AJMB

Association of AIRE Polymorphism and the Susceptibility to Multiple Sclerosis in Iranian Population

PDF - Export to EndNote - PubMed Central XML format - PubMed Central XML format - PubMed Central XML format
PMID: 29849988 (PubMed) - PMCID: PMC5960056 - View online: PubReader
Volume 10, Issue 2, April-June , Page 110 to 114
Saturday, February 4, 2017 :Received , Wednesday, April 19, 2017 :Accepted


  • - Department of Pharmaceutical Biotechnology, Faculty of Pharmacy, Isfahan University of Medical Sciences, Isfahan, Iran
  • Corresponding author Department of Immunology, Faculty of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran, Tel: +98 31 37929136, E-mail: Alsahebfosoul@med.mui.ac.ir
    - Department of Immunology, Faculty of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran

  • - Department of Genetics and Molecular Biology, Faculty of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran

  • - Department of Genetics and Molecular Biology, Faculty of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran

  • - Department of Pharmaceutical Biotechnology, Faculty of Pharmacy, Isfahan University of Medical Sciences, Isfahan, Iran

Abstract:

Background: Multiple Sclerosis (MS) is the most common cause of neurologic disability in young adults. Recently, the AIRE gene was identified as a genetic risk factor for several autoimmune diseases in genome wide association studies. The aim of this study was to further investigate the possible role of the AIRE gene in susceptibility to MS in Iranian population.
Methods: A total of 112 MS patients and 94 ethnically matched controls were included in the study. The Single-Nucleotide Polymorphism (SNP) (rs1800520, C>G) with a global MAF=0.2282/1143 was selected and genotyped using HRM real-time PCR method.
Results: Results showed that AIRE SNP rs1800520 was significantly less common in the MS patients than in healthy controls (17.8 vs. 28.7%, pc=0.032, OR=0.54,95% CI 0.279,1.042). Also, the frequency of allele G was significantly higher among the control group than in the case group (37.77 vs. 25%, pc=0.014). Interestingly, mRNA transcribed on the rs1800520 SNP showed decreased free energy than the wild type suggesting that its increased stability may be responsible for the different activities of the polymorphic AIRE molecule. 
Conclusions: This is the first study investigating the relationship between AIRE gene and the susceptibility to MS. These results indicated that the rs1800520 SNP is not a susceptibility gene variant for the development of MS in Iranian population.


 

 

Introduction :

Multiple Sclerosis (MS) is an autoimmune, common and severe CNS disease that is characterized by demyelination, chronic inflammation, axonal and oligodendrocyte pathology, and progressive neurological dysfunction 1. Prevalence rates for MS vary between 2 and 160 per 100,000 in different countries, and more than 2 million individuals are affected by this disease worldwide 2. The incidence and prevalence of MS in Iran has been increasing rapidly, especially in females 3. Extensive epidemiological data confirm that genetic variation is an important determinant of susceptibility to MS, and suggest that such variation also influences the timing of symptom onset, the course of the disease, and the treatment response 4. MS as an autoimmune disease is caused by a breakdown in central or peripheral tolerance toward self-antigens, allowing autoreactive pathogenetic T and B cells clones arising, and a complex mix of genetic and environmental factors is believed to mediate this breakdown 5-7. The co-occurrence of autoimmune diseases in the same individual has prompted several studies aimed to recognize shared pathophysiological mechanisms. 
Among genetic factors, variant of AIRE (Autoimmune Regulator) gene has been correlated with autoimmune manifestations in the APECED 8,9, rheumatoid arthritis 10,11, the immune deficiency omenn syndrome 12, alopecia aerate 13, and lupus like panniculitis in patients with APECED 14 but not with type I diabetes, addison disease 15 and Graves’ disease 16, myasthenia gravis 17 as well as inflammatory bowel disease 18. AIRE protein acts as a powerful transcriptional transactivator. The AIRE protein, mostly localized in the cell nucleus, is composed by specific domains including the amino-terminal HSR domain, the Nuclear Localization Signal (NLS), the Sp100, AIRE1, nucP41/75, DEAF 1 (SAND) domain, two Plan the Homeodomain (PHD) type zinc fingers, and four LXXLL motifs 19. The highest level of AIRE expression is in thymus where it is seen in a subpopulation of modularly Thymic Epithelial Cells (mTEC) 4. In mTECs, AIRE is required for the expression of many Tissue-Restricted self-Antigens (TRAs) 20. The expression of TRAs in mTECs allows the negative selection of autoreactive lymphocytes. In the absence of functional AIRE, human patients and mice develop multi-organ autoimmune disease due to a defect in thymic negative selection 21.
On this basis, an attempt was made to analyze SNP rs1800520 in the SAND domain of AIRE gene in order to investigate whether this polymorphic genotype could protect or predispose to the development of MS. Among all the AIRE SNPs already identified, this SNP was selected following three main criteria concluding: 1) the SAND domain is a conserved sequence motif in nuclear proteins including Sp100 family and plays a key role in transcription regulation, thus mutations at this domain could destabilize the binding of AIRE to TRAs promoter and lower TRAs expression in thymic epithelial cells 22; 2) the already demonstrated association of this SNP with human autoimmune diseases specially rheumatoid arthritis in which Genome-Wide Association Studies (GWAS) on rheumatoid arthritis and MS show that these diseases share many genetic factors 23 and 3) the only common frequency (MAF>0.05) SNP leading to a mis-sense mutation (serine to arginine) in AIRE exon and the MAF of this SNP in Asian population is 0.475 17.

