Mutation Analysis of the Common Deafness Genes in Patients with Nonsyndromic Hearing Loss in Linyi by SNPscan Assay

Zhang, Fengguo; Xiao, Yun; Xu, Lei; Zhang, Xue; Zhang, Guodong; Li, Jianfeng; Lv, Huaiqing; Bai, Xiaohui; Wang, Haibo

doi:https://doi.org/10.1155/2016/1302914

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Advances in Molecular Genetics and the Molecular Biology of Deafness

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Volume 2016 | Article ID 1302914 | https://doi.org/10.1155/2016/1302914

Mutation Analysis of the Common Deafness Genes in Patients with Nonsyndromic Hearing Loss in Linyi by SNPscan Assay

Fengguo Zhang,^1,2Yun Xiao,^1,2Lei Xu,^1,2Xue Zhang,^1,2Guodong Zhang,^1,2Jianfeng Li,^1,2Huaiqing Lv,³Xiaohui Bai,^1,2and Haibo Wang^1,2

Academic Editor: Hideaki Moteki

Received15 Jan 2016

Revised06 Apr 2016

Accepted17 Apr 2016

Published09 May 2016

Abstract

Hearing loss is a common sensory disorder, and at least 50% of cases are due to a genetic etiology. Although hundreds of genes have been reported to be associated with nonsyndromic hearing loss, GJB2, SLC26A4, and mtDNA12SrRNA are the major contributors. However, the mutation spectrum of these common deafness genes varies among different ethnic groups. The present work summarized mutations in these three genes and their prevalence in 339 patients with nonsyndromic hearing loss at three different special education schools and one children’s hospital in Linyi, China. A new multiplex genetic screening system “SNPscan assay” was employed to detect a total of 115 mutations of the above three genes. Finally, 48.67% of the patients were identified with hereditary hearing loss caused by mutations in GJB2, SLC26A4, and mtDNA12SrRNA. The carrying rate of mutations in the three genes was 37.76%, 19.75%, and 4.72%, respectively. This mutation profile in our study is distinct from other parts of China, with high mutation rate of GJB2 suggesting a unique mutation spectrum in this area.

1. Introduction

Hearing loss or deafness is one of the most common neurosensory disorders in humans affecting about 1 to 3 in 1000 children worldwide [1]. It has been estimated that 30,000 newborns are detected with congenital hearing loss per 20 million live births every year in China [2], and approximately 50% of hearing loss is caused by a genetic etiology. At least 70% of all cases are classified as nonsyndromic hearing loss (NSHL) manifesting with isolated hearing loss without other associated clinical features. Of all NSHL, 75%–80% are autosomal recessive hereditary hearing loss, 15%–20% are autosomal dominant, 5% are X-linked, and 1% are inherited by mitochondrial genes [3].

Many previous genetic screening studies have shown that a large proportion of NSHL is caused by the mutations of a few genes, such as gap junction beta-2 protein (GJB2), solute carrier family 26 member 4 (SLC26A4), and mitochondrial DNA (mtDNA) 12SrRNA [4, 5]. Therefore, mutation screening of these common deafness-causing genes is of vital importance during genetic testing and counseling of deafness.

China harboring the highest population in the world is consisting of 56 nationalities. The mutation spectrum of the common deafness genes may vary among different ethnic nationalities due to geographical and language separation. The city Linyi with the biggest population and the largest area in Shandong Province locates in the east part of China. Almost all the populations in this area are Han nationality. People in Linyi are always impressed by introversion and rusticity. Because of its desolate geographical condition, Linyi city is a relatively conservative area with a less migration of population and an obstructive communication with other regions. Also, it has a less-developed economics for a long time. But to our knowledge, no systematic mutation analysis of deaf patients in Linyi has been reported previously. Therefore, there is a reason to believe that mutation spectrum of common deafness genes in patients with NSHL in this area must have a unique and special characteristic.

Up to now, many screening methods are used to detect the mutations of hearing loss, for example, direct sequencing, microarray, and PCR-restriction fragment length polymorphism (PCR-RFLP). These methods are either too expensive or time-consuming. Du et al. established a universal genetic screening system of hearing loss called the SNPscan assay which could detect 115 mutations of GJB2, SLC26A4, and mtDNA12SrRNA genes [6]. These selected mutations accounted for up to 90% of hearing loss caused by the most common deafness-causing genes in Chinese population.

In this study, we performed a comprehensive analysis of 3 common deafness-causing genes, GJB2, SLC26A4, and mtDNA12SrRNA, by SNPscan assay in 339 patients with NSHL from Linyi in eastern China. The aim was to investigate the molecular etiology in order to provide effective genetic counseling for hearing loss patients in this area.

