Prevalence of the GJB2 IVS1+1G >A mutation in Chinese hearing loss patients with monoallelic pathogenic mutation in the coding region of GJB2
- Yongyi Yuan†1,
- Fei Yu†1,
- Guojian Wang†1, 1,
- Shasha Huang1,
- Ruili Yu1,
- Xin Zhang1,
- Deliang Huang1Email author,
- Dongyi Han1Email author and
- Pu Dai1Email author
© Yuan et al; licensee BioMed Central Ltd. 2010
Received: 9 September 2010
Accepted: 2 December 2010
Published: 2 December 2010
Mutations in the GJB2 gene are the most common cause of nonsyndromic recessive hearing loss in China. In about 6% of Chinese patients with severe to profound sensorineural hearing impairment, only monoallelic GJB2 mutations known to be either recessive or of unclear pathogenicity have been identified. This paper reports the prevalence of the GJB2 IVS1+1G>A mutation in a population of Chinese hearing loss patients with monoallelic pathogenic mutation in the coding region of GJB2.
Two hundred and twelve patients, screened from 7133 cases of nonsyndromic hearing loss in China, with monoallelic mutation (mainly frameshift and nonsense mutation) in the coding region of GJB2 were examined for the GJB2 IVS1+1G>A mutation and mutations in the promoter region of this gene. Two hundred and sixty-two nonsyndromic hearing loss patients without GJB2 mutation and 105 controls with normal hearing were also tested for the GJB2 IVS1+1G>A mutation by sequencing.
Four patients with monoallelic mutation in the coding region of GJB2 were found carrying the GJB2 IVS1+1G>A mutation on the opposite allele. One patient with the GJB2 c.235delC mutation carried one variant, -3175 C>T, in exon 1 of GJB2. Neither GJB2 IVS1+1G>A mutation nor any variant in exon 1 of GJB2 was found in the 262 nonsyndromic hearing loss patients without GJB2 mutation or in the 105 normal hearing controls.
Testing for the GJB2 IVS 1+1 G to A mutation explained deafness in 1.89% of Chinese GJB2 monoallelic patients, and it should be included in routine testing of patients with GJB2 monoallelic pathogenic mutation.
Hereditary hearing loss is a genetically heterogeneous disorder in humans, with an incidence rate of approximately 1 in 1000 children . Nonsyndromic deafness accounts for 60-70% of cases of inherited hearing impairment and involves 114 loci and 55 different genes with autosomal dominant (DFNA), autosomal recessive (DNFB), X-linked (DFN), and maternal inheritance patterns . The most common causes of nonsyndromic autosomal recessive hearing loss are mutations in connexin 26, a gap-junction protein encoded by the GJB2 gene [3–10].
To date, more than 150 mutations, polymorphisms, and unclassified variants have been described in the GJB2 gene, which account for the molecular etiology of 10-50% of patients with nonsyndromic hearing impairment http://davinci.crg.es/deafness. Therefore, GJB2 is normally the first gene to be tested in patients with hearing loss. In China, the ratio of patients carrying mutations in the coding exons of GJB2 is 21% (biallelic, 14.9%; monoallelic, 6.1%) . However, few studies have examined the noncoding exon 1 of GJB2 in Chinese hearing-impaired patients, and even fewer studies have investigated the promoter region of this gene. The results of GJB2 screening performed to date have indicated that a substantial fraction of patients (6-15%) carry only one pathogenic mutation in the GJB2 gene with either recessive or unclear pathogenicity, despite direct sequencing of the entire coding region of the gene [12–14]. The ratio of a 309-kb deletion involving the GJB6 gene, now called del(GJB6-D13S1830), was shown to be the second causal mutation in these monoallelic heterozygous patients in Spain and France [15, 16]. Previously, we tested Chinese patients with only one monoallelic mutation in the coding region of GJB2 for the presence of this mutation, but the results indicated this to be a very rare cause of hearing loss in the Chinese population, and this is not a major additional factor in our monoallelic patients (unpublished). Similar results have also been reported in Austria and the Czech Republic [17, 18]. The splice site mutation IVS1+1G>A, also called the -3170 G>A mutation, in the GJB2 gene was originally reported by Denoyelle et al. . This splice site mutation has been found in several populations [20–26] and is predicted to disrupt splicing, yielding no detectable mRNA . Not all genetic laboratories routinely test for this mutation, which lies outside the coding region of the GJB2 gene. This study focused on clarifying the impact of GJB2 IVS1+1G>A mutation and the promoter region of this gene among Chinese patients with hearing loss, especially those with pathogenic mutation in only one allele of the GJB2 gene coding region.
