Association of novel polymorphisms in TMEM39A gene with systemic lupus erythematosus in a Chinese Han population

Systemic lupus erythematosus (SLE) is typically characterized by the dysregulation of T cell response and B cell activation which usually causes the formation of immune complexes in multiple organs and tissues [1]. Although the pathogenesis of SLE is largely unknown to date, it most likely involves environmental and genetic factors. Several candidate-gene studies and genome-wide association (GWA) scans have successfully discovered multiple susceptibility genes that fall into key pathways implicating immune complex clearance, immune signal transduction and interferon pathways contributing to the development of SLE [2, 3]. However, much of the heritable risk needs to be identified.

Recently, multiethnic approach was utilized to find that three SLE risk loci exceeded the genome-wide significance threshold, including interferon regulatory factor 8 (IRF8), transmembrane protein 39A (TMEM39A), and 17q21 between IKAROS family of zinc finger 3 (IKZF3) and zona pellucida binding protein 2 (ZPBP2) [4]. The 17q21 region was originally associated with asthma in family linkage study [5‐7]. More single nucleotide polymorphisms (SNPs) in the 17q21 region have been identified as being associated with the susceptibility to autoimmune diseases, including rheumatoid arthritis, ankylosing spondylitis and SLE [4, 8‐10]. IRF8 is a family member of transcription factors that play a critical role in the regulation of cell apoptosis and immune response [11]. It is required for promoting type I interferon responses which can induce the overexpression of genes reported in SLE, and several variants within IRF8 could influence binding to the regulatory elements [4, 12]. Although very limited biological data of TMEM39A is published so far, its polymorphisms have been found to be associated with multiple sclerosis and SLE [4, 13‐15]. Additionally, several studies found genetic variants in orosomucoid like 3 (ORMDL3) and gasdermin B (GSDMB) were associated with the risk of autoimmune disease [16, 17]. On the basis of these studies, we hypothesized that certain novel variants in the loci described previously may contribute to the susceptibility to SLE.

In this study, we selected the six candidate genes, namely, IRF8, TMEM39A, IKZF3, ORMDL3, GSDMB, and ZPBP2, and screened for the putatively functional tagSNPs. We aimed to determine the association between the polymorphisms and susceptibility to SLE in a Chinese population.

In the screening stage, a few of tagSNPs for the six candidate genes were excluded from further analysis because they were found to have no polymorphic sites or to exhibited MAFs < 0.05 in Chinese Han Beijing population. Finally, 14 tagSNPs with predicted functional effects were selected for genotyping in a total of 885 subjects (Table 2). The details of the five identified genetic single-nucleotide variants in two genes, namely, TMEM39A rs2282175, rs4687859, rs12493175, rs13062955, and GSDMB rs9303281 were presented (Table 4). Additionally, there was no significant difference concerning the call rates between the SLE group and the control (p > 0.05). However, as shown in Table 5, the allelic distributions of rs4687859 and rs9303281 showed significant departure from the Hardy-Weinberg law for the controls. The allelic distributions of the three selected tag-SNPs, rs2282175, rs12493175, and rs13062955, of the TMEM39A gene met the Hardy-Weinberg principle (Table 5). Thus, we focused on the three selected tag-SNPs, rs2282175, rs12493175, and rs13062955, of the TMEM39A gene in the following analysis (Table 6).

The genotypic frequencies of rs12493175 and rs13062955 located in TMEM39A gene were significantly different between the SLE patients and the healthy controls. Compared with the common homozygous genotype, the CT and CT + TT genotypes in rs12493175 (p.adjust = 0.005, odds ratio (OR) 0.58, 95% CI 0.42 to 0.79; p.adjust = 0.007, OR 0.62, 95% CI 0.46 to 0.84, respectively) and the AC and AC + AA genotypes in rs13062955 (p.adjust = 0.002, OR 0.55, 95% CI 0.40 to 0.76; p.adjust = 0.007, OR 0.61, 95% CI 0.45 to 0.84, respectively) was observed to significantly reduce the risk of SLE. On the other hand, the difference in the frequency of rs2282175 was only marginal. The CT and CT + TT genotypes in rs2282175 was observed to modestly increase the risk of SLE (p.adjust = 0.054, OR 1.63, 95% CI 1.06 to 2.38; p.adjust = 0.054, OR 1.56, 95% CI 1.05 to 2.27, respectively). However, we did not find any other tagSNP associated with SLE risk in the genes of IRF8, IKZF3, ORMDL3, GSDMB and ZPBP2. We also evaluated the relation between the associated polymorphisms and the gene mRNA levels in peripheral blood mononuclear cells from 40 patients. Nevertheless, we failed to find any correlation between them (data not shown).

