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BioMed Research International
Volume 2015, Article ID 318727, 8 pages
http://dx.doi.org/10.1155/2015/318727
Research Article

Single Nucleotide Polymorphisms of the GJB2 and GJB6 Genes Are Associated with Autosomal Recessive Nonsyndromic Hearing Loss

1Laboratory of Genetics and Molecular Biology, Graduate Program in Biomedical Sciences, Centro Universitário Hermínio Ometto (UNIARARAS), Avenida Maximiliano Barutto No. 500, Jardim Universitário, 13607339 Araras, SP, Brazil
2School of Biology, Centro Universitário Hermínio Ometto (UNIARARAS), 13607339 Araras, SP, Brazil
3School of Biomedicine, Centro Universitário Hermínio Ometto (UNIARARAS), 13607339 Araras, SP, Brazil
4Center of Molecular Biology and Genetic Engineering (CBMEG), Molecular Biology Laboratory, State University of Campinas (UNICAMP), 13083-970 Campinas, SP, Brazil

Received 7 October 2014; Accepted 1 March 2015

Academic Editor: Weidong Le

Copyright © 2015 Ana Paula Grillo et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Single nucleotide polymorphisms (SNPs) are important markers in many studies that link DNA sequence variations to phenotypic changes; such studies are expected to advance the understanding of human physiology and elucidate the molecular basis of diseases. The DFNB1 locus, which contains the GJB2 and GJB6 genes, plays a key role in nonsyndromic hearing loss. Previous studies have identified important mutations in this locus, but the contribution of SNPs in the genes has not yet been much investigated. The aim of this study was to investigate the association of nine polymorphisms located within the DFNB1 locus with the occurrence of autosomal recessive nonsyndromic hearing loss (ARNSHL). The SNPs rs3751385 (C/T), rs7994748 (C/T), rs7329857 (C/T), rs7987302 (G/A), rs7322538 (G/A), rs9315400 (C/T), rs877098 (C/T), rs945369 (A/C), and rs7333214 (T/G) were genotyped in 122 deaf patients and 132 healthy controls using allele-specific PCR. There were statistically significant differences between patients and controls, in terms of allelic frequencies in the SNPs rs3751385, rs7994748, rs7329857, rs7987302, rs945369, and rs7333214 (). No significant differences between the two groups were observed for rs7322538, rs9315400, and rs877098. Our results suggest that SNPs present in the GJB2 and GJB6 genes may have an influence on ARNSHL in humans.

1. Introduction

Hearing loss (HL) is a common congenital sensory disorder worldwide, affecting almost 600 million people. Approximately 2 to 6 children in 1,000 are affected by severe hearing loss at birth [1] or during early childhood. This is defined as prelingual deafness, with about half of cases attributable to genetic causes. Furthermore, many cases of late onset progressive HL also have a genetic origin, in addition to progressive HL associated with ageing [2]. According to the Hereditary Hearing Loss (HHL) homepage (http://hereditaryhearingloss.org/), over 140 loci for nonsyndromic HHL have been mapped, together with approximately 80 genes, and more than 1000 mutations have been identified in humans, making it one of the most genetically heterogeneous traits. However, in most cases, genetic hearing loss is a monogenic disorder. Biallelic mutations in 47 different genes have been reported for autosomal recessive nonsyndromic hearing loss (ARNSHL), which in many populations accounts for 80% of families with this type of deafness [3].

The occurrence of ARNSHL has been related to the DFNB1 locus (deafness, autosomal recessive 1) (OMIM 220290) at chromosome 13q11-q12, which contains two genes associated with hearing loss: GJB2 (gap junction protein, beta-2) (OMIM 121011) and GJB6 (gap junction protein, beta-6) (OMIM 604418), which codify the proteins encoding connexins 26 (Cx26) [4] and 30 (Cx30) [5], respectively. Mutations in these genes are the most frequent causes of ARNSHL in most populations worldwide, sometimes accounting for up to 50% of cases [6].

