Identification of a Novel MYO15A Mutation in a Chinese Family with Autosomal Recessive Nonsyndromic Hearing Loss

Autosomal recessive nonsyndromic hearing loss (ARNSHL) is a genetically heterogeneous sensorineural disorder, generally manifested with prelingual hearing loss and absence of other clinical manifestations. The aim of this study is to identify the pathogenic gene in a four-generation consanguineous Chinese family with ARNSHL. A novel homozygous variant, c.9316dupC (p.H3106Pfs*2), in the myoxin XVa gene (MYO15A) was identified by exome sequencing and Sanger sequencing. The homozygous MYO15A c.9316dupC variant co-segregated with the phenotypes in the ARNSHL family and was absent in two hundred normal controls. The variant was predicted to interfere with the formation of the Myosin XVa-whirlin-Eps8 complex at the tip of stereocilia, which is indispensable for stereocilia elongation. Our data suggest that the homozygous MYO15A c.9316dupC variant might be the pathogenic mutation, and exome sequencing is a powerful molecular diagnostic strategy for ARNSHL, an extremely heterogeneous disorder. Our findings extend the mutation spectrum of the MYO15A gene and have important implications for genetic counseling for the family.


Introduction
Congenital or prelingual hearing loss is a common sensorineural disorder, with a prevalence of about one in 500-1,000 at birth, and at least half of the cases are caused by genetic factors [1,2]. At least 70% of the cases manifest with isolated hearing loss without other associated clinical features, which is classified as nonsyndromic deafness [3]. Hereditary hearing loss mainly displays autosomal recessive or autosomal dominant transmission [2], and X-linked [4] or mitochondrial inheritance [5] is occasionally reported. Most of hereditary deafness manifests as autosomal recessive nonsyndromic hearing loss (ARNSHL) [3]. ARNSHL is an extremely heterogeneous disease, generally manifested with congenital or prelingual hearing loss without associated clinical symptoms, though postlingual hearing loss has also been reported [2,6]. The individuals with early-onset deafness often encounter obstacles for linguistic development [7]. Since identification of the gap junction protein beta-2 gene (GJB2) as the disease gene for ARNSHL [8], more than 42 genes have been identified and at least 1,949 pathogenic variants have been reported [9]. Mutations in these genes affect cochlear homeostasis, cellular organization, neuronal transmission, cell growth, differentiation and survival, and tectorial membrane associated proteins [2]. Cochlear implantation has been reported to offer satisfactory auditory performance to patients with severe to profound deafness caused by mutations in the GJB2 gene, the solute carrier family 26 member 4 gene (SLC26A4), the otoferlin gene (OTOF) [10], or the myosin XVa gene (MYO15A) [11]. Genetic diagnosis plays an important role in prognosis evaluation, clinical management, and prenatal diagnosis for ARNSHL families [12].
It is difficult to identify causative mutations using regular Sanger sequencing because of high heterogeneity of ARNSHL. Recently, exome sequencing has been introduced and confirmed as an effective alternative strategy [13]. In this study, a novel homozygous mutation in the MYO15A gene was identified in a Chinese ARNSHL family by exome sequencing.

Subjects
A four-generation consanguineous Chinese Han family with ARNSHL was recruited, and four members of the family participated in this study. Bilateral prelingual deafness was observed in the two siblings (IV:1 and IV:2, Fig 1A), who received neither hearing aids nor cochlear implantation in their childhood. However, their parents (III:1 and III:2, Fig 1A) had normal hearing. Two hundred ethnically-matched unrelated subjects (age 29.5±6.5 years) with normal hearing were enrolled as controls. Clinical and audiometric assessments were performed, and peripheral blood samples were collected from all the subjects after obtaining written informed consent from the participants or guardians. The study was approved by the Institutional Review Board of the Third Xiangya Hospital, Central South University, China.

