Characterization of a new full length TMPRSS3 isoform and identification of mutant alleles responsible for nonsyndromic recessive deafness in Newfoundland and Pakistan
- Zubair M Ahmed†1,
- Xiaoyan Cindy Li†1, 8,
- Shontell D Powell†1,
- Saima Riazuddin1,
- Terry-Lynn Young3,
- Khushnooda Ramzan2,
- Zahoor Ahmad2,
- Sandra Luscombe4,
- Kiran Dhillon5,
- Linda MacLaren6,
- Barbara Ploplis1,
- Lawrence I Shotland7, 9,
- Elizabeth Ives3,
- Sheikh Riazuddin2,
- Thomas B Friedman1,
- Robert J Morell1 and
- Edward R Wilcox1Email author
© Ahmed et al; licensee BioMed Central Ltd. 2004
Received: 06 July 2004
Accepted: 24 September 2004
Published: 24 September 2004
Mutant alleles of TMPRSS3 are associated with nonsyndromic recessive deafness (DFNB8/B10). TMPRSS3 encodes a predicted secreted serine protease, although the deduced amino acid sequence has no signal peptide. In this study, we searched for mutant alleles of TMPRSS3 in families from Pakistan and Newfoundland with recessive deafness co-segregating with DFNB8/B10 linked haplotypes and also more thoroughly characterized the genomic structure of TMPRSS3.
We enrolled families segregating recessive hearing loss from Pakistan and Newfoundland. Microsatellite markers flanking the TMPRSS3 locus were used for linkage analysis. DNA samples from participating individuals were sequenced for TMPRSS3. The structure of TMPRSS3 was characterized bioinformatically and experimentally by sequencing novel cDNA clones of TMPRSS3.
We identified mutations in TMPRSS3 in four Pakistani families with recessive, nonsyndromic congenital deafness. We also identified two recessive mutations, one of which is novel, of TMPRSS3 segregating in a six-generation extended family from Newfoundland. The spectrum of TMPRSS3 mutations is reviewed in the context of a genotype-phenotype correlation. Our study also revealed a longer isoform of TMPRSS3 with a hitherto unidentified exon encoding a signal peptide, which is expressed in several tissues.
Mutations of TMPRSS3 contribute to hearing loss in many communities worldwide and account for 1.8% (8 of 449) of Pakistani families segregating congenital deafness as an autosomal recessive trait. The newly identified TMPRSS3 isoform e will be helpful in the functional characterization of the full length protein.
Genetic analysis of inherited deafness is a powerful tool for discovering the molecular mechanisms that control the development, function and maintenance of the auditory system. Linkage analysis of deafness segregating in large families has resulted in the mapping of more than 55 non-overlapping loci and the discovery of over 30 genes that are essential for hearing . Given this extensive genetic heterogeneity, extended families from endogamous populations are ideally suited for identifying novel deafness genes and for genotype-phenotype studies.
DFNB8/B10, an autosomal recessive deafness locus, was independently mapped in two consanguineous families from Palestine and Pakistan [2, 3]. Haplotype and gene sequence analyses of individuals in these two families led to the identification of mutations in a gene encoding a serine protease, TMPRSS3 [4, 5]. TMPRSS3 belongs to a subfamily of type II transmembrane serine proteases, which also includes TMPRSS1, TMPRSS2, TMPRSS4 and TMPRSS5 . The TMPRSS3 gene, spanning approximately 24 kb on chromosome 21, contains thirteen reported exons . In humans there are alternatively spliced transcripts (TMPRSS3 a, b, c and d), encoding predicted polypeptides of 454, 327, 327 and 344 amino acids, respectively . Here, we report the identification of a fifth isoform, TMPRSS3e, which encodes 538 amino acid residues, including a signal peptide, and is expressed in many human tissues.
