- Research note
- Open Access
Contribution of SLC26A4 to the molecular diagnosis of nonsyndromic prelingual sensorineural hearing loss in a Brazilian cohort
BMC Research Notesvolume 11, Article number: 546 (2018)
Hereditary hearing loss (HL) is the most common sensorineural disorder in humans. Besides mutations in GJB2 and GJB6 genes, pathogenic variants in the SLC26A4 gene have been reported as a cause of hereditary HL due to its role in the physiology of the inner ear. In this research we wanted to investigate the prevalence of mutations in SLC26A4 in Brazilian patients with nonsyndromic prelingual sensorineural HL. We applied the high-resolution melting technique to screen 88 DNA samples from unrelated deaf individuals that were previously screened for GJB2, GJB6 and MT-RNR1 mutations.
The frequency of mutations in the SLC26A4 gene was 28.4%. Two novel mutations were found: p.Ile254Val and p.Asn382Lys. The mutation c.-66C>G (rs17154282) in the promoter region of SLC26A4, was the most frequent mutation found and was significantly associated with nonsyndromic prelingual sensorineural HL. After mutations in the GJB2, GJB6 and mitochondrial genes, SLC26A4 mutations are considered the next most common cause of hereditary HL in Brazilian as well as in other populations, which corroborates with our data. Furthermore, we suggest the inclusion of the SCL26A4 gene in the investigation of hereditary HL since there was an increase in the frequency of the mutations found, up to 22.7%.
Sensorineural hearing loss (SNHL) is the most common sensorineural impairment in humans, and it is associated with abnormalities of inner ear structures. In most cases, SNHL occurs before speech development (prelingual), and approximately 80% of these cases are affected by mutations in genes related to the hearing process [1, 2]. Many proteins have been associated with hereditary SNHL by affecting the hair-cell structure, extracellular matrix, ion homeostasis, and transcription factors [3, 4]. Mutations in two proteins encoded by the GJB2 and GJB6 genes (DFNB1 locus) expressed in cochlea cells, constitute the primary cause of genetic deafness, especially in Caucasian populations [5, 6]. However, studies with the Brazilian population have shown that the screening of the GJB2 and GJB6 genes explains the etiology of hearing loss (HL) in only 1–24.7% of the subjects analyzed, being the c.35delG (rs80338939) mutation in GJB2 (NM_004004.5) gene, the most frequent pathogenic variant [6,7,8,9]. Mutations in the SLC26A4 gene are associated with both syndromic (Pendred Syndrome) and nonsyndromic (DFNB4) cases of SNHL. This gene encodes pendrin, a transmembrane ion transporter which exchanges chloride for iodide and bicarbonate, in the thyroid gland and inner ear. In the cochlea, pendrin is expressed in the epithelial and supporting cells, and it is related to the regulation of pH homeostasis and the ion composition of the endolymph [10, 11]. After mutations in the GJB2 and GJB6 genes, mutations in SLC26A4 are considered the major cause of hereditary hearing loss in the Brazilian population and in many other populations [12,13,14,15], contributing to up to 14% of cases of moderate, profound or severe deafness . Thus, this study aimed to investigate and describe the prevalence of mutations in the SLC26A4 gene in nonsyndromic prelingual sensorineural hearing loss (SNHL) patients of a cohort from the Southeast of Brazil who had been previously tested for GJB2, GJB6, and MT-RNR1.