Direct intercellular communication is mainly mediated by gap junction channels, which in vertebrates are formed by members of the connexin protein family. Connexins are transmembrane proteins that regulate electrical signals and the passage between neighboring cells of ions, small biological molecules (<1000 Da) including sugars, nucleotides, and amino acids, secondary messengers such as Ca2+, cyclic AMP, and inositol triphosphate, and metabolic precursors [7]. Cochlear gap junctions, especially connexins Cx26 and Cx30, have been implicated in the maintenance of K+ homeostasis in the inner ear [8]. Cx26 and Cx30, the two most abundantly expressed gap junction proteins in the cochlea, are coexpressed as heteromeric connexons in nonsensory cells of the organ of Corti as well as in cells of the spiral ligament and stria vascularis [9]. Extensive genetic studies have been conducted to identify mutations in the DFNB1 locus; however, information is lacking concerning the potential association between nonsyndromic hearing loss and SNPs of the GJB2 and GJB6 genes [10].

Single nucleotide polymorphisms (SNPs) are the most abundant genetic markers at a specific location in the genome, occurring at a frequency of more than 1% in the human population [11]. The International HapMap Project has characterized over 3.1 million human SNPs, indicating a SNP density of approximately one per kilobase [12]. SNPs are of great interest in medical and pharmacological studies of disease susceptibility and drug response. They also provide powerful tools for a variety of medical genetic studies [13].

In view of all these observations, in an attempt to identify polymorphisms related to autosomal recessive nonsyndromic hearing loss, this study investigated the frequency of SNPs in the GJB2 and GJB6 genes by means of a case-control association study.

2. Materials and Methods

2.1. Ethics Statement

Written informed consent forms were obtained from all the participating subjects or from their parents. The study was approved by the Ethics Committee at Centro Universitário Hermínio Ometto de Araras (UNIARARAS), under protocol number 744/2010.

2.2. Study Subjects

The study involved 122 unrelated newborn patients of both genders (69 males and 53 females) with moderate to profound ARNSHL, together with 132 normal controls (CTL). The patients were from the Hearing and Language Stimulation Therapy Association, in Jundiaí (SP, Brazil). This institution is concerned with auditory and communication disorders, and since 2001 it has developed a universal hearing screening program. The majority of subjects studied were classified as Caucasian; however, many Brazilians have unique mixtures of Amerindian, European, and African ancestries in their genomic mosaic [14].

All patients underwent molecular analysis of the coding region and part of exon 1 and the flanking donor splicing site of GJB2 and the two deletions affecting the GJB6 gene (del(GJB6-D13S1830) and del(GJB6-D13S1854)). Also the 1555A>G, 827A>G, and 1494C>T mitochondrial mutations in the MTRNR1 gene and the 74555A>G mutation in the MTTS1 gene were analyzed. Following this screening, all individuals with an identified molecular cause for ARNSHL were excluded from the study. These previous analyses were performed at the Center of Molecular Biology and Genetic Engineering (CBMEG), Human Molecular Genetics Laboratory, State University of Campinas (UNICAMP), Campinas, SP, Brazil.

The normal controls were recruited from amongst the employees of UNIARARAS. In order to exclude the influence of inherited susceptibility factors, information about the control individuals was collected using questionnaires containing items concerning general health, medical conditions, and hereditary factors. Subjects with histories of head injury, otological disease, other diseases that could affect hearing, and previous or present treatment with ototoxic substances were excluded.

2.3. SNP Selection

Several SNPs covering the DFNB1 locus were analyzed, seven of these (rs3751385, rs7994748, rs7329857, rs7987302, rs877098, rs945369, and rs7333214) were selected from the HapMap database (available at http://www.hapmap.org/), and SNP genotyping data from the YRI population were downloaded into Haploview [15]. Only SNPs that passed quality control criteria (call rate ≥ 95%, minor allele frequency (MAF) ≥ 0.05, and Hardy-Weinberg disequilibrium ) were included in the genetic analysis. Two other SNPs (rs7322538 and rs9315400) were selected based on previous reports of association with deafness phenotypes [10]. Nine SNPs were analyzed, four in the GJB2 gene and five in the GJB6 gene. A summary of the selected SNPs is provided in Table 1.

Table 1: Summary of selected SNPs.
2.4. Genotyping

Genomic DNA was extracted from whole blood leukocytes using the standard phenol–chloroform method, as described previously [16]. For genotyping, all the DNA samples were normalized to a concentration of 50 ng/μL.