We previously reported pathogenic TMPRSS3 mutations in four out of a total of 159 Pakistani families segregating profound congenital recessive deafness . To determine the contribution of TMPRSS3 mutations to recessive deafness in Pakistan, we screened an additional 290 Pakistani families for linkage to the DFNB8/B10 locus. We also screened TMPRSS3 for mutations in a large kindred from Newfoundland, Canada segregating hearing loss linked to markers for DFNB8/B10 and surprisingly found two different mutant alleles.
Institutional review board approvals (OH93-N-016 and OH95-DC-N-050) were obtained for this study from the National Institutes of Health, USA, the Centre of Excellence in Molecular Biology, Lahore, Pakistan and the Newfoundland and Labrador Medical Genetics Program, Health Sciences Centre, St. John's. Participating individuals gave written informed consent. Medical histories indicated that all four Pakistani families segregate congenital, profound, non-syndromic sensorineural hearing loss. Pure tone air and bone conduction audiometry was performed on affected and unaffected individuals of the family from Newfoundland. Pneumatic otoscopy was used to confirm or deny cases in which conductive hearing loss was suspect. All testing was done in non-sound-attenuated exam room. Prior to testing, a biologic calibration was done in the room used for testing with a listener having normal hearing thresholds (LS). Possible effects of ambient noise on thresholds were then taken into account and only those frequencies unaffected were included. DNA was extracted from venous blood samples from the participating individuals.
Linkage and sequence analyses
DNA samples were PCR amplified using fluorescently labeled primers surrounding microsatellite repeats at known DFNB loci and analyzed on an ABI 377 DNA sequencer. Genotypes were determined using Genescan and Genotyper software (PE Biosystems). To detect TMPRSS3 mutations in families segregating DFNB8/B10, the sequence of each exon of TMPRSS3 was evaluated in two affected subjects from each family as described previously .
5' RACE and cloning of TMPRSS3e
Sequence analysis of the subcloned PCR product amplified from human retina GETLarge full length cDNA (Genemed Biotechnologies) using primers 5'GGGTTGCTTCAAATGGCTTACTAGATCC3' and 5'CATTTTCCCCCATGGTGACTATTTCAG revealed an additional 385 bp of transcribed sequence downstream of TMPRSS3a exon 1. 5' RACE PCR using human retina Marathon-Ready cDNA as template (Clontech) with primers 5'CAGACCAATGGCCAGTGCTAATATC3' and the AP1 primer was performed using the following thermal cycling conditions: 94°C for 1 min, 25 cycles of 94°C for 30 s and 72°C for 5 min. Five microliters of amplified PCR product was used for the second round of amplification with nested primer 5'TTTTCAAATCATCAAGGCCAAAAAG3' and the AP2 primer. Five microliters of each sample were analyzed on a 1.2% agarose/ethidium bromide gel, extracted using a QIAquick gel extraction kit (Qiagen) and cloned into E. coli using pGEM®-T Easy vector (Promega). DNA was purified from minipreps using QIAquick miniprep kit (Qiagen) and inserts were sequenced using T7 and SP6 primers. To amplify the full length TMPRSS3e isoform, 5'ATGGTGAGTAAAATGGGTGTGAGGA3' and 5'CTTGGAAGTAGAAAGGGTGGGTTTG3' primers and LA-Taq polymerase (Pan Vera) were used as recommended by the manufacturers.
Multiple-tissue cDNA panel analysis
Expression of TMPRSS3e was evaluated using a Human Tissue cDNA panel (Clontech). TMPRSS3e cDNA was amplified with primers 5'CCAGAAATGGTGAGTAAAATGG3' and 5'AGCAACAGCATCTGCATCTGGT3' using 20 pg of each cDNA as template following the manufacturer's recommended protocol (Clontech). PCR amplified products were sub-cloned into pGEM-T Easy vector (Promega) and sequenced.
Mutant alleles of TMPRSS3 found in this study
Amino acid substitution
Sequencing of the TMPRSS3 gene in affected individuals revealed two mutant alleles. The first mutation occurs in exon 4 of TMPRSS3 and is a deletion of a cytosine at position 207 (207delC) of the mRNA (Figure 1, Table 1). The second mutation inserts a "T" residue at the eighth position after the splice donor site of exon 8 (IVS8+8insT). Although the precise effect of this mutant allele is not known, Genscan predicts this results in the skipping of exon nine. Individual IV:16 is a carrier of IVS8+8insT and her two affected children are compound heterozygotes (Figure 1). Neither of these two mutations was found in 100 random normal control DNA samples (200 chromosomes) from Newfoundland.