Whole exome sequencing and variant analysis
Genomic DNA was extracted from peripheral blood samples of all the subjects using standard phenol-chloroform extraction method [15]. Exome sequencing was conducted by Novogene Bioinformatics Institute, Beijing, China. At least 1.5 micrograms (μg) of genomic DNA from the proband (IV:2, Fig 1A) was sheared by Covaris sonicators, and was enriched, hybridized, and captured on the Agilent SureSelect Human All Exon V5, following the manufacturers' procedures. The captured library was sequenced with the Illumina HiSeq 2000 sequencing instruments. The average sequencing depth of 57.36× provided enough depth to exactly call variants at 97.4% of targeted exome [16].

Direct Sanger sequencing and functional prediction
Direct Sanger sequencing was performed to confirm potential causative variants in the family with ABI3500 sequencer (Applied Biosystems, Foster City, CA, USA) [21]. Primer sequences for pathogenic variant in the MYO15A gene (NM_016239.3) were designed as follows: 5 0 - TGCCCACCCTGTTCTTATGT -3 0 and 5 0 -ACTCACTGCTTGGAGCTGGT-3 0 . MutationTaster was applied to the functional prediction of the MYO15A pathogenic variant [22].

Clinical findings
Both patients (IV:1 and IV:2, Fig 1A) presented with deafness and dumbness. Bilateral profound sensorineural hearing loss with thresholds over 95 dBHL was revealed by PTA. Type A tympanometric curve was shown by acoustic immitance measurement, and no inner ear anomaly was discovered by MRI in the two patients. The ABR at 97 dB, AR, TEOAE and DPOAE were absent in both ears of the proband (IV:2, Fig 1A) and the right ear of the elder sibling (IV:1, Fig 1A), while the waves I, III and V of ABR were elicited at 80 dB, remarkably elevated acoustic reflex threshold (80-105 dB) was recorded, and low amplitude DPOAE was elicited at 500, 1000 and 4000 Hz in the left ear of the IV:1 patient, which suggested that some residual hearing might exist in the left ear of the IV:1 patient. The clinical information of the ARNSHL family was summarized in Table 1.

Exome sequencing
A total of 19,816,364 pairs of sequenced reads with the average read length of 125 bp were generated by exome sequencing, and 98.76% (19,569,878) of sequenced reads passed the quality assessment and were mapped to 99.81% of the human reference genome [16]. Known variants identified in dbSNP142 with minor allele frequency (MAF) >1%, 1000 Genomes Project with a frequency of >0.5%, and NHLBI ESP6500 were filtered out. PolyPhen-2 and SIFT were applied to predict functional effects of non-synonymous SNPs. Subsequently, a homozygous MYO15A c.9316dupC variant was observed in the proband (IV:2, Fig 1A and 1B) and other possible pathogenic mutations for ARNSHL were excluded.

Identification of pathogenic mutation
The homozygous MYO15A c.9316dupC variant was confirmed by Sanger sequencing. The same homozygous MYO15A variant was also detected in his affected sibling (IV:1, Fig 1A), and the heterozygous MYO15A c.9316dupC variant was identified in both of his unaffected parents (III:1 and III:2, Fig 1A and 1C). However, the variant was absent in two hundred ethnicallymatched unrelated controls (Fig 1D). The homozygous MYO15A c.9316dupC variant, which co-segregated with the phenotype of deafness and dumbness in the family, and was predicted to lead to a shift in the reading frame at amino acid position 3106 and a premature stop codon (p.H3106Pfs Ã 2) by MutationTaster [22], might be the disease-causing mutation in the ARNSHL family.

