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Search for genetic modifiers of IRF6 and genotype-phenotype correlations in Van der Woude and popliteal pterygium syndromes.
Am J Med Genet A. 2013 Oct; 161A(10):2535-2544.AJ

Abstract

Van der Woude syndrome is the most common form of syndromic orofacial clefting, accounting for 1-2% of all patients with cleft lip and/or cleft palate. Van der Woude and popliteal pterygium syndromes are caused by mutations in IRF6, but phenotypic variability within and among families with either syndrome suggests that other genetic factors contribute to the phenotypes. The aim of this study was to identify common variants acting as genetic modifiers of IRF6 as well as genotype-phenotype correlations based on mutation type and location. We identified an association between mutations in the DNA-binding domain of IRF6 and limb defects (including pterygia). Although we did not detect formally significant associations with the genes tested, borderline associations suggest several genes that could modify the VWS phenotype, including FOXE1, TGFB3, and TFAP2A. Some of these genes are hypothesized to be part of the IRF6 gene regulatory network and may suggest additional genes for future study when larger sample sizes are also available. We also show that families with the Van de Woude phenotype but in whom no mutations have been identified have a lower frequency of cleft lip, suggesting there may be locus and/or mutation class differences in Van de Woude syndrome.

Authors+Show Affiliations

Department of Pediatrics, University of Iowa, Iowa City, IA.Department of Medical Genetics, Mayo Clinic, Rochester, MN.Departments of Microbiology and Molecular Genetics, Pediatrics and Human Development, Michigan State University, East Lansing, MI.Center for Craniofacial and Dental Genetics, Department of Oral Biology, School of Dental Medicine, Department of Human Genetics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, PA.Department of Pediatrics, University of Iowa, Iowa City, IA.Department of Pediatrics, University of Iowa, Iowa City, IA.Department of Pediatrics, University of Iowa, Iowa City, IA.Center for Craniofacial and Dental Genetics, Department of Oral Biology, School of Dental Medicine, Department of Human Genetics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, PA.Department of Pediatrics, University of Iowa, Iowa City, IA.

Pub Type(s)

Journal Article
Research Support, N.I.H., Extramural

Language

eng

PubMed ID

23949966

Citation

Leslie, Elizabeth J., et al. "Search for Genetic Modifiers of IRF6 and Genotype-phenotype Correlations in Van Der Woude and Popliteal Pterygium Syndromes." American Journal of Medical Genetics. Part A, vol. 161A, no. 10, 2013, pp. 2535-2544.
Leslie EJ, Mancuso JL, Schutte BC, et al. Search for genetic modifiers of IRF6 and genotype-phenotype correlations in Van der Woude and popliteal pterygium syndromes. Am J Med Genet A. 2013;161A(10):2535-2544.
Leslie, E. J., Mancuso, J. L., Schutte, B. C., Cooper, M. E., Durda, K. M., L'Heureux, J., Zucchero, T. M., Marazita, M. L., & Murray, J. C. (2013). Search for genetic modifiers of IRF6 and genotype-phenotype correlations in Van der Woude and popliteal pterygium syndromes. American Journal of Medical Genetics. Part A, 161A(10), 2535-2544. https://doi.org/10.1002/ajmg.a.36133
Leslie EJ, et al. Search for Genetic Modifiers of IRF6 and Genotype-phenotype Correlations in Van Der Woude and Popliteal Pterygium Syndromes. Am J Med Genet A. 2013;161A(10):2535-2544. PubMed PMID: 23949966.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Search for genetic modifiers of IRF6 and genotype-phenotype correlations in Van der Woude and popliteal pterygium syndromes. AU - Leslie,Elizabeth J, AU - Mancuso,Jennifer L, AU - Schutte,Brian C, AU - Cooper,Margaret E, AU - Durda,Kate M, AU - L'Heureux,Jamie, AU - Zucchero,Theresa M, AU - Marazita,Mary L, AU - Murray,Jeffrey C, Y1 - 2013/08/15/ PY - 2012/09/13/received PY - 2013/06/14/accepted PY - 2013/8/17/entrez PY - 2013/8/21/pubmed PY - 2014/5/16/medline KW - Van der Woude KW - cleft KW - lip pit KW - modifier gene KW - popliteal pterygium SP - 2535 EP - 2544 JF - American journal of medical genetics. Part A JO - Am J Med Genet A VL - 161A IS - 10 N2 - Van der Woude syndrome is the most common form of syndromic orofacial clefting, accounting for 1-2% of all patients with cleft lip and/or cleft palate. Van der Woude and popliteal pterygium syndromes are caused by mutations in IRF6, but phenotypic variability within and among families with either syndrome suggests that other genetic factors contribute to the phenotypes. The aim of this study was to identify common variants acting as genetic modifiers of IRF6 as well as genotype-phenotype correlations based on mutation type and location. We identified an association between mutations in the DNA-binding domain of IRF6 and limb defects (including pterygia). Although we did not detect formally significant associations with the genes tested, borderline associations suggest several genes that could modify the VWS phenotype, including FOXE1, TGFB3, and TFAP2A. Some of these genes are hypothesized to be part of the IRF6 gene regulatory network and may suggest additional genes for future study when larger sample sizes are also available. We also show that families with the Van de Woude phenotype but in whom no mutations have been identified have a lower frequency of cleft lip, suggesting there may be locus and/or mutation class differences in Van de Woude syndrome. SN - 1552-4833 UR - https://www.unboundmedicine.com/medline/citation/23949966/Search_for_genetic_modifiers_of_IRF6_and_genotype_phenotype_correlations_in_Van_der_Woude_and_popliteal_pterygium_syndromes_ L2 - https://doi.org/10.1002/ajmg.a.36133 DB - PRIME DP - Unbound Medicine ER -