Although the ATG codon at position 705 (Accession # AY633572) does not meet Kozak consensus criteria, there are two reasons for believing that this is the translation initiation site. First, there are stop codons in all three reading frames upstream of this site. Secondly, the 252 bp open reading frame between ATG 705 and ATG 957 (Figure 3A), the previously reported initiation codon, includes a predicted signal peptide, which is expected in a secreted serine protease. Considering the ATG at position 705 as a starting codon, analysis of the 1614 bp open reading frame indicates that this larger TMPRSS3e transcript encodes a putative polypeptide of 538 amino acids, including 84 previously unknown amino acids at the amino terminus (Figure 3B and 3C). The SMART program predicts a cleavable signal sequence between residues 1 through 36 (Figure 3A and 3B). Among all the known isoforms of TMPRSS3, only isoform e reported here has a predicted signal peptide, consistent with the hypothesis that TMPRSS3 encodes a secreted serine protease. The remaining 48 new amino acids do not contain other predicted structural or functional motifs (Figure 3A and 3B). Downstream of the newly identified 84 amino acids, isoform e shares a common protein sequence with isoform a, which includes a transmembrane (TM), low density lipoprotein receptor A (LDLRA), scavenger-receptor cysteine-rich (SRCR) and serine protease domains (Figure 3A). Through non-quantitative RT-PCR analysis with TMPRSS3e specific primers and multiple human cDNAs, we found expression of this isoform in retina, lung, liver, pancreas, placenta and kidney (Figure 3C). Mutational screening of exon 1 and exon 2 as well as other exons of TMPRSS3e, using DNA samples from two affected individuals of family PKSR7 did not reveal a pathogenic change. This may be an indication of as yet uncharacterized additional exons of TMPRSS3, or the hearing loss phenotype in this family is due to a mutation in a regulatory element of TMPRSS3. Alternatively, it remains possible that family PKSR7 has a mutation in a gene closely linked to TMPRSS3.
TMPRSS3 is the only protease reported thus far to be involved in nonsyndromic deafness . In this study, we document the mutant alleles of TMPRSS3 segregating in a large family from Newfoundland and in additional Pakistani families with nonsyndromic, recessive deafness. The Newfoundland family has at least two different mutated genes associated with hearing impairment. The majority of the affected individuals in this family are homozygous for 207delC (Figure 1), while two of the hearing impaired subjects are compound heterozygotes for 207delC and a newly described mutation of intron 8 (IVS8+8insT). The 207delC mutation appears to be wide-spread; it has been found in affected individuals of Spanish (one homozygote), Greek (one heterozygote), Newfoundland (homozygous individuals) and Pakistani (homozygous individuals, PKDF003 and PKDF311) origins, and is the most common of the mutant alleles of TMPRSS3. Although there is a predicted effect of IVS8+8insT mutation on splicing of exon 9, further studies are required to determine the precise role of IVS8+8insT on TMPRSS3 transcripts. The family from Pakistan that originally defined the DFNB8 locus was reported to have childhood onset hearing impairment , while all remaining families segregating TMPRSS3 mutations have pre-lingual deafness [4, 5, 9, 10]. Mutational screening revealed a splice site mutation (IVS4-6G>A) in the original DFNB8 family, which may allow some normal splicing of TMPRSS3 transcripts . The second mutant allele (IVS8+8insT) in the Newfoundland family may also be a leaky mutation, although the two individuals who are compound heterozygotes were described as having prelingual hearing impairment.