Materials and methods
Patients and DNA samples
GJB2 IVS1+1G>A mutation in Chinese hearing loss patients with monoallelic pathogenic mutation in GJB2
Exon 1 or splice site
or amino acid
or amino acid
Splicing site mutation
Splicing site mutation
Splicing site mutation
The 212 deaf patients consisted of 123 males and 90 females from 0.2 to 67 years old, with an average age of 5.41 ± 1.78 years. Ethnically, the patients consisted of 196 Han, 4 Hui, 3 Uygur, 3 Mongolian, 2 Tibetan, 2 Maan, 1 Miao, 1 Chuang, and 1 Buyi Chinese.
The 262 unrelated nonsyndromic hearing loss patients without GJB2 coding region mutation were selected randomly from patients of the Genetic Testing Center for Deafness, PLA General Hospital, during the year 2007. This cohort consisted of 147 males and 115 females from 2 to 46 years old with an average age of 4.52 ± 1.16 years, and ethnically, they were all Han Chinese.
The study protocol was performed with the approval of the Ethics Committee of the Chinese PLA General Hospital. Informed consent was obtained from all subjects prior to blood sampling. The parents of pediatric patients were interviewed with regard to age of onset, family history, mother's health during pregnancy, and patient's clinical history, including infection, possible head or brain injury, and the use of aminoglycoside antibiotics. All subjects showed moderate to profound bilateral sensorineural hearing impairment on audiograms. Careful medical examinations revealed no clinical features other than hearing impairment. DNA was extracted from the peripheral blood leukocytes of the 474 (212 + 262) patients with nonsyndromic hearing loss and 105 controls with normal hearing using a commercially available DNA extraction kit (Watson Biotechnologies Inc., Shanghai, China).
The coding exon (exon 2) and flanking intronic regions of GJB2 gene were amplified by PCR with the primers F (5'TTG-GTG-TTT-GCT-CAG-GAA-GA-3') and R (5'GGC-CTA-CAG-GGG-TTT-CAA-AT-3') in all 7133 nonsyndromic hearing loss cases. The GJB2 exon 1, its flanking donor splice site and the GJB2 basal promoter were amplified with the primers F (5'CTC-ATG-GGG-GCT-CAA-AGG-AAC-TAG-GAG-ATC-GG-3') and R (5'GGG-GCT-GGA-CCA-ACA-CAC-GTC-CTT-GGG-3') in all subjects with monoallelic mutation in the coding region of GJB2, 262 unrelated nonsyndromic hearing loss patients without GJB2 mutation, and 105 normal controls.
All the patients and controls were also tested for GJB6 309-kb deletion and the coding exon of GJB6. The presence of the 309-kb deletion of GJB6 was analyzed by PCR [15, 27]. A positive control (provided by Balin Wu, Department of Laboratory Medicine, Children's Hospital Boston and Harvard Medical School, Boston, MA) was used for detection of GJB6 gene deletions. The coding exon of GJB6 was amplified with the primers F (5' TTG-GCT-TCA-GTC-TGT-AAT-ATC-ACC-3') and R (5' TCA-TTT-ACA-AAC-TCT-TCA-GGC-TAC-AG-3'). All the PCR products were purified on Qia-quick spin columns (Qiagen, Valencia, CA) and sequenced using a BigDye Terminator Cycle Sequencing kit (version v.3.1) and ABI 3130 automated DNA sequencer (Applied Biosystems, Foster City, CA) with sequence-analysis software (Sequencing Analysis version v.3.7) according to the manufacturer's protocol.
Mitochondrial 12S rRNA and SLC26A4 were also sequenced in the 262 unrelated nonsyndromic hearing loss patients without GJB2 coding region mutation. DNA sequence analysis of mitochondrial 12S rRNA and SLC26A4 were performed by PCR amplification of the coding exons plus approximated 50-100 bp of the flanking intron regions followed by Big Dye sequencing and analysis using ABI 3100 DNA sequencing machine (ABI, Foster City, USA.) and ABI 3100 Analysis Software v.3.7 NT according to manufacturer's procedures.
Deafness in 10.8%(767/7133) of the 7133 nonsyndromic hearing loss patients is postlingual and in 89.2% (6366/7133) is preligual. The percent of postlingual hearing loss in the 212 nonsyndromic hearing loss patients group with monoallelic mutation in the coding region of GJB2 is 6.6%(14/212) and that of preligual is 93.4% (198/212). The percent of postlingual hearing loss in the 262 nonsyndromic hearing loss patients group without GJB2 coding region mutation is 8%(21/262) and that of preligual is 92% (241/262). The average onset age of postlingual hearing loss in the 7133 patient cohort is 3.19 ± 1.56 years, and that age in the 212 patient group with monoallelic mutation in the coding region of GJB2 and the 262 patient group without GJB2 coding region mutation is 2.78 ± 1.06 years and 3.04 ± 2.39 years, respectively.