 

Materials and Methods :

Study subjects: A total of 112 MS patients (87 women and 25 men) were included in the study. All patients met the MS research center of the Alzahra hospital in Isfahan, Iran. The control population consisted of 94 healthy persons without any autoimmune diseases. Demographic information of patient and control population was presented in supplementary data. Blood samples were obtained from subjects after they provided written informed consent. Genomic DNA was extracted from blood leukocytes using QIAmpDNA Mini Kit (Qiagen, Hilden, Germany) according to the manufacturer’s recommendations and stored at -20oC.
SNP genotyping: The polymorphism rs1800520 (C8723G) was investigated using the allelic discrimination assay by HRM-real time PCR. PCR was performed using two primers flanking the SNP. The assay was conducted with the Rotor-Gene 6000 instrument (Corbett Life Science) and the software Rotor-Gene 6000 series version 1.7 was used to analyze the results. PCR was carried out in three steps: activation, amplification and melting. Primer sequences and HRM-real time PCR conditions were listed in table 1. At least, 10% of all genotyping results were confirmed by sequencing.
Prediction of RNA secondary structures of AIRE allelic variants: The potential variations in folding of the RNA secondary structure caused by the SNP rs1800520 of AIRE variants were identified using the RNA structure web servers on the Mathews Lab Web Servers from University of Rochester Medical Center (http://rna.urmc.rochester.edu/).
Statistical analysis: SPSS (version 18.0, SPSS, Chicago, IL, USA) was used for statistical analysis. Statistically significant differences between genotype frequencies were assessed using univariate analyses such as the Fisher's exact test for binary variables and the Student t test for continuous variables. The association between the presence of polymorphic genotypes and independent variables was studied using a multivariate logistic regression analysis. The genotype and allelic frequencies were assessed using the Hardy-Weinberg equilibrium (https://www.easycalculation.com/health/hardy-weinberg-equilibrium-calculator.php). Odds Ratio (ORs) and 95% Confidence Intervals (95% CIs) were calculated and p-values lower than 0.05 were considered statistically significant.

 

Results :