2. Materials and Methods

2.1. Recruitment of the Subjects

A total of 339 subjects with NSHL from unrelated families were included in this study. They came from three different special education schools and one children’s hospital in Linyi. Clinical questionnaire and informed consent were obtained from all subjects or their parents on their behalf. Clinical questionnaire showed basic information, including name, age, family history, health condition of the mother during pregnancy, and a clinical record of the patient, such as infections, possible head or brain injury, and the use of aminoglycoside antibiotics [7]. Physical and neurological examination was performed with special attention to renal, electrocardiac, and ophthalmologic differences to exclude those with syndromic hearing loss. An audiologic evaluation was performed including otoscope examination, tympanometry, and pure-tone audiometry (PTA). Auditory brainstem response (ABR) was employed in subjects when they were too young to accomplish the PTA test, and temporal bone computed tomography (CT) scan was also performed on participants for diagnosis of enlarged vestibular aqueduct (EVA) or inner ear malformation.

The onset of hearing impairment was categorized as prelingual/early (≤6 years) and late (>6 years). The degree of hearing impairment was calculated on the average of PTA in the speech frequencies 0.25, 0.5, 1, 2, and 4 kHz. Normal hearing was classified as PTA ≤ 25 dB nHL, mild hearing loss as PTA > 25 dB nHL and ≤40 dB nHL, moderate hearing loss as PTA > 40 dB nHL and ≤60 dB nHL, severe hearing loss as PTA > 60 dB nHL and ≤80 dB nHL, and profound hearing loss as PTA > 80 dB nHL. To enroll in this study, all subjects should have bilateral, permanent sensorineural hearing impairment. This study was approved by the Ethics Committee of Shandong Provincial Hospital.

2.2. DNA Samples

Genomic DNA for all 339 patients was prepared from 2 mL of peripheral blood with AxyPrep Genomic Blood DNA Extraction Kit (AXYGEN, USA). For the evaluation of the quantity and quality of extracted DNA, spectrophotometry (UNICO 2100, USA) and 1% agarose gel electrophoresis were carried out according to routine methods [8].

2.3. SNPscan for Mutation Detection

Two customized multiplex SNPscan assays from Genesky Biotechnologies Inc. (Shanghai, China) were designed to capture a total of 115 mutations of the three common deafness-causing genes as previously described (Table S1 in Supplementary Material available online at http://dx.doi.org/10.1155/2016/1302914): one is 53-plex and the other is 62-plex [6]. As a high-throughput and cost-saving SNP genotyping method, the SNPscan assay is based on double ligation and multiplex fluorescence PCR as described [9–11]. The SNPscan assays were done according to the detailed protocol described by Du et al. [6].

2.4. Statistical Analysis

The statistical analysis was performed using SAS 9.1.3 software (SAS, USA).

3. Result

3.1. Characterization of the Deaf Probands

A total of 339 probands with NSHL were recruited in this sequencing study, including 304 simplex and 35 multiplex probands. Simplex probands refer to the sporadic patients whose families have no one else suffering from hearing loss. Multiplex probands mean that there is at least one first- or second-degree deaf relative in the family. Clinical characterization of the deaf probands was summarized in Table 1. The patient cohort consisted of 196 males and 143 females, and they were all Han Chinese. The ages of the probands varied between a few months and 24 years (mean 8.9 years, 95% CI 8.3–9.5 years). Only one proband had late-onset, progressive, and moderate sensorineural hearing loss. All other probands had prelingual or early-onset sensorineural hearing loss. Hearing tests demonstrated that the level of hearing loss was severe to profound in 328 patients. The remaining 11 patients showed moderate hearing loss.

Among all these patients, 48.67% were identified with hereditary hearing loss by means of the SNPscan assay (Figure 1). There were 104 patients (30.68%) affected by GJB2 mutations: 49 homozygotes and 55 compound heterozygotes. 45 (13.27%) patients carried two SLC26A4 pathogenic mutations: fourteen homozygotes and 31 compound heterozygotes. 16 (4.72%) patients harbored mtDNA12SrRNA mutations consisting of 15 homoplasmic mutations and 1 heteroplasmic mutation.