The hearing impaired individuals IV:10, V:2 and VI:1 of our Newfoundland family are carriers of 207delC and we did not find any other TMPRSS3 mutation in these individuals. Individuals IV:10 (affected) and IV:12 (normal hearing sibling) show an identical chromosome 21 haplotype. Similarly the individuals VI:1 (affected) and VI:2 (normal hearing sibling) share identical haplotypes for the TMPRSS3 locus. Hence, it is unlikely that the deafness of individuals IV:10 and VI:1 is due to cryptic TMPRSS3 mutations (Figure 1). As connexin 26 mutations are the most common cause of nonsyndromic recessive deafness , we sequenced the coding exon of GJB2 in affected individuals of Newfoundland family and found no mutation.
We have analyzed a total of 449 Pakistani families [ and this study] segregating severe to profound congenital recessive deafness and found a total of eight families in which the deafness phenotype is due to mutations of TMPRSS3. Therefore, the relative contribution of TMPRSS3 mutations in the deaf Pakistani population is approximately 1.8%, a significant amount considering the extensive genetic heterogeneity of deafness in this population. Of ten TMPRSS3 mutations that have been reported world wide, five (IVS4-6G>A, 207delC, R109W, C194F and C407R) are segregating in the Pakistani population [4, 5, 9, 10].
Among the ten known mutant alleles of TMPRSS3, six are present in exons common to all isoforms, including isoform "e" reported herein. Of the isoforms of this serine protease, TMPRSS3e has the longest open reading frame and is the only isoform of this gene with a predicted signal sequence at the amino terminus. The identification of 84 additional amino acids, including a predicted signal sequence, may aid functional assays to determine the role of TMPRSS3 in cochlear development and function. TMPRSS3 isoform a was identified with a forward primer (TMa-F; see supplement table B ) in exon 2 and not in exon 1 as illustrated in figure 1 of Scott et al. 2001 . Therefore, it is possible that TMPRSS3a is an incomplete version of isoform e and isoform a may not exist in vivo.
TMPRSS3 message is expressed in supporting cells of the organ of Corti, in the stria vascularis and in the spiral ganglion cells of the cochlea . Although the specific role of TMPRSS3 in the development and maintenance of the audiosensory apparatus is still unknown, the reported mutant alleles of TMPRSS3 abolish catalytic activity of the serine protease, implying a proteolytic function during the inner ear development [12, 13]. Although the in vivo substrate(s) of TMPRSS3 have not been reported in the auditory system, TMPRSS3 is thought to regulate the activity of the epithelial amiloride sensitive sodium channel (ENaC) in vitro, which was suggested to control critical signaling pathway(s) in the inner ear and may have a role in the maintenance of the low sodium concentration of endolymph . However, the absence of an abnormal auditory phenotype in individuals with Pseudohypoaldosteronism type I (PHA 1), which are homozygous for null alleles of ENaC subunits , suggests that the DFNB8/B10 deafness phenotype is due to aberrant proteolytic processing by TMPRSS3 of some other substrate in the inner ear.
TMPRSS3 mutations account for hearing loss in 1.8% (8 of 449) of Pakistani families segregating deafness as an autosomal recessive trait. We also identified two recessive mutations of TMPRSS3 segregating in a six-generation extended family from Newfoundland. Our study also revealed a longer isoform of TMPRSS3 with an exon encoding a signal peptide, which should help in the functional dissection of this secreted serine protease.
Transmembrane Protease, Serine 3 [OMIM entry 605511].
Deafness, childhood-onset neurosensory autosomal recessive 8 [OMIM entry 601072]DFNB10; Deafness, congenital neurosensory, autosomal recessive 10 [OMIM entry 605316]
We thank the families for their participation in this study, which was supported by NIDCD/NIH, Intramural Research funds Z01DC00035-06 and Z01DC00039-06. Part of this study in Pakistan was supported by Higher Education Commission, Islamabad, Pakistan and by International Centre for Genetic Engineering and Biotechnology, Trieste, Italy under Project CRP/PAK02-01 (Contract No.02/013). We thank Shaheen Khan, Tamar Ben-Yosef, Juile Schultz and Dennis Drayna for advice and comments in preparing the manuscript.