Decreased frequency of rs1800520 (C8723G) SNP in MS patients compared with controls: Analysis of the polymorphism rs1800520 genotype and allelic frequencies showed that both groups (patients and controls) were in Hardy-Weinberg equilibrium. The genotype and allelic frequencies were re-analyzed by SNPStat software and recessive form was selected as the best model according to the AIC (Table 2). Results demonstrated that AIRE SNP rs1800520 was significantly less common in the MS patients than in healthy controls (17.9% vs. 29%, pc = 0.032, OR = 0.54, 95% CI 0.279, 1.04)(Table 3).
Stratification of the frequency of rs1800520 SNP for age of MS onset and sex: Dependency of the frequency of rs1800520 (C8723G) on independent variables such as sex and age of MS onset was investigated on the patient and control population. For the frequency of rs1055311 (C8385T) SNP, there was no statistically significant difference in males in comparison to females in the patient and control groups and also no significant associations of the tested SNP with sex and age of MS onset were detected in the patient group (Table 4).
AIRE polymorphism and mRNA structure: In order to characterize the mechanisms determining the different functional activity of AIRE allelic variants at the molecular level, our analysis was focused on mRNA folding structure. Genetic polymorphisms may generate mRNA molecules showing different secondary structures. Interestingly, variants of mRNA secondary structure have been associated with different efficiencies of gene expression depending on the free energy possessed by the single mRNA molecule 18. Therefore, the mRNA folding structure corresponding to the AIRE allelic non-synonymous variants AGCG, present in the wild-type genotype, and AGGG, present in the rs1800520 (C8723G) SNP, in exon 7 was investigated using the RNA structure web servers on the Mathews Lab Web Servers from University of Rochester Medical Center (http://rna.urmc.rochester.edu/). mRNA transcribed on AIRE AGCG allele showed lower free energy (dG=-1043.5 kcal/mol) than the one transcribed on the AGGG allele (dG=-1404.5 kcal/mol), suggesting that the latter likely has greater molecular stability than the former (Figures 1A and 1B). In conclusion, mRNA molecules transcribed on the variant AGGG genotype might have a longer half-life and produce more AIRE protein than mRNA molecules transcribed on the wild type AGCG genotype.

 

Discussion :

AIRE is a transcriptional regulator and is expressed primarily by medullary thymic epithelial cells and cells of the monocytes dendritic cell lineage of the thymus. The expression of AIRE in non-thymic tissues is still controversial 24. AIRE plays a major role in thymocyte education and negative selection by controlling the expression of peripheral antigens in the thymus 25. Thus, AIRE is a good functional candidate in autoimmune diseases regardless of the population. In fact, mutations in this gene cause autoimmune polyendocrinopathy candidiasis-ectodermal dystrophy (APECED), which is one of the few known monogenic autoimmune diseases where patients suffer from both endocrine and non-endocrine manifestations. AIRE mutations and polymorphisms have been found in different autoimmune manifestations correlated or not correlated to APECED 26.
In this research, SNP rs1800520 (C>G) of AIRE gene was analyzed in the MS patients in Iranian population. TheS278R replacement by rs1800520 is located in the SAND domain, a conserved sequence motif in nuclear proteins and plays a key role in transcription regulation. AIRE SNPs have been positively correlated with some autoimmune diseases and some researchers have investigated SNP rs1800520 with respect to Finnish type 1 diabetes 27, rheumatoid arthritis 10,11, melanoma 20, myasthenia gravis 17 and APS1 28. The GWA study of Terao et al established the association of SNP rs1800520 with rheumatoid arthritis in the Japanese population but García-Lozano et al observed no significant difference in the distribution of the G allele of rs1800520 between rheumatoid arthritis patients and controls in the European population. Conteduca et al found that this SNP was significantly more frequent in healthy subjects than in melanoma patients, independently from sex, age and stages of melanoma and concluded that G allele exerts a significant protective effect against melanoma. Zhang et al showed that there were no significant differences in frequencies of alleles and genotypes in rs1800520 between myasthenia gravis group and the control group in the Chinese population. Also Turunen et al found that this SNP does not seem to contribute to disease susceptibility in Finnish type 1 diabetic patients.
Our study is the first study on the correlation of AIRE polymorphism and MS. The increased frequency of rs1800520 (C8723G) SNP in healthy subjects with respect to MS patients suggests that this polymorphism may be associated with an increased expression of AIRE in individuals bearing the corresponding genotypes (GG), thus conferring them a potential protecting against MS development. Our in silico analysis of the folding of the polymorphic AIRE mRNA structures showed that the genotype corresponding to rs1800520 SNP leads to the transcription of a mRNA molecule whose secondary structure is likely more stable than the one of the mRNA coded by the AIRE wild-type genotype. This observation suggests that, in the case ofrs1800520 SNP, AIRE mRNA may have a longer half-life causing increased AIRE protein production and, thereby, leading to higher MS-associated antigen expression in mTECs and negative selection of autoreactive lymphocytes. Further studies are warranted to validate these results and to investigate the underlying molecular mechanisms because the increased frequency of this SNP was shown in many autoimmune diseases. Thus, our results may demonstrate the lack of association between this SNP and MS in Iranian population and may associate MS susceptibility with another AIRE SNPs or the same SNP in another population like RA susceptibility association with this SNP in Japanese population but not in European population 10,11.