3.2. Mutations in GJB2 Gene

Eleven variants were identified in this cohort. They were three frameshift deletions (c.176_191del16, c.235delC, and c.299_300delAT), two frameshift insertions (c.34_35insG and c.511_512insAACG), four missense mutations [c.109G>A (p.V37I), c.257C>G (p.T86R), c.427C>T (p.R143W), and c.571T>C (p.F191L)], one nonsense mutation c.9G>A (p.W3X), and one splicing site mutation IVS1+1G>A (shown in Table 2). Nine of them were pathological mutations which have been determined previously. The category of two nucleotide changes was unknown (c.9G>A, c.571T>C). The mutant alleles of GJB2 accounted for 34.37% (233/678) of the total alleles in all patients (Table 3). The most common mutation allele of GJB2 in this area was c.235delC with a mutant frequency of 20.65% (140/678). The second common was c.299_300delAT of 5.60% (38/678), followed by c.109G>A of 2.51% (17/678), c.34_35insG of 1.77% (12/678), c.176_191del16 of 1.33% (9/678), c.511_512insAACG of 1.18% (8/678), c.257C>G of 0.29% (2/678), c.427C>T of 0.29% (2/678), and IVS1+1G>A of 0.15% (1/678) (1/678) (Table 3).

A total of 104 patients (30.68%) were confirmed to be associated with hereditary hearing loss caused by GJB2 mutation: 49 homozygotes (42 with the c.235delC allele, 4 with c.299_300delAT, and 3 with the c.109G>A allele) and 55 compound heterozygotes. Twenty patients (5.90%) had monoallelic variants in the heterozygous form: ten with c.235delC, eight with c.109G>A, one with c.299_300delAT, and one with c.511_512insAACG. Totally, 128 (37.76%, 128/339) patients had molecular defects in GJB2 gene including three patients with c.571T>C mutation (Table 2).

The most common mutation allele of GJB2 was c.235delC with a mutant frequency of 20.65% (140/678) affecting 98 patients. Among these patients carrying at least one c.235delC allele, there were 42 homozygotes, 46 compound heterozygotes, and 10 single heterozygotes.

3.3. Mutations in SLC26A4 Gene

Nineteen variants were identified in this cohort, including 12 missense mutations [c.147C>G (p.S49R), c.269C>T (p.S90L), c.563T>C (p.I188T), c.589G>A (p.G197R), c.1173C>A (p.S391R), c.1174A>T (p.N392Y), c.1225C>T (p.R409C), c.1226G>A (p.R409H), c.1975G>C (p.V659L), c.1985G>A (p.C662Y), c.2027T>A (p.L676Q), and c.2168A>G (p.H723R)], four nonsense mutations [c.235C>T (p.R79X), c.946G>T (p.G316X), c.1318A>T (p.K440X), and c.1540C>T (p.Q514X)], two splicing site mutations (c.919-2A>G, c.1707+5 G>A), and one frameshift insertion mutation (c.1547_1548insC) (Table 5). Combining the prediction of SIFT and Polyphen-2 with the results of previous studies, all variants analyzed in our cohort were considered pathogenic mutations except c.147C>G (p.S49R) for an unknown significant pathogenicity (Table 4).

There were 45 (13.27%) patients who were confirmed to have inherited hearing loss because they carried two SLC26A4 pathogenic mutations: fourteen homozygotes (13 c. IVS 7-2A>G and 1 c.2168A>G) and 31 compound heterozygotes. And 22 (6.49%) patients who were identified carried one SLC26A4 pathogenic mutation. Thus, the detection rate of SLC26A4 mutations was 19.76% (67/339) in this patient cohort. All patients carrying two mutations were diagnosed with EVA syndrome by CT scan of the temporal bone. And 17 out of 22 patients carrying one pathogenic mutation were diagnosed with EVA syndrome.

The most common mutation allele of SLC26A4 was c.919-2A>G with a mutant frequency of 9.59% (65/678) affecting 52 patients. Among these patients carrying at least one c.919-2A>G mutation allele, there were 13 homozygotes, 27 compound heterozygotes, and 12 single heterozygotes. The second common mutation allele of SLC26A4 was c.2168A>G with a mutant frequency of 2.21% (15/678).

3.4. Mutations in mtDNA12SrRNA

Sixteen patients (4.72%) carried an mtDNA12SrRNA mutation, where all of which were the m.1555A>G mutation containing 15 homoplasmic mutations and 1 heteroplasmic mutations. Ten of these patients had a clear history of aminoglycoside antibiotic use.

4. Discussion

Currently, many studies have reported that GJB2, SLC26A4, and mtDNA12SrRNA genes are the most common causes in Chinese NSHL population [12–14]. In the present study we have screened for the common deafness gene mutations of 339 NSHL children from Linyi, east part of China. SNPscan assay was used to perform genotyping detection of these three common deafness-causing genes. Compared with other methods, this technique is accurate, rapid, and economically effective. As the novel mutations have been reported successively, more mutation alleles should be added in the SNPscan assay.

4.1. GJB2 Mutation Analysis

In this present study, GJB2 mutations were detected in 37.76% (128/339) of all patients, including 30.68% (104/339) with two pathogenic mutations and 7.08% (24/339) with only one mutant allele. The c.235delC and c.299_300delAT were the most frequent mutations in the NSHL patients in Linyi, whereas the hotspot mutation in Xiamen, China, was c.109G>A [7].