Patient samples and clinical data
This study was approved by the Ethics Research Committee of the University Hospital of the Ribeirão Preto Medical School-USP (n. 8736/2007). Genomic DNAs from 88 unrelated individuals diagnosed with nonsyndromic prelingual SNHL were extracted from whole blood samples, collected on EDTA, using Wizard® Genomic DNA Purification Kit (Promega®, Wisconsin, EUA), according to manufacturer’s instructions. To access clinical data, we reviewed the medical archives, and some variables were analyzed, such as type, degree, and progression of hearing loss, familial history, and risk factors. The study enrolled patients of both sexes at an age varying from 2–62 years old, who had been previously tested for GJB2 mutations by Sanger sequencing of the entire exon; for del(GJB6-D13S1830) and del(GJB6-D13S1854) deletions in GJB6 by multiplex PCR; as well as for m.1555A>G (rs267606617) and m.961delT point mutations in the mitochondrial gene MT-RNR1, by PCR and Restriction Fragment Length Polymorphism (PCR-FRLP) using HaeIII (Invitrogen®, Wisconsin, EUA) and MnlI (Fisher Scientific, New Hampshire, EUA) restriction enzymes.
We used DNA samples from 96 individuals of the same population as a control group. Individuals were all adults, of both sexes and did not present a personal history of hearing loss.
Screening of mutations on SLC26A4 gene
The genomic DNA of the affected individuals was examined for SLC26A4 mutations based on melting curve analyses compared with wild-type samples using High Resolution Melting (HRM) technique. A total of 26 HRM primers were adapted from Chen et al.  to cover all the 21 exons (including the non-coding Exon 1) of SLC26A4 with a maximum amplicon size of 250pb. The primers were optimized using In-Silico PCR (https://genome.ucsc.edu/cgi-bin/) and checked by the Melting Curve Prediction Software (https://www.dna.utah.edu/umelt/umelt.html) to reach the best melting curve profile (Table 1).
PCR for HRM analysis was performed on the 7500 Real-Time PCR Systems (Applied Biosystems®, California, EUA) using MeltDoctor™ HRM Master Mix (fluorescent DNA intercalating dye) (Applied Biosystems®, California, EUA). The reaction mixture in a final volume of 20 μL was made using 10 μL of 1X MeltDoctor™ HRM Master Mix, 2.4 μL of each primer (2.5 nM), 20 ng of genomic DNA and 1.2 μL of dH2O. The cycling and melting conditions were as follows: 40 cycles at 95 °C for 15 s, the annealing temperature of each amplicon for 1 min and one cycle at 95 °C for 10 s, 60 °C for 1 min, a melt at 95 °C for 15 s and 60 °C for 15 s. All samples were tested in duplicate.
Samples with mutations identified by HRM analysis were sequenced. Each sample with altered melting curves was purified using the Wizard SV Gel and PCR Clean-up System (Promega®, Wisconsin, EUA). Next, the product of purification was sequenced using Sanger sequencing on an automated 3500 XL Genetic Analyzer (Applied Biosystems®, California, EUA), using BigDye® Terminator v3.1 Cycle Sequencing Kit (Applied Biosystems®, California, EUA) according to the manufacturer´s instructions. Sequencing data were analyzed with the Geneious R7 software v7.1 using the NM_000441.1—GRCh37/hg19 sequence as reference.
In silico analysis of single nucleotide polymorphisms was done using three online tools (Sift Score, PolyPhen-2 and Combined Annotation Dependent Depletion—CADD) to predict the pathogenicity of the non-synonymous variants identified. Then, the software FunSeq and RegulomeDB were used to evaluate the effect of mutations on non-coding regions (exon 1). The Project HOPE Web Server tool was also used to predict the protein structural effects.
For association analyses, we used X2 Test and Fisher Exact Test, conducted using R Commander package version 2.4-x with R software environment. p-values lower than 0.05 were considered as a measurement of statistical significance.
In relation to the degree of hearing impairment, most individuals presented profound (55.7%) or severe (20.4%) hearing loss (HL). About 87.5% presented non-progressive HL, 28.4% reported a positive familial history of deafness and about 13.6% reported parental consanguinity. The frequency of mutations in the GJB2, GJB6, and mitochondrial genes, was 18.2%. The mutation c.35delG (rs80338939) in the GJB2 gene was the most frequent, being present in 14 individuals (15.9%) both in homozygous and heterozygous genotypes (Table 2). Three patients presented the del(GJB6-D13S1854) mutation in double heterozygosity with c.35delG in GJB2, and two patients presented the del(GJB6-D13S1854) in heterozygosity. No mutation was found in mitochondrial genes (Table 2). However, recessive genotypes and pathogenic mutations that can be associated with the phenotype were found in only 10.2% of the cases.