Haplotypes were constructed in both SLE and healthy controls and the haplotypes with frequency of > 3% were built from TMEM39A rs2282175, rs12493175 and rs13062955 (Table 7). The results show that the CGTA haplotype frequency was significantly low in the SLE patients (p = 0.019, OR 0.72, 95% CI 0.55 to 0.95). No difference was detected in the other haplotypes.

IRF8, TMEM39A and IKZF3-ZPBP2 were previously identified as susceptibility loci for SLE in the multiracial replication study [4], Besides, ORMDL3 and GSDMB were found to have susceptibility loci for autoimmune diseases [16, 17]. Thus we hypothesized certain novel associations in SNPs located in these genes could be identified in Chinese populations. To test this hypothesis, we selected 14 tagSNPs in these candidate genes to determine the association between the polymorphisms and SLE susceptibility in a Chinese Han population. Our findings showed that TMEM39A rs2282175, rs12493175, and rs13062955 were associated with SLE risk.

To date, almost no biological data of TMEM39A have been reported and only two SNPs in TMEM39A were identified as being associated with the susceptibility of autoimmune diseases. TMEM39A rs1132200 have been found to be associated with susceptibilities to multiple sclerosis and SLE in multiracial replication study [4, 13, 14]. but the recent studies showed that TMEM39A rs12494314, instead of rs1132200, was associated with SLE susceptibility in the Chinese population [15, 24]. In our current study, we identified three novel associations in SNPs located in TMEM39A as being associated with SLE susceptibility. The genotypic frequencies of rs12493175 and rs13062955 were significantly different between the SLE patients and the healthy controls, while the difference in the frequency of rs2282175 was only marginal. Among these polymorphisms, rs12493175 T-allele and rs13062955 A-allele were found to be associated with a reduced SLE risk, suggesting a protective factor to SLE. In contrast, rs2282175 T-allele was found to be associated with an increased SLE risk, suggesting a susceptibility factor to SLE. Haplotype analysis for TMEM39A SNPs revealed that the haplotype CGTA conferred a reduced risk of SLE. It is possible that the haplotype CGTA provides protection to SLE, resulting from the rs12493175 T and rs13062955 A alleles. It is worth noting that rs2282175 is located in the region of 5' upstream in TMEM39A and predicted to be a binding site of certain transcription factor. It is speculated that the C → T allele change at the rs2282175 site may influence the DNA binding ability of transcription factor c-Rel, which was predicted according to the different variants using the search tool of Alibaba 2.1 (http://​www.​gene-regulation.​com/​pub/​programs/​alibaba2). Although we did not find any relation between mRNA expression and the polymorphisms, it may be required to explore the possible biological significance of the SNPs in different cell subsets.

Several limitations in the current study should also be noted. First, due to the restricted number of study subjects and limited analysis capacity, we did not analyze the SNPs with rare MAF in the Chinese Han population, including those reported as risk loci for SLE in other ancestries, and mainly focused on the SNPs with predicted functional effect. Further research on the role of the rare variants should be carried out in a larger number of samples. As different populations have different genetic backgrounds, it is still necessary to perform the genetic analysis of multiracial study. Second, we still could not determine the causality of SLE-associated SNPs. For those variants in the large strong LD region, such as chromosome 17q21, it is difficult to determine which SNP is the true functional locus that contributes to SLE susceptibility independently. Better understanding whether the SNP is functionally relevant will require mechanistic and fine-mapping experiments. Third, our study did not assess the SNP-SNP interaction (epistasis). For the genetically complex disease, multiple interacting loci could contribute to SLE susceptibility. Additionally, as a heterogenetic disease, the contribution of genetic and environmental factors is very important for the disease [25]. Therefore, interaction between genetic and environmental factors is required to further clarify the pathogenesis of SLE.