The frameshift mutation c.235delC has been reported as the most common mutation causing premature protein termination in hearing impaired patients in East and Southeast Asia, while lower frequencies were reported in Europe and Oceania [15–24]. The c.235delC mutation allele frequency was 20.65% (140/678) in this work. In an earlier nationwide study, Dai et al. analyzed the GJB2 mutation of 2063 unrelated NSHL students from 23 different regions of China, and the c.235delC mutation allele frequency was 12.34% (509/4,126) [25]. Compared with 12.34% in his study, the difference in the c.235delC mutation allele frequency was significant (), reflecting a certain distinction of the c.235delC mutation frequency in Linyi and other areas. There was a higher carrying rate of c.235delC in the Linyi deaf population.

4.2. SLC26A4 Mutation Analysis

According to previous study, more than 200 mutations have been described in the SLC26A4 gene with Pendred syndrome (PS) and enlarged vestibular aqueduct (EVA) syndrome (http://www.healthcare.uiowa.edu/labs/pendredandbor/) showing specific distinctions among racial backgrounds. Most of them are missense mutations, in addition to frameshift mutations, splice site mutations, insertions, or deletions [26].

The mutation hotspots of SLC26A4 differed among different nations and areas. In the present study, the most common mutation in our patient cohort was c.IVS7-2A>G and the mutation allele frequency was 9.59% (65/678), whereas the mutation hot spots are p.T416P and c.IVS8+1G>A [27] in Northern Europe, p.H723R and c. IVS7-2A>G in South Korea [15], and p.H723R in Japan [28]. It was reported in a mutation study of a large cohort in Chinese deaf population that the most common SLC26A4 mutation was also IVS7-2A>G (8.65%, 566/6,542) [12]. Although the mutation allele frequency was a little higher (9.59%) in our study, these frequencies of c.IVS7-2A>G are not significantly different ( = 0.41).

4.3. mtDNA12SrRNA Mutation Analysis

Patients with mutations in mtDNA12SrRNA can be affected with aminoglycoside antibiotic-induced deafness showing a hereditary model of maternal inheritance. And m.1494C>T and m.1555A>G are the most common mutations of this mitochondrial gene. Mutate rate of this gene varies among racial and geographic origins in populations with NSHL, with a frequency of 0.6–2.5% in Caucasians [29–32], 1.8% in Turks [30], 0.7% in Germans, 1.8% in Hungarians, and 2.4% in Poles [29]. In our study, we found that 4.72% of the patients were identified to have NSHL caused by the m.1555A>G mutation of mtDNA12SrRNA gene which was close to that observed by Dai et al. (3.87%) ().

In summary, we performed the first genetic analysis of hearing loss patients from Linyi, eastern part of China. According to genetic detections of GJB2, SLC26A4, and mtDNA12SrRNA via the SNPscan assay, the fact that almost half of the patients with nonsyndromic hearing loss appeared to have a genetic etiology shows that the SNPscan assay is an available diagnosis tool for studies on genetic hearing loss. The results of the detection suggest that GJB2 mutations appear to be a major cause of congenital hearing loss in Linyi. The prevalence of SLC26A4 mutations and mtDNA12SrRNA mutations was very close to other previous studies in Chinese deaf population. However, about 50% of NSHL patients are still not identified with a molecular etiology. For this reason, copy number variations (CNVs) of the three common deafness-causing genes need to be detected. Also, next generation sequencing (NGS) will be employed in screening other deafness-causing genes in the future.

5. Conclusions

In this study, we used the SNPscan assay technique to detect the 115 mutations of the three common deafness-causing genes in 339 nonsyndromic hearing loss patients from Linyi, China. And we found that the mutation profile was distinct from other parts of China suggesting a unique mutation spectrum in this area. Also, the SNPscan assay was an available diagnosis tool for studies on genetic hearing loss.

Competing Interests

The authors declare that they have no competing interests.

Acknowledgments

This work was supported by grants from the National 973 Basic Research Program of China (2014CB541703), the Research Special Fund for Public Welfare Industry of Health (201202001), grants from the National Natural Science Foundation of China (81470693 and 81470704), a grant from the Project funded by China Postdoctoral Science Foundation (2014M560563 and 2015T80726), and grants from the Natural Science Foundation of Shandong Province (ZR2014HM022 and ZR2014HP064). The authors sincerely thank all the family members for their participation and cooperation in this study.

Supplementary Materials

All the 115 mutations of GJB2, SLC26A4, mtDNA12SrRNA detected in this study were summarized in the supplementary material.

Supplementary Material

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Copyright © 2016 Fengguo Zhang 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.

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