 

Acknowledgement :

We thank Dr. Mansour Salehi, Dean of Genome Laboratory located in the Isfahan City, for generously allowing us to use his laboratory equipment.

 

Conflict of Interest :

The authors report no conflicts of interest. The authors alone are responsible for the content and writing of the paper.

 



<p>Figure 1. Computerized modeling of AIRE mRNA structures of two haplotype variants in exon 7. A) AGCG allelic variant corresponding to the wild-type genotype; B) AGGG allelic variant corresponding to the C8723G SNP.</p>

Figure 1. Computerized modeling of AIRE mRNA structures of two haplotype variants in exon 7. A) AGCG allelic variant corresponding to the wild-type genotype; B) AGGG allelic variant corresponding to the C8723G SNP.


<p>Table 1. Primer sequences and PCR conditions</p>

Table 1. Primer sequences and PCR conditions


<p>Table 2. Selection of the best model by SNPstat software</p> <p>*Odds Ratio, **Confidence Interval, *** Akaike Information Criterion, **** Bayesian Information Criterion.</p>

Table 2. Selection of the best model by SNPstat software

*Odds Ratio, **Confidence Interval, *** Akaike Information Criterion, **** Bayesian Information Criterion.


<p>Table 3. Allele and genotype frequency of AIRE rs1800520</p> <p>*Odds Ratio, **Confidence Interval.</p>

Table 3. Allele and genotype frequency of AIRE rs1800520

*Odds Ratio, **Confidence Interval.


<p>Table 4. Association of the SNP rs1800520 with the sex and age of MS onset</p> <p>*Odds Ratio, **Confidence Interval.</p>

Table 4. Association of the SNP rs1800520 with the sex and age of MS onset

*Odds Ratio, **Confidence Interval.