The inclusion of the SLC26A4 gene in the molecular screening showed a higher frequency of mutations. Ten non-synonymous mutations were identified in 25 individuals (28.4%). Two mutations were located in the promoter region (exon 1); seven were missense mutations, and two out of seven have not been described yet; as well as this, one synonymous mutation was found. About 22.7% of the mutations were found in heterozygosity or compound heterozygosity and 5.7% in double heterozygosity with the GJB2 and GJB6 genes (Table 3). For three of those mutations, it was possible to screen the frequency in the control group of 96 healthy individuals. The most frequent mutation found was the c.-66C>G (rs17154282), located in the non-coding exon 1 of the SLC26A4 gene (NM_000441.1) and it was found in 14.8% of the cohort. This mutation was significantly associated with nonsyndromic prelingual SNHL patients (OR = 0.33, 95% CI 0.09–1.05, p = 0.03684) when compared to the control group. The novel mutations p.Ile254Val and p.Asn382Lys were found, and this study constitutes the first report on both mutations in prelingual SNHL patients. Both mutations were shown to be pathogenic by the in silico tools PolyPhen-2 and CADD, but we found no significant association of those mutations with SNHL (p = 0.3052) when we compared to the mutation frequency in the control group. Three missense mutations also presented pathogenic scores with the in silico prediction tools (rs111033304; rs36039758 and rs55638457), but they had been previously reported as Benign/Likely benign by the ClinVar database (http://www.ncbi.nlm.nih.gov/clinvar/). No correlations were found between the clinical features and the genotypes.
The SLC26A4 (OMIM 605646) gene encodes pendrin, a protein associated with regulation of the ion composition and pH of endolymph in cochlear cells [11, 18]. Mutations in SLC26A4 gene may promote pendrin downregulation or loss of function, and constitute the second most frequent cause of autosomal recessive NSHL . In this study, the frequency of mutations in GJB2, GJB6, and mitochondrial genes was 18.2%, and the inclusion of the SLC26A4 in the investigation increased the frequency of mutations to up to 40.9%.
Hereditary NSHL is a disease characterized by an autosomal recessive inheritance pattern , however, about 18.1% of SLC26A4 mutations found in our study were monoallelic. These findings corroborate with many studies with NSHL patients [19,20,21] that report up to 61% of cases presenting heterozygous mutations in the SLC26A4 gene and suggest that these mutations might contribute to phenotype due to the presence of other mutations not detected (in genes or in regulatory regions not investigated), which together affect pendrin expression in the inner ear. The mutation c.-66C>G (rs17154282) was the most frequent mutation found in our study. It was present in 14.8% (13/88) of the individuals, mainly in a heterozygous genotype. This mutation was also reported by Choi et al.  in patients with NSHL and EVA. In the Tunisian population , a high frequency of c.-66C>G was also found in patients with autoimmune thyroid diseases, but this was considered as a non-pathogenic polymorphism. The c.-66C>G presents a high allele frequency specially in the African population [24, 25], which may explain the high frequency of that mutation in both the Tunisian and Brazilian populations, once both of whom present a strong African ancestry. In our study, the in silico analyses showed low pathogenicity scores (Table 3) but also suggested that the mutation affects a chromatin regulatory region that is also important for the ligation of enhancers and transcriptional factors (ELF1, RAD21, REST, ZEB1, CTCF). The screening of c.-66C>G in the control group of the same population revealed a significant association of that mutation with hereditary NSHL (OR = 0.33, 95% CI 0.09–1.05, p = 0.03684). Nevertheless, despite the lack of functional evidences, this mutation is reported as Benign/Likely benign on the ClinVar database, probably due to its high allele frequency. Even though there is conflicting data of pathogenicity, our data suggests that c.-66C>G may be related to hereditary NSHL. However, functional assays are necessary to validate the contribution of this mutation to the phenotype.