The SNP genotypes were determined by allele-specific PCR (AS-PCR) amplification. For analysis of allelic variants, two forward primers were designed, with the 3′ base of each primer matching only one of the biallelic SNP bases to be evaluated. Incorporation of a primer mismatch at the second or third base from the 3′ end of the primer has been shown to enhance the specificity of the PCR by further destabilizing the extension of the doubly mismatched primer [1719]. A common reverse primer (COM) was designed downstream of the polymorphic site. Control primers were also used for SNP coamplification of a portion of the human amelogenin (AMELX) gene [20]. These primers were therefore used as internal amplification controls. The sequences of the primers used in this study are listed in Table 2.

Table 2: Validation methods for each SNP analyzed.

Approximately 10% of samples, randomly selected, were regenotyped for cross-validation by restriction fragment length polymorphism PCR (RFLP-PCR) using restriction enzyme (New England Biolabs Inc., USA) (see Table 2) or by direct sequencing of PCR products using ABI BigDye Terminator, with analysis using an ABI PRISM 3700 DNA sequencer (Applied Biosystems, Foster City, USA). No inconsistencies were observed.

2.5. AS-PCR Amplification and Electrophoresis

The PCR procedures were performed using a 30 μL reaction volume containing 50 ng of template DNA, 0.5–0.7 pmol of each forward and reverse primer, 0.2 pmol of each control primer, 170 μM dNTP, an appropriate concentration of MgCl2 (Table 3), 0.01% (v/v) BSA, 1X reaction buffer (50 mM KCl, 20 mM Tris-HCl, pH 8.4), and 1 U Taq polymerase (Invitrogen, Itapevi, SP, Brazil). The samples were incubated at 95°C for 5 min, followed by 30 cycles of 1 min denaturation at 95°C, 1 min annealing (the times and annealing temperatures for different PCRs are described in Table 3), 1 min extension at 72°C, and a final extension at 72°C for 10 min. The amplicons (Table 3) were separated by electrophoresis in 1.5% agarose gel stained with ethidium bromide and were visualized and photographed using the Syngene G:BOX gel documentation system.

Table 3: AS-PCR primers and conditions.
2.6. Statistical Analysis

The Pearson goodness of fit test was used to assess deviation from Hardy-Weinberg equilibrium (HWE). Differences in genotype and allele frequencies between the study groups were compared by the chi-square test and/or Fisher’s exact test. Association between the SNPs and the risk of autosomal recessive nonsyndromic hearing loss was analyzed using the binary logistic regression test. Risk was expressed as odds ratio (OR) with 95% confidence intervals (CI). An was used as the cutoff for the baseline of risk-associated SNPs, and the baseline for risk-lowering SNPs was . The Bonferroni post hoc test was used to compare multiple groups, using the definition value (single tests) × number of tests. The minor allele frequency (MAF) for the study was calculated, and a test was performed to determine whether there was a significant difference between the MAF value obtained here and that in the public MAF database (NCBI dbSNP Build 132). All the statistical analyses were conducted using GraphPad Prism 5.0 software. A value < 0.05 was taken as statistically significant.

3. Results

A total of 254 individuals (132 in the control group and 122 in the patient group) were genotyped for 9 SNPs in the DFNB1 locus, using AS-PCR. Figure 1 shows a representative AS-PCR gel corresponding to the SNPs rs945369 and rs7333214. Significant deviations from Hardy-Weinberg equilibrium were detected in the genotype frequencies of both groups. HWE values for all the studied SNPs are summarized in Table 4. Analysis of the results indicated that the minor allele frequencies of the significant SNPs were in accordance with the information in the public database, although different frequencies were found for two of the SNPs, rs7994748 (MAF = 0.173) and rs7987302 (MAF = 0.026) (Table 5).

Table 4: Hardy-Weinberg proportions in the groups studied.
Table 5: Comparative analysis between minor allele frequency described in the database and minor allele frequency in the whole study group.
Figure 1: Electrophoretic patterns observed on AS-PCR analysis of the SNPs rs945369 (a) and rs7333214 (b). DNA ladder molecular weight marker (100 bp) was run in the first lane as labeled. The photo shows all three genotypes obtained from study individuals seen on the ethidium bromide-stained 1.5% agarose gel. AA: homozygote for the allele A; AC: heterozygote for the alleles A and C; CC: homozygote for the allele C (a). TT: homozygote for the allele T; TG: heterozygote for the alleles T and G; GG: homozygote for the allele G (b).