All of the 212 unrelated patients with monoallelic GJB2 coding region mutation as well as the 262 unrelated nonsyndromic hearing loss patients without GJB2 coding region mutation showed bilateral moderate to profound sensorineural hearing loss. None of the patients in this study showed clinical signs in any other organs except hearing impairment.
Mutations of GJB2 Exon 1 in Chinese hearing loss patients with monoallelic pathogenic mutation in GJB2
Genotype of the proband (EXON 1/EXON 2)
Genotype of the proband's father
Genotype of the proband's mother
Genotype of the proband's siblings
No blood sample
No blood sample
No blood sample
No blood sample
Among the 262 patients without GJB2 mutation, four carried the mitochondrial 12S rRNA A1555G mutation, and 19 carried SLC26A4 mutations and were diagnosed as having enlarged vestibular aqueduct by temporal CT scan. None of these patients was found to carry the GJB2 IVS1+1G>A mutation. One patient was shown to carry the GJB6 c.404C>A mutation (T135K), and this patient had no mutation in mitochondrial 12S rRNA or SLC26A4. This patient was of the Uygur ethnic minority from Xinjiang Uyghur Autonomous Region.
In the control group, we detected two c.235delC and one c.299delAT heterozygotes, representing 3%, which coincided with our previous results in a different control cohort . No GJB2 IVS1+1G>A mutation was detected in the control group. A GJB6 variant, c.446 C>T mutation (A149V), was detected in an individual of the Uygur ethnic minority.
We did not find the 309-kb deletion of GJB6 in any of the 212 patients with monoallelic GJB2 coding region mutation or in any of the 105 samples from normal hearing controls with no history of hearing loss.
The GJB2 gene is composed of two exons separated by an intron, and the coding region is entirely contained in exon 2. The basal promoter activity resides in the first 128 nucleotides upstream of the transcription start point (TSP) and has two GC boxes, at positions 281 and 293 from the TSP, which are important for transcription . Most of the GJB2 sequence variations described to date are localized in the coding region, and only a few have been reported in noncoding regions of the gene [19, 23, 29–31]. Mutational screening performed to date has usually focused on the coding region. GJB2 is responsible for up to 21% of cases of deafness in the Chinese population . The most common mutation is a frameshift mutation due to deletion of a single cytosine at position 235 (235delC). The four most prevalent mutations: c.235delC, c.299_c.300delAT, c.176_c.191del16, and c.35delG, account for 88.0% of all mutant GJB2 alleles identified in China .
Sequence analysis of the GJB2 gene in subjects with autosomal recessive hearing impairment has revealed a puzzling problem in that a large proportion of patients (6-15%) carry only one mutant allele [14–17]. Some of these families showed clear evidence of linkage to the DFNB1 locus, which contains two genes, GJB2 and GJB6. Further analysis demonstrated a 309-kb deletion, truncating the GJB6 gene, encoding connexin 30, near GJB2 in heterozygous affected subjects [18, 19]. We had tested Chinese patients with only one monoallelic mutation in the coding region of GJB2 for the presence of this deletion, but it was shown to be a very rare cause of deafness in the Chinese population. Similar results in populations in Turkey, Iran, Austria, Taiwan, China, Poland, and the Altai Republic have also been reported [25, 32–39]. Cases with one pathogenic mutation in the GJB2 gene may have another as yet unidentified pathogenic mutation in the promoter region or other noncoding regions of GJB2.
