IRF6 rs2235371 as a risk factor for non-syndromic cleft palate only among the Deutero-Malay race in Indonesia and its effect on the IRF6 mRNA expression level

被引:12
作者
Nasroen, Saskia Lenggogeni [1 ]
Maskoen, Ani Melani [2 ]
Soedjana, Hardisiswo [3 ]
Hilmanto, Dany [4 ]
Gani, Basri Abdul [5 ]
机构
[1] Jenderal Achmad Yani Univ, Fac Dent, Dept Oral & Maxillofacial Surg, Bandung, Indonesia
[2] Padjadjaran State Univ, Fac Dent, Dept Oral Biol, Bandung, Indonesia
[3] Padjadjaran State Univ, Fac Med, Dept Surg, Div Plast Surg Reconstruct & Esthet, Bandung, Indonesia
[4] Padjadjaran State Univ, Fac Med, Dept Pediat, Bandung, Indonesia
[5] Syiah Kuala Univ, Fac Dent, Dept Oral Biol, Banda Aceh, Indonesia
关键词
cleft lip and palate; cleft palate; IRF6; rs2235371; IRF6 mRNA expression level; GENE VARIANTS; LIP; ASSOCIATION; POLYMORPHISMS; GENOTYPE;
D O I
10.17219/dmp/142760
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Background During the early embryological development of the face, complex orofacial failure results in a non-syndromic cleft lip and palate (NS CLP). The interferon regulatory factor 6 gene (IRF6) rs2235371 is a non-synonymous polymorphism that is one of the strong candidate genes associated with NS CLP. Objectives The purpose of this study was to determine IRF6 rs2235371 as a risk factor for NS CLP and its phenotypes, including complete unilateral cleft lip and palate (CUCLP), bilateral cleft lip and palate (BCLP), cleft lip only (CL), and cleft palate only (CP), as well as to examine the effect of the polymorphism on the IRF6 mRNA expression levels among the Deutero-Malay race in Indonesia. Material and methods This study used a case-control design and enrolled 264 samples, including 158 NS CLP cases (42 NS CUCLP, 34 NS BCLP, 33 NS CL, and 49 NS CP) and 106 control subjects. DNA was extracted from venous blood, and then subjected to polymerase chain reaction (PCR) and sequencing. The odds ratio (OR) was used to determine the risk factor for NS CLP and its phenotypes. The Livak, Kruskal-Wallis and Mann-Whitney Utests were used to determine mRNA expression levels in the oral epithelium, followed by real-time quantitative PCR (RT-qPCR). Results. Among all of the NS CLP cases, in the NS CP phenotype, OR for the A mutant allele and the GA genotype was 2,492 (p = 0.017) and 2,114 (p = 0.048), respectively. The IRF6 mRNA expression level of the GA genotype was higher in the NS CP subjects as compared to the GG genotype (p = 0.031). Conclusions The IRF6 rs2235371 polymorphism is associated with the NS CP phenotype in Deutero-Malay patients from Indonesia and it affects the IRF6 mRNA expression level.
引用
收藏
页码:59 / 65
页数:7
相关论文
共 32 条
  • [1] IRF6 gene variants in Central European patients with non-syndromic cleft lip with or without cleft palate
    Birnbaum, Stefanie
    Ludwig, Kerstin U.
    Reutter, Heiko
    Herms, Stefan
    de Assis, Nilma A.
    Diaz-Lacava, Amalia
    Barth, Sandra
    Lauster, Carola
    Schmidt, Guel
    Scheer, Martin
    Saffar, Mitra
    Martini, Markus
    Reich, Rudolf H.
    Schiefke, Franziska
    Hemprich, Alexander
    Poetzsch, Simone
    Poetzsch, Bernd
    Wienker, Thomas F.
    Hoffmann, Per
    Knapp, Michael
    Kramer, Franz-Josef
    Noethen, Markus M.
    Mangold, Elisabeth
    [J]. EUROPEAN JOURNAL OF ORAL SCIENCES, 2009, 117 (06) : 766 - 769
  • [2] The complex genetics of cleft lip and palate
    Cobourne, MT
    [J]. EUROPEAN JOURNAL OF ORTHODONTICS, 2004, 26 (01) : 7 - 16
  • [3] The PAX1 locus at 20p11 is a potential genetic modifier for bilateral cleft lip
    Curtis, Sarah W.
    Chang, Daniel
    Lee, Myoung Keun
    Shaffer, John R.
    Indencleef, Karlijne
    Epstein, Michael P.
    Cutler, David J.
    Murray, Jeffrey C.
    Feingold, Eleanor
    Beaty, Terri H.
    Claes, Peter
    Weinberg, Seth M.
    Marazita, Mary L.
    Carlson, Jenna C.
    Leslie, Elizabeth J.
    [J]. HUMAN GENETICS AND GENOMICS ADVANCES, 2021, 2 (02):
  • [4] Freitas JAD, 2012, J APPL ORAL SCI, V20, P9
  • [5] A Novel Van der Woude Syndrome-CausingIRF6Variant Is Subject to Incomplete Non-sense-Mediated mRNA Decay Affecting the Phenotype of Keratinocytes
    Degen, Martin
    Girousi, Eleftheria
    Feldmann, Julia
    Parisi, Ludovica
    La Scala, Giorgio C.
    Schnyder, Isabelle
    Schaller, Andre
    Katsaros, Christos
    [J]. FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY, 2020, 8
  • [6] Cleft lip and palate: understanding genetic and environmental influences
    Dixon, Michael J.
    Marazita, Mary L.
    Beaty, Terri H.
    Murray, Jeffrey C.
    [J]. NATURE REVIEWS GENETICS, 2011, 12 (03) : 167 - 178
  • [7] Accuracy of haplotype frequency estimation for biallelic loci, via the expectation-maximization algorithm for unphased diploid genotype data
    Fallin, D
    Schork, NJ
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2000, 67 (04) : 947 - 959
  • [8] The complex role of genetic background in shaping the effects of spontaneous and induced mutations
    Goldstein, Ilan
    Ehrenreich, Ian M.
    [J]. YEAST, 2021, 38 (03) : 187 - 196
  • [9] Genetic factors define CPO and CLO subtypes of nonsyndromicorofacial cleft
    Huang, Lulin
    Jia, Zhonglin
    Shi, Yi
    Du, Qin
    Shi, Jiayu
    Wang, Ziyan
    Mou, Yandong
    Wang, Qingwei
    Zhang, Bihe
    Wang, Qing
    Ma, Shi
    Lin, He
    Duan, Shijun
    Yin, Bin
    Lin, Yansong
    Wang, Yiru
    Jiang, Dan
    Hao, Fang
    Zhang, Lin
    Wang, Haixin
    Jiang, Suyuan
    Xu, Huijuan
    Yang, Chengwei
    Li, Chenghao
    Li, Jingtao
    Shi, Bing
    Yang, Zhenglin
    [J]. PLOS GENETICS, 2019, 15 (10):
  • [10] RETRACTED: Epidemiological characteristic of Orofacial clefts and its associated congenital anomalies: retrospective study (Retracted article. See vol. 23, 2023)
    Impellizzeri, A.
    Giannantoni, I.
    Polimeni, A.
    Barbato, E.
    Galluccio, G.
    [J]. BMC ORAL HEALTH, 2019, 19 (01)