One case showed c.-66C>G in trans with c.-103T>C (rs60284988), which presents a nucleotide change in a conserved region. It was functionally demonstrated  that c.-103T>C integrates a critical binding site for transcriptional regulatory elements (as described by the prediction tools cited above), since c.-103T>C affects the binding of FOXI1, and it completely abolishes the FOXI1 activation of SLC26A4 transcription. Given this case, we suggest that the SLC26A4 5′UTR mutations contribute to the phenotype due to the recessive genotype.
Two novel mutations were found in this cohort, but only p.Asn382Lys presented pathogenic scores for all the three in silico prediction tools analyzed (Table 3). None of those mutations were found in the control group, and no significant association with the phenotype was found (p = 0.3052), probably due to the low number of individuals analyzed. The mutations p.Asn324Tyr (rs36039758) and p.Ile300Leu (rs111033304) also presented pathogenic scores but ClinVar also characterizes them as benign. In regard to p.Ile300Leu, this work constitutes the first report in hereditary NSHL [23, 27]. However, segregation analyses were done with a first degree NSHL relative for two of the three probands affected by p.Ile300Leu, and we suggest that this mutation is not related to the phenotype since no segregation of p.Ile300Leu within the NSHL was observed in those families. Segregation analyses were also possible for the p.Val609Gly (rs17154335) mutation, showing no segregation of that mutation within the investigated affected relatives. This corroborates with the results obtained by the prediction tools and many studies that have already characterized p.Val609Gly as a non-pathogenic mutation [19, 20, 28].
The NSHL is a multigenic complex disease involving many genetic and/or environmental factors . It is known that after mutations in the GJB2 and GJB6 genes, SLC26A4 is considered the next most common cause of hereditary HL in the Brazilian population and in many other populations [12,13,14,15]. Our data showed that the inclusion of a single gene in the investigation increased the frequency of mutations from 18.2 to 40.9%, reinforcing the importance of that gene to hereditary hearing loss genetic screening.
Many cases remained with an inconclusive molecular diagnosis, which demonstrates the need for more studies in order to characterize those mutations of unknown significance as well as other non-coding regions and novel genes associated with hereditary hearing loss.
neurosensory nonsyndromic recessive deafness 4
enlarged vestibular aqueduct
nonsyndromic hearing loss
polymerase chain reaction
sensorineural hearing loss
single nucleotide polymorphism
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SCSC, CHPG, CGPA, TOA, and GAM performed the clinical characterization, PCR standardization, HRM, Sanger sequencing and analyzed the data. VEFF and WASJ provided DNA samples and/or clinical/genetic data. SCS, GAM, VEFF, and WASJ wrote the manuscript. SCSC had full access to all the data in the study and took responsibility for the integrity of the data and the accuracy of the data analysis. All authors read and approved the final manuscript.
This work was possible due to the contribution of Prof. Dr. Wilson Araujo Silva Jr and the Regional Blood Center of Ribeirão Preto (FUNDHERP). We are also very thankful to all family members who participated in this study.
The authors declare that they have no competing interests.
Availability of data and materials
The publicly available datasets analyzed during the current study are available in the 1000 genomes (http://www.internationalgenome.org/) repository. The authors declare that all relevant data are included in the article and that it is also available from the corresponding author by request.
Consent for publication
Ethical approval and consent to participate
A written informed consent was obtained from all patients, and the ethical approval was granted by the Ethics Committee of the University Hospital of the Ribeirão Preto Medical School-USP (8736/2007).
This study was supported by the Molecular Genetics and Bioinformatics Laboratory, the Foundation for Education, Research and Assistance Support (FAEPA) of the University Hospital of the Ribeirão Preto Medical School—USP, and the National Council for Scientific and Technological Development (CNPq), which supported the Master’s scholarship of the first author (process number 141974/2015-0).
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