a 3.5-Mb YAC contig and STS map spanning the critical region in 1q32-q41. Genomics 36(3):507–514

    Article  CAS  PubMed  Google Scholar 

  12. Janku P, Robinow M, Kelly T, Bralley R, Baynes A, Edgerton MT et al (1980) The van der Woude syndrome in a large kindred: variability, penetrance, genetic risks. Am J Med Genet 5:117–123

    Article  CAS  PubMed  Google Scholar 

  13. Shprintzen RJ, Goldberg RB, Sidoti EJ (1980) The penetrance and variable expression of the Vander Woude syndrome: implications for genetic counseling. Cleft Palate J 17(1):52–57

    CAS  PubMed  Google Scholar 

  14. Ranta R, Rintala AE (1983) Correlations between microforms of the Van der Woude syndrome and cleft palate. Cleft Palate J 20(2):158–162

    CAS  PubMed  Google Scholar 

  15. Kondo S, Schutte BC, Richardson RJ, Bjork BC, Knight AS, Watanabe Y et al (2002) Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes. Nat Genet 32(2):219–220

    Article  Google Scholar 

  16. Wang X, Liu J, Zhang H, Xiao M, Li J, Yang C et al (2003) Novel mutations in the IRF6 gene for Van der Woude syndrome. Hum Genet 113:382–386

    Article  CAS  PubMed  Google Scholar 

  17. Kayano S, Kure S, Suzuki Y, Kanno K, Aoki Y, Kondo S et al (2003) Novel IRF6 mutations in Japanese patients with Van der Woude Syndrome: two missense mutations (R45Q and P396S) and a 17-kb deletion. Hum Genet 48:622–628

    Article  CAS  Google Scholar 

  18. NCBI (2011) Single nucleotide polymorphism, NCBI database (dbSNP), build 126. http://www.ncbi.nlm.nih.gov/pro-jects/SNP/index.html. Accessed 12 Jan 2011

  19. Ensembl (2011) Ensembl genome browser. http://www.ensembl.org/index.htm. Accessed 12 Jan 2011

  20. EMBL-EBI (2011) Multiple sequence alignment programs for DNA or proteins. http://www.ebi.ac.uk/Tools/msa/clustalw2/. Accessed 12 Jan 2011

  21. Zucchero TM, Cooper ME, Maher BS, Daack-Hirsch S, Nepomu-ceno B, Ribeiro L et al (2004) Interferon regulatory factor 6 (IRF6) gene variants and the risk of isolated cleft lip or palate. N Engl J Med 351:769–780

    Article  CAS  PubMed  Google Scholar 

  22. Blanton SH, Cortez A, Stal S, Mulliken JB, Finnell RH, Hecht JT (2005) Variation in IRF6 contributes to nonsyndromic cleft lip and palate. Am J Med Genet 137A:259–262

    Article  PubMed  Google Scholar 

  23. Ghassibé M, Bayet B, Revencu N, Verellen-Dumoulin C, Gillerot Y, Vanwijck R et al (2005) Interferon regulatory factor-6: a gene predisposing to isolated cleft lip with or without cleft palate in the Belgian population. Eur J Hum Genet 13:1239–1242

    Article  PubMed  Google Scholar 

  24. Park JW, Mcintosh I, Hetmanski JB, Jabs EW, Vander Kolk CA, Craig A et al (2007) Association between IRF6 and nonsyndromic cleft lip with or without cleft palate in four populations. Genet Med 9:219–227

    Article  PubMed Central  PubMed  Google Scholar 

  25. Scapoli L, Palmieri A, Martinelli M, Pezzetti F, Carinci P, Tognon M et al (2005) Strong evidence of linkage disequilibrium between polymorphisms at the IRF6 locus and nonsyndromic cleft lip with or without cleft palate, in an Italian population. Am J Hum Genet 76:180–183

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  26. Srichomthong C, Siriwan P, Shotelersuk V (2005) Significant association between IRF6 820G > A and non-syndromic cleft lip with or without cleft palate in the Thai population. J Med Genet 42:e46

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  27. Morkūnienė A, Steponavičiūtė D, Kasnauskienė J, Kučinskas V (2006) Nucleotide sequence changes in the MSX1 and IRF6 genes in Lithuanian patients with nonsyndromic orofacial clefting. Acta Med Lituanica 13(4):219–225

    Google Scholar 

  28. Pegelow M, Peyrard-Janvid M, Zucchelli M, Fransson I, Larson O, Kere J, Larsson C et al (2008) Familial non-syndromic cleft lip and palate—analysis of the IRF6 gene and clinical phenotypes. Eur J Orthod 30:169–175

    Article  CAS  PubMed  Google Scholar 

  29. Diercks GR, Karnezis TT, Kent DT, Flores C, Su GH, Lee JH, Haddad J Jr (2009) The association between interferon regulatory factor 6 (IRF6) and nonsyndromic cleft lip with or without cleft palate in a Honduran population. Laryngoscope 119(9):1759–1764

    Article  CAS  PubMed  Google Scholar 

  30. Larrabee YC, Birkeland AC, Kent DT, Flores C, Su GH, Lee JH, Haddad J Jr (2011) Association of common variants, not rare mutations, in IRF6 with nonsyndromic clefts in a Honduran population. Laryngoscope 121(8):1756–1759

    Article  CAS  PubMed  Google Scholar 

Download references

Acknowledgments

We are grateful to the family members for their participation in this study, to the staff of the Department of Orthodontics and Dentofacial Orthopedics, BBDCODS, Lucknow and Shushrut Institute of Plastic Surgery Hospital, Lucknow. We also would like to thank the Department of Molecular Bioprospection, Central Institute of Medicinal and Aromatic Plants (CSIR) for taking keen interest in this research topic.

Conflict of interest

None

Ethical standards

This study has been approved by the appropriate ethics committee and have therefore been performed in accordance with the ethical standards laid down in the 1964 Declaration of Helsinki and its later amendments. All persons gave their informed consent prior to their inclusion in this study.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Rohit Khanna.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Khanna, R., Tikku, T., Jain, G.S. et al. Sequencing of the interferon regulatory factor 6 (IRF6) gene and correlation to its phenotypes in familial non-syndromic cleft lip and palate in North Indian population. Eur J Plast Surg 37, 319–326 (2014). https://doi.org/10.1007/s00238-014-0937-5

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00238-014-0937-5

Keywords

Navigation