To evaluate the impact of the IVS1+1G>A splice-site mutation and the basal promoter region in the noncoding part of the GJB2 gene among Chinese patients, we initially carried the sequencing of GJB2 exon1 among 851 deaf individuals from Central China and no mutation was found, which suggested very low detection rate of GJB2 exon1 mutation among Chinese deaf population. Thus we began to collect and test all available nonsyndromic hearing loss patients with only one monoallelic pathogenic mutation in the coding part of GJB2. By sequencing exon 1 and the basal promoter region of the GJB2 gene in 212 Chinese patients with GJB2 monoallelic mutation, we identified four patients carrying the IVS1+1G>A mutation. Testing for this mutation explained deafness in 1.89% of Chinese GJB2 monoallelic patients. This ratio is significantly lower than the value of 45% in Czech patients with one pathogenic mutation in GJB2 and 23.40% of Hungarian patients carrying a mutation in only one allele of the coding region of the GJB2 gene . It is also lower than the value of 4.6% among Brazilian patients with one pathogenic GJB2 mutation . The percentage of the IVS1+1G>A mutation was 1.85% (4/216) of mutant alleles in our patient cohort, while in the Kurdish deaf population this percentage is 9.4%(3/32), significantly higher than the Chinese population. As for the Mongolian population, the frequency of deaf probands carrying two GJB2 pathogenic mutations was 4.5%, significantly lower than that (14.9%) in the Chinese deaf population and the mutation spectrums of GJB2 is also different from that in China. The most common mutation in GJB2 was IVS1+1G to A with an allele frequency of 3.5% in the Mongolian deaf population. While c.235delC was the most common mutation in the Chinese deaf population with an allele frequency of 12.34%, significantly higher than that in the Mongolian deaf population which was 1.5%. The differences between the two Asian neighboring countries may lie in two aspects: a) the genetic background of the two races varies. b) in our study IVS1 +1G to A mutation was only screened in hearing loss patients with monoallelic mutation (mainly frameshift and nonsense mutation) in the coding region of GJB2. These observations indicate that the carrying rate of GJB2 IVS1+1G>A mutation varies among different races. We also tested the IVS1+1G>A mutation in 262 unrelated nonsyndromic hearing loss patients without GJB2 ORF mutation and 105 normal controls, but neither homozygous IVS1+1G>A mutation nor heterozygous IVS1+1G>A mutation was found. The IVS1+1G>A mutation may account for the genetic etiology only in patients with GJB2 monoallelic pathogenic mutation in the Chinese deaf population, which suggests that the frequency of IVS1+1G>A mutation is very low in Chinese population.
Matos et al.  reported a GJB2 mutation, -3438C>T, located in the basal promoter of the gene, in trans with V84M, in a patient with profound hearing impairment. They verified that the -3438C>T mutation can abolish the basal promoter activity of GJB2. Although we extended mutational screening to regions of GJB2 exon 1, its flanking donor splice site, and the GJB2 basal promoter, we found no other mutation except one c.-3175C>T variant in exon 1 and four heterozygous IVS1+1G>A mutations. As the variant, c.-3175C>T, is in the noncoding region, it was taken to be nonpathogenic.
In this study, we only counted pathogenic mutations, frameshift mutations, and nonsense pathogenic mutations; if all the missense mutations which was not found or the carrier rate was significantly low in the normal hearing controls, were calculated, the rate was increased to 5.5%.
Additionally, about 13% of patients had moderate hearing loss, whereas all the patients in our previous study  showed severe to profound hearing impairment.
Through genotype and phenotype analysis in 1093 cases of unrelated, nonsyndromic Chinese individuals with hearing loss, GJB2 mutations were detected in 24.67% (130/527) of patients with bilateral profound hearing loss, 22.33% (44/197) with bilateral severe hearing loss, 14.33% (42/293) with bilateral moderate hearing loss, and 6.58% (5/76) with bilateral mild hearing loss (unpublished data). The differences between the severe to profound hearing loss group and the mild to moderate hearing loss group were statistically significant. In this patient group, the total percentage of GJB2 mutations in all the 1093 cases is 20.22%(221/1093), similar to that in our previous study. Additionally, patients in the above two cohorts didn't overlap.
The second mutant allele has not yet been identified due to the location of mutations deep in introns that were not sequenced.
It is possible that a digenic pattern of inheritance is responsible for these cases. Therefore, the second mutation may be a connexin gene other than GJB6 or may involve another gene, the product of which interacts with connexin 26. Clearly, this hypothesis can not be verified until the other mutant alleles have been found.
Part of these heterozygous probands are simply carriers, and their hearing impairment may have other causes.
Testing for the GJB2 IVS 1+1 G to A mutation explained deafness in 1.89% of Chinese GJB2 monoallelic patients. Although the percentage is not as high as those in Western and Mongolian populations, it can still serve as a routine testing point in patients with GJB2 monoallelic pathogenic mutation in China.
Conflict of interest statement
The authors declare that they have no competing interests.
This work was supported by Chinese National Nature Science Foundation Research Grant (30572015, 30728030, 31071109), Beijing Nature Science Foundation Research Grant (7062062) to Dr. Pu Dai, Chinese National Nature Science Foundation Research Grant (30801285) and Beijing Nova programme (2009B34) to Dr. Yongyi Yuan.
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