References :
  1. Kidd PM. Multiple sclerosis, an autoimmune inflammatory disease: prospects for its integrative management. Altern Med Rev 2001;6(6):540-566.   [PubMed]
  2. Hoffjan. S, Akkad DA. The genetics of multiple sclerosis: sn update 2010. Mol Cell Probes 2010;24(5):237-243.   [PubMed]
  3. Etemadifar M, Abtahi SH. Multiple sclerosis in Isfahan: past, present and future. Int J Prev Med 2012;3(5):301-302.   [PubMed]
  4. Oksenberg JR, Baranzini SE. Multiple sclerosis genetics--is the glass half full, or half empty? Nat Rev Neurol 2010;6(8):429-437.   [PubMed]
  5. Su MA, Anderson MS. Aire: an update. Curr Opin Immunol 2004;16(6):746-752.   [PubMed]
  6. Pender MP, Greer JM. Immunology of multiple sclerosis. Curr Allergy Asthma Rep 2007;7(4):285-292.   [PubMed]
  7. Korn T. Pathophysiology of multiple sclerosis. J Neurol 2008;255(Suppl 6):2-6.   [PubMed]
  8. Björses P, Aaltonen J, Horelli-Kuitunen N, Yaspo ML, Peltonen L. Gene defect behind APECED: a new clue to autoimmunity. Hum Mol Genet 1998;7(10):1547-1553.   [PubMed]
  9. Ishii T, Suzuki Y, Ando N, Matsuo N, Ogata T. Novel mutations of the autoimmune regulator gene in two siblings with autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy. J Clin Endocrinol Metab 2000;85(8):2922-2926.   [PubMed]
  10. García-Lozano JR, Torres-Agrela B, Montes-Cano MA, Ortiz-Fernández L, Conde-Jaldón M, Terue M, et al. Association of the AIRE gene with susceptibility to rheumatoid arthritis in a European population: a case control study. Arthritis Res Ther 2013;15(1):R11.   [PubMed]
  11. Terao C, Yamada R, Ohmura K, Takahashi M, Kawaguchi T, Kochi Y, et al. The human AIRE gene at chromosome 21q22 is a genetic determinant for the predisposition to rheumatoid arthritis in Japanese population. Hum Mol Genet 2011;20(13):2680-2685.   [PubMed]
  12. Cavadini P, Vermi W, Facchetti F, Fontana S, Nagafuchi S, Mazzolari E, et al. AIRE deficiency in thymus of 2 patients with Omenn syndrome. J Clin Invest 2005;115(3):728-732.   [PubMed]
  13. Tazi-Ahnini R, Cork MJ, Gawkrodger DJ, Birch MP, Wengraf D, McDonagh AJ, et al. Role of the autoimmune regulator (AIRE) gene in alopecia aureate: strong association of a potentially functional AIRE polymorphism with alopecia universalis. Tissue Antigens 2002;60(6):489-495.   [PubMed]
  14. Füchtenbusch M, Vogel A, Achenbach P, Gummer M, Ziegler AG, Albert E, et al. Lupus-like panniculitis in a patient with autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED). Exp Clin Endocrinol Diabetes 2003;111(5):288-293.   [PubMed]
  15. Tait KF, Gough SC. The genetics of autoimmune endocrine disease. Clin Endocrinol (Oxf) 2003;59(1):1-11.   [PubMed]
  16. Colobran R, Giménez-Barcons M, Marín-Sánchez A, Porta-Pardo E, Pujol-Borrell R. AIRE genetic variants and predisposition to polygenic autoimmune disease: The case of Graves’ disease and a systematic literature review. Hum Immunol 2016;77:643-651.   [PubMed]
  17. Zhang X, Ding XJ, Wang Q, Yue YX, Xie Y, Hao HJ, et al. Rs3761389 polymorphism in autoimmune regulator (AIRE) gene is associated with susceptibility of myasthenia gravis in Chinese patients. J Clin Neurosci 2017;40:180-184.   [PubMed]
  18. Török HP, Tonenchi L, Glas J, Schiemann U, Folwaczny C. No significant association between mutations in exons 6 and 8 of the autoimmune regulator (AIRE) gene and inflammatory bowel disease. Eur J Immunogenet 2004;31(2):83-86.   [PubMed]
  19. De Martino L, Capalbo D, Improda N, D'Elia F, Di Mase R, D'Assante R. APECED: a paradigm of complex interactions between genetic background and susceptibility factors. Front Immunol 2013;4:331.   [PubMed]
  20. Conteduca G, Ferrera F, Pastorino L, Fenoglio D, Negrini S, Sormani MP, et al. The role of AIRE polymorphisms in melanoma. Clin Immunol 2010;136:96-104.   [PubMed]
  21. Taniguchi RT, Anderson MS. The role of Aire in clonal selection. Immunol Cell Biol 2011;89(1):40-44.   [PubMed]
  22. Waterfield M, Khan IS, Cortez JT, Fan U, Metzger T, Greer A, et al. The transcriptional regulator Aire coopts the repressive ATF7ip-MBD1 complex for the induction of immunotolerance. Nat Immunol 2014;15:258-265.   [PubMed]
  23. Suzuki A, Kochi Y, Okada Y, Yamamoto K. Insight from genome-wide association studies in rheumatoid arthritis and multiple sclerosis. FEBS Lett 2011;585:3627-3632.   [PubMed]
  24. Rizzi M, Ferrera F, Filaci G, Indiveri F. Disruption of immunological tolerance: role of AIRE gene in autoimmunity. Autoimmun Rev 2006;5:145-147.   [PubMed]
  25. Abramson J, Giraud M, Benoist C, Mathis D. AIRE 's partners in the molecular control of immunological tolerance. Cell 2010;140(1):123-135.   [PubMed]
  26. Bruserud Ø,Oftedal BE, Wolff AB, Husebye ES. AIRE-mutations and autoimmune disease. Curr Opin Immunol 2016;43:8-15.   [PubMed]
  27. Turunen JA, Wessman M, Forsblom C, Kilpikari R, Parkkonen M, PontynenN, et al. Association analysis of the AIRE and insulin genes in Finnish type 1 diabetic patients. Immunogenetics 2006;58(5-6):331-338.   [PubMed]
  28. Faiyaz-Ul-Haque M, Bin-Abbas B, Al-Abdullatif A, Abdullah Abalkhail H, Toulimat M, Al-Gazlan S, et al. Novel and recurrent mutations in the AIRE gene of autoimmune polyendocrinopathy syndrome type 1 (APS1) patients. Clin Genet 2009;76(5):431-440.   [PubMed]