Out of the nine SNPs included in the study, six (66.7%) were found to be significantly associated with ARNSHL. Four of these (rs3751385, rs7994748, rs7329857, and rs7987302) were found in the GJB2 gene and two (rs945369 and rs7333214) in the GJB6 gene (Table 6). No significant associations were found for the other three SNPs (33.3%) genotyped. Three of the four significant SNPs of the GJB2 gene (rs3751385, rs7994748, and rs7329857) and one SNP of the GJB6 gene (rs7333214) remained statistically significant after application of the Bonferroni correction for multiple testing (×9, values of , 0.036, 3.478 × 10−4, and 0.0027, resp.). These four SNPs were therefore of sufficient interest to warrant further investigation. As revealed by the odds ratio (OR), four of the six SNPs were associated with a high risk of ARNSHL, with OR > 1, while the remaining two were associated with a decreased susceptibility to ARNSHL (). The rs7329857 SNP of the GJB2 gene was associated with the highest risk of ARNSHL, with OR of 11.70.

Table 6: Association analysis of selected SNPs in GJB2 and GJB6 genes with the ARNSHL.

Considering the risk-increasing SNPs, the rs3751385 (C/T) T allele (GJB2 gene) was identified in 90 out of 122 ARNSHL cases (74%), with 40 in heterozygous and 50 in homozygous genotypes. Likewise, the T allele of rs7994748 (C/T) was present in 92% of the cases (10 in heterozygous and 102 in homozygous genotypes). Other risk-associated SNPs in the GJB2 gene were only observed to occur in heterozygous genotypes, and these included 20 cases (16%) for rs7329857 (C/T) and 10 cases (8%) for rs7987302 (G/A). The presence of rs945369 (A/C) in the GJB6 gene was observed to be associated with decreased risk of ARNSHL, with 38 of the patients heterozygous (31%) and 23 of the cases (19%) CC homozygous. A genetic association of SNP rs7333214 (T/G) with ARNSHL was identified in 94% of the patients, with 61 heterozygous and 54 GG homozygous genotypes. The results of the association analysis are summarized in Table 6.

4. Discussion

Genome-wide association studies (GWAS) have successfully identified numerous loci that influence disease risk. Such techniques have been proved to offer powerful approaches for the screening of genes involved in complex diseases [21], including hearing loss, which occurs in around one per 1,000 newborns on average [22].

The current study evaluated the relationships between polymorphisms in the GJB2 and GJB6 genes and autosomal recessive nonsyndromic hearing loss in a sample of the Brazilian population. Evidence was found that SNPs in both genes were significantly associated with ARNSHL. Data for 122 patients and 132 controls indicated that GJB2 rs3751385 (C/T) was associated with hearing loss susceptibility, in agreement with previously published research [21, 23, 24].

The T allele of this SNP (rs3751385) has also been shown to be a risk factor associated with chronic plaque psoriasis in Chinese Han population patients [25]. A similar finding was reported for Chinese patients with psoriatic arthritis [26], possibly because connexin 26 (Cx26) has been found to be highly expressed in psoriasis plaques. Cx26 is widely expressed in most human tissues, including the ectoderm-derived epithelia of the cochlea, cornea, and skin [27].

Wilch et al. [28] previously showed that the expression of GJB2 and GJB6 diminished in the presence of the rs7333214 G allele. Conversely, in this study, the presence of the T allele was found to be positively associated with ARNSHL.

Here, to the best of our knowledge, we describe for the first time the association between the rs7994748, rs7329857, rs7987302, and rs945369 SNPs and ARNSHL. The results indicate that these genetic changes may be important determinants of hearing impairment risk in the studied population. The rs7994748 and rs945369 SNPs are present in the intronic regions of the GJB2 and GJB6 genes, respectively. It has been shown previously that SNPs present in the noncoding region can modulate gene expression [29]. The rs3751385 and rs7329857 SNPs are located in the 3′UTR region of the GJB2 gene, while rs7333214 is found in the GJB6 gene. The 3′UTR region of a gene is usually important for regulation of processes such as transcript cleavage, alternative polyadenylation, and mRNA nuclear export [30]. Mutations in 3′UTR of certain genes have been reported to be associated with several genetic diseases [3133]. Recently, Ramsebner et al. [34] showed that the rs117685390 C allele in the regulatory region of the human GJB2 gene could contribute to autosomal recessive nonsyndromic hearing loss.