Discussion
In 1995, a disease gene locus (deafness, autosomal recessive 3; DFNB3) for ARNSHL was first mapped to chromosome 17p-17q12 by linkage analysis of two large multi-generation families from Bengkala, Bali [23], and then was further refined to chromosome 17p11.2 [24]. In 1998, the homozygous p.N2111Y, p.I2113F and p.K2601 Ã (previously known as p.N890Y, p.I892F and p.K1300 Ã ) mutations in the MYO15A gene were identified in three unrelated DFNB3 families [25,26]. A hemizygous p.T2205I mutation of the MYO15A gene was also reported to be associated with moderately severe hearing loss in a Smith-Magenis syndrome (del(17)p11.2) patient [27]. Homozygous MYO15A mutations cause 6.2% of ARNSHL in Turkey [3], and mutations in the MYO15A gene account for no less than 5% of autosomal recessive profound hearing loss in Pakistan [27]. To date, at least 86 pathogenic variants of the MYO15A gene have been reported in deafness populations [3,11,, which are summarized in Fig 2. The p.D2720H mutation in the MYO15A gene is considered as a founder mutation in Pakistan [46], and the p. R1937Tfs Ã 10 and p.S3335Afs Ã 121 mutations in the MYO15A gene were also identified as founder mutations in Turkish population [3]. Most mutations in the MYO15A gene are connected with congenital severe to profound sensorineural deafness [27,46], while some patients also display progressive hearing loss [11,36]. Intriguingly, a homozygous p.Y289 Ã mutation in the MYO15A gene was associated with maintenance of considerable residual hearing in two Turkish patients [3]. High frequency hearing loss or retention of some hearing at low frequency was also reported in patients with MYO15A mutations [11,46]. The MYO15A gene contains 66 exons and encodes several alternatively spliced transcripts in the inner ear [25]. The complete transcript consists of 3530 amino acids, including a long Nterminal extension encoded by exon 2, an N-terminal motor domain, two light chain binding IQ motifs, and a tail region containing two myosin-tail homology 4 (MyTH4) domains, two band 4.1/ezrin/radixin/moesin (FERM) domains, a Src-homology-3 (SH3) domain and a Cterminal class I PDZ-ligand domain [25,48]. Myosin XVa protein is mainly expressed in the cuticular plate and stereocilia of the cochlear inner and outer hair cells [25], and is commonly localized at the tips of inner ear sensory cell stereocilia [49]. Myosin XVa is involved in staircase formation of the hair bundle, which is indispensable to sound detecting and head movement [48,49].
Homozygous p.C1779Y mutation in the Myo15 gene, a murine homologue of the human MYO15A gene, cause profound sensorineural deafness, vestibular defects, and extremely short stereocilia on the inner and outer hair cells in shaker-2 mice [50].
In this study, the homozygous c.9316dupC variant in the MYO15A gene was identified in the two affected siblings, but was absent in the unaffected parents and two hundred normal controls. The homozygous c.9316dupC variant in the MYO15A gene co-segregated with the phenotype of deafness in the ARNSHL family and might be the disease-causing mutation.
Both affected siblings display bilateral prelingual, profound sensorineural hearing loss, in accordance with most MYO15A-associated ARNSHL phenotypes [3]. Their language acquisitions were hindered by profound prelingual deafness [7], thus they also present with dumbness phenotypes. The audiometric tests of the IV:1 patient implied that the patient might have some residual hearing, consistent with the previous report [46].
The novel c.9316dupC variant in the MYO15A gene, located in the second MyTH4 domain [43], was predicted to result in a shift in the reading frame and a premature stop codon (p. H3106Pfs Ã 2) by MutationTaster [22], which leads to a truncated protein missing part of the second MyTH4 domain, the second FERM domain and PDZ-ligand in the tail region of myosin XVa (Fig 2). More than ten mutations have been reported in the second MyTH4 and FERM domain of myosin XVa (summarized in Fig 2). The MyTH4-FERM region is involved in formation of the Myosin XVa-whirlin-Eps8 complex [51] and microtubule binding [52]. Thus, the c.9316dupC variant in the MYO15A gene might interfere with formation of the Myosin XVa-whirlin-Eps8 complex, which is indispensable for stereocilia elongation and sound detecting [48,51].

Conclusion
The homozygous c.9316dupC variant in the MYO15A gene was the pathogenic mutation in our ARNSHL family. Our study demonstrated that exome sequencing is a powerful molecular diagnostic strategy for ARNSHL, an extremely heterogeneous genetic disorder. Our findings extend the mutation spectrum of the MYO15A gene, and have implication in genetic counseling for the ARNSHL family.