Our study showed no significant differences between control and hearing loss subjects in terms of the distribution of alleles of the rs7322538, rs9315400, and rs877098 SNPs in the GJB6 gene. Similarly, no significant differences were detected between noise-induced hearing loss (NIHL) and normal groups when Abreu-Silva and colleagues [35] compared allele and genotype frequencies for the rs877098 SNP. Elsewhere, negative associations of rs7322538 with sporadic hearing impairment were found in the Chinese population [10]. The same study showed a significant difference in allele frequency for rs9315400, most likely due to the different ethnicity.

5. Conclusions

The present findings indicate that the rs7322538, rs9315400, and rs877098 SNPs in the GJB6 gene are not a significant risk factor for the development of ARNSHL in the Brazilian population. However, in contrast to these SNPs, it was found that carriers of the T allele of the SNPs rs3751385 (C/T), rs7994748 (C/T), rs7329857 (C/T), and rs7333214 (T/G) are at increased risk of ARNSHL.

Further studies are required to confirm these findings and to explore the hypothesis that the rs7994748 T, rs7329857 T, rs7987302 A, and rs945369 A alleles could be used as biomarkers for the development of autosomal recessive nonsyndromic hearing loss in Brazilian populations and could be included in assessments of the risk of developing ARNSHL. Finally, we provide important evidence of the association of SNPs in the GJB2 and GJB6 genes with hearing loss. The findings of this study contribute to an understanding of the intricate associations and gene interactions involved in hereditary hearing loss.

Conflict of Interests

The authors declare that there is no conflict of interests.

Authors’ Contribution

Camila Andréa de Oliveira conceived and designed the experiments. Ana Paula Grillo, Flávia Marcorin de Oliveira, Gabriela Queila de Carvalho, Ruan Felipe Vieira Medrano, and Sueli Matilde da Silva-Costa performed the experiments. Camila Andréa de Oliveira analyzed the data. Ana Paula Grillo, Flávia Marcorin de Oliveira, Gabriela Queila de Carvalho, and Edi Lúcia Sartorato contributed reagents, materials, and analysis tools. Camila Andréa de Oliveira wrote the paper.

Acknowledgments

The authors sincerely thank all the subjects who participated in the study and Fundação Hermínio Ometto/FHO and PIBIC/CNPq for their support.

References

  1. C. C. Morton and W. E. Nance, “Newborn hearing screening—a silent revolution,” The New England Journal of Medicine, vol. 354, no. 20, pp. 2151–2164, 2006. View at Publisher · View at Google Scholar · View at Scopus
  2. R. Birkenhäger, N. Lüblinghoff, E. Prera, C. Schild, A. Aschendorff, and S. Arndt, “Autosomal dominant prelingual hearing loss with palmoplantar keratoderma syndrome: variability in clinical expression from mutations of R75W and R75Q in the GJB2 gene,” The American Journal of Medical Genetics Part A, vol. 152, no. 7, pp. 1798–1802, 2010. View at Publisher · View at Google Scholar · View at Scopus
  3. N. Hilgert, R. J. H. Smith, and G. van Camp, “Forty-six genes causing nonsyndromic hearing impairment: which ones should be analyzed in DNA diagnostics?” Mutation Research—Reviews in Mutation Research, vol. 681, no. 2-3, pp. 189–196, 2009. View at Publisher · View at Google Scholar · View at Scopus
  4. D. P. Kelsell, J. Dunlop, H. P. Stevens et al., “Connexin 26 mutations in hereditary non-syndromic sensorineural deafness,” Nature, vol. 387, no. 6628, pp. 80–83, 1997. View at Publisher · View at Google Scholar · View at Scopus
  5. I. del Castillo, M. Villamar, M. A. Moreno-Pelayo et al., “A deletion involving the connexin 30 gene in nonsyndromic hearing impairment,” The New England Journal of Medicine, vol. 346, no. 4, pp. 243–249, 2002. View at Publisher · View at Google Scholar · View at Scopus
  6. A. Kenneson, K. V. N. Braun, and C. Boyle, “GJB2 (connexin 26) variants and nonsyndromic sensorineural hearing loss: a HuGE review,” Genetics in Medicine, vol. 4, no. 4, pp. 258–274, 2002. View at Publisher · View at Google Scholar · View at Scopus
  7. S. Maeda and T. Tsukihara, “Structure of the gap junction channel and its implications for its biological functions,” Cellular and Molecular Life Sciences, vol. 68, no. 7, pp. 1115–1129, 2011. View at Publisher · View at Google Scholar · View at Scopus
  8. T. Kikuchi, R. S. Kimura, D. L. Paul, T. Takasaka, and J. C. Adams, “Gap junction systems in the mammalian cochlea,” Brain Research Reviews, vol. 32, no. 1, pp. 163–166, 2000. View at Publisher · View at Google Scholar · View at Scopus
  9. J. Sun, S. Ahmad, S. Chen et al., “Cochlear gap junctions coassembled from Cx26 and 30 show faster intercellular Ca2+ signaling than homomeric counterparts,” The American Journal of Physiology - Cell Physiology, vol. 288, no. 3, pp. C613–C623, 2005. View at Publisher · View at Google Scholar · View at Scopus
  10. H.-B. Cheng, Z.-B. Chen, Q.-J. Wei, Y.-J. Lu, G.-Q. Xing, and X. Cao, “Single nucleotide polymorphisms and haplotypes analysis of DFNB1 locus in Chinese sporadic hearing impairment population,” Chinese Medical Journal, vol. 122, no. 13, pp. 1549–1553, 2009. View at Publisher · View at Google Scholar · View at Scopus
  11. D. G. Wang, J.-B. Fan, C.-J. Siao et al., “Large-scale identification, mapping, and genotyping of single- nucleotide polymorphisms in the human genome,” Science, vol. 280, no. 5366, pp. 1077–1082, 1998. View at Publisher · View at Google Scholar · View at Scopus
  12. The International HapMap Consortium, “A second generation human haplotype map of over 3.1 million SNPs,” Nature, vol. 449, no. 7164, pp. 851–861, 2007. View at Google Scholar
  13. N. Noda, H. Tani, N. Morita et al., “Estimation of single-nucleotide polymorphism allele frequency by alternately binding probe competitive polymerase chain reaction,” Analytica Chimica Acta, vol. 608, no. 2, pp. 211–216, 2008. View at Publisher · View at Google Scholar · View at Scopus
  14. S. D. J. Pena, L. Bastos-Rodrigues, J. R. Pimenta, and S. P. Bydlowski, “DNA tests probe the genomic ancestry of Brazilians,” Brazilian Journal of Medical and Biological Research, vol. 42, no. 10, pp. 870–876, 2009. View at Publisher · View at Google Scholar · View at Scopus
  15. J. C. Barrett, B. Fry, J. Maller, and M. J. Daly, “Haploview: analysis and visualization of LD and haplotype maps,” Bioinformatics, vol. 21, no. 2, pp. 263–265, 2005. View at Publisher · View at Google Scholar · View at Scopus
  16. J. Sambrook, E. F. Fritsch, and T. Maniatis, Molecular Cloning: A Laboratory Manual, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY, USA, 2nd edition, 1989.
  17. S. Little, “Unit. 9.8.1 amplification-refractory mutation system (ARMS) analysis of point mutations,” in Current Protocols in Human Genetics, chapter 7, 2001. View at Publisher · View at Google Scholar
  18. C. R. Newton, A. Graham, L. E. Heptinstall et al., “Analysis of any point mutation in DNA. The aplivication refractory mutation system (ARMS),” Nucleic Acids Research, vol. 17, no. 7, pp. 2503–2516, 1989. View at Publisher · View at Google Scholar · View at Scopus
  19. R. Okimoto and J. B. Dodgson, “Improved PCR amplification of multiple specific alleles (PAMSA) using internally mismatched primers,” BioTechniques, vol. 21, no. 1, pp. 20–26, 1996. View at Google Scholar · View at Scopus
  20. T. Antoniadi, R. Rabionet, C. Kroupis et al., “High prevalence in the Greek population of the 35delG mutation in the connexin 26 gene causing prelingual deafness,” Clinical Genetics, vol. 55, no. 5, pp. 381–382, 1999. View at Google Scholar · View at Scopus
  21. S. P. Dickson, K. Wang, I. Krantz, H. Hakonarson, and D. B. Goldstein, “Rare variants create synthetic genome-wide associations,” PLoS Biology, vol. 8, no. 1, Article ID e1000294, 2010. View at Publisher · View at Google Scholar · View at Scopus
  22. M. Tekin, K. S. Arnos, and A. Pandya, “Advances in hereditary deafness,” The Lancet, vol. 358, no. 9287, pp. 1082–1090, 2001. View at Publisher · View at Google Scholar · View at Scopus
  23. G. Minarik, E. Ferakova, A. Ficek, H. Polakova, and L. Kadasi, “GJB2 gene mutations in Slovak hearing-impaired patients of Caucasian origin: spectrum, frequencies and SNP analysis,” Clinical Genetics, vol. 68, no. 6, pp. 554–557, 2005. View at Publisher · View at Google Scholar · View at Scopus
  24. L. van Laer, P.-I. Carlsson, N. Ottschytsch et al., “The contribution of genes involved in potassium-recycling in the inner ear to noise-induced hearing loss,” Human Mutation, vol. 27, no. 8, pp. 786–795, 2006. View at Publisher · View at Google Scholar · View at Scopus
  25. Q.-P. Liu, L.-S. Wu, F.-F. Li et al., “The association between GJB2 gene polymorphism and psoriasis: a verification study,” Archives of Dermatological Research, vol. 304, no. 9, pp. 769–772, 2012. View at Publisher · View at Google Scholar · View at Scopus
  26. Q. Yang, H. Liu, L. Qu et al., “Investigation of 20 non-HLA (human leucocyte antigen) psoriasis susceptibility loci in Chinese patients with psoriatic arthritis and psoriasis vulgaris,” British Journal of Dermatology, vol. 168, no. 5, pp. 1060–1065, 2013. View at Publisher · View at Google Scholar · View at Scopus
  27. D. Salomon, E. Masgrau, S. Vischer et al., “Topography in mammalian connexins in human skin,” Journal of Investigative Dermatology, vol. 103, no. 2, pp. 240–247, 1994. View at Publisher · View at Google Scholar · View at Scopus
  28. E. Wilch, M. Zhu, K. B. Burkhart et al., “Expression of GJB2 and GJB6 is reduced in a novel DFNB1 allele,” The American Journal of Human Genetics, vol. 79, no. 1, pp. 174–179, 2006. View at Publisher · View at Google Scholar · View at Scopus
  29. G.-J. Wang, P. Yang, and H.-G. Xie, “Gene variants in noncoding regions and their possible consequences,” Pharmacogenomics, vol. 7, no. 2, pp. 203–209, 2006. View at Publisher · View at Google Scholar · View at Scopus
  30. E. A. Grzybowska, A. Wilczynska, and J. A. Siedlecki, “Breakthroughs and views: regulatory functions of 3′UTRs,” Biochemical and Biophysical Research Communications, vol. 288, no. 2, pp. 291–295, 2001. View at Publisher · View at Google Scholar · View at Scopus
  31. B. Conne, A. Stutz, and J.-D. Vassalli, “The 3′ untranslated region of messenger RNA: a molecular ‘hotspot’ for pathology?” Nature Medicine, vol. 6, no. 6, pp. 637–641, 2000. View at Publisher · View at Google Scholar · View at Scopus
  32. B. Mazumder, V. Seshadri, and P. L. Fox, “Translational control by the 3-UTR: the ends specify the means,” Trends in Biochemical Sciences, vol. 28, no. 2, pp. 91–98, 2003. View at Publisher · View at Google Scholar · View at Scopus
  33. J. T. Mendell and H. C. Dietz, “When the message goes awry: disease-producing mutations that influence mRNA content and performance,” Cell, vol. 107, no. 4, pp. 411–414, 2001. View at Publisher · View at Google Scholar · View at Scopus
  34. R. Ramsebner, M. Ludwig, T. Lucas et al., “Identification of a SNP in a regulatory region of GJB2 associated with idiopathic nonsyndromic autosomal recessive hearing loss in a multicenter study,” Otology & Neurotology, vol. 34, no. 4, pp. 650–656, 2013. View at Publisher · View at Google Scholar · View at Scopus
  35. R. S. Abreu-Silva, D. Rincon, A. R. V. R. Horimoto et al., “The search of a genetic basis for noise-induced hearing loss (NIHL),” Annals of Human Biology, vol. 38, no. 2, pp. 210–218, 2011. View at Publisher · View at Google Scholar · View at Scopus
  36. S. T. Sherry, M.-H. Ward, M. Kholodov et al., “DbSNP: the NCBI database of genetic variation,” Nucleic Acids Research, vol. 29, no. 1, pp. 308–311, 2001. View at Publisher · View at Google Scholar · View at Scopus