- Friedman TB, Griffith AJ: Human nonsyndromic sensorineural deafness. Annu Rev Genomics Hum Genet. 2003, 4: 341-402. 10.1146/annurev.genom.4.070802.110347.View ArticlePubMedGoogle Scholar
- Bonne-Tamir B, DeStefano AL, Briggs CE, Adair R, Franklyn B, Weiss S, Korostishevsky M, Frydman M, Baldwin CT, Farrer LA: Linkage of congenital recessive deafness (gene DFNB10) to chromosome 21q22.3. Am J Hum Genet. 1996, 58: 1254-1259.PubMedPubMed CentralGoogle Scholar
- Veske A, Oehlmann R, Younus F, Mohyuddin A, Muller-Myhsok B, Mehdi SQ, Gal A: Autosomal recessive non-syndromic deafness locus (DFNB8) maps on chromosome 21q22 in a large consanguineous kindred from Pakistan. Hum Mol Genet. 1996, 5: 165-168. 10.1093/hmg/5.1.165.View ArticlePubMedGoogle Scholar
- Scott HS, Kudoh J, Wattenhofer M, Shibuya K, Berry A, Chrast R, Guipponi M, Wang J, Kawasaki K, Asakawa S, Minoshima S, Younus F, Mehdi SQ, Radhakrishna U, Papasavvas MP, Gehrig C, Rossier C, Korostishevsky M, Gal A, Shimizu N, Bonne-Tamir B, Antonarakis SE: Insertion of beta-satellite repeats identifies a transmembrane protease causing both congenital and childhood onset autosomal recessive deafness. Nat Genet. 2001, 27: 59-63.PubMedGoogle Scholar
- Ben-Yosef T, Wattenhofer M, Riazuddin S, Ahmed ZM, Scott HS, Kudoh J, Shibuya K, Antonarakis SE, Bonne-Tamir B, Radhakrishna U, Naz S, Ahmed Z, Pandya A, Nance WE, Wilcox ER, Friedman TB, Morell RJ: Novel mutations of TMPRSS3 in four DFNB8/B10 families segregating congenital autosomal recessive deafness. J Med Genet. 2001, 38: 396-400. 10.1136/jmg.38.6.396.View ArticlePubMedPubMed CentralGoogle Scholar
- Szabo R, Wu Q, Dickson RB, Netzel-Arnett S, Antalis TM, Bugge TH: Type II transmembrane serine proteases. Thromb Haemost. 2003, 90: 185-193.PubMedGoogle Scholar
- Ives E, Collis E: Severe childhood deafness on Newfoundland's south coast. Am J Hum Genet. 1991, Supp 49: 142-Google Scholar
- Rahman P, Jones A, Curtis J, Bartlett S, Peddle L, Fernandez BA, Freimer NB: The Newfoundland population: a unique resource for genetic investigation of complex diseases. Hum Mol Genet. 2003, 12 Spec No 2: R167-72. 10.1093/hmg/ddg257.View ArticlePubMedGoogle Scholar
- Wattenhofer M, Di Iorio MV, Rabionet R, Dougherty L, Pampanos A, Schwede T, Montserrat-Sentis B, Arbones ML, Iliades T, Pasquadibisceglie A, D'Amelio M, Alwan S, Rossier C, Dahl HH, Petersen MB, Estivill X, Gasparini P, Scott HS, Antonarakis SE: Mutations in the TMPRSS3 gene are a rare cause of childhood nonsyndromic deafness in Caucasian patients. J Mol Med. 2002, 80: 124-131. 10.1007/s00109-001-0310-6.View ArticlePubMedGoogle Scholar
- Masmoudi S, Antonarakis SE, Schwede T, Ghorbel AM, Gratri M, Pappasavas MP, Drira M, Elgaied-Boulila A, Wattenhofer M, Rossier C, Scott HS, Ayadi H, Guipponi M: Novel missense mutations of TMPRSS3 in two consanguineous Tunisian families with non-syndromic autosomal recessive deafness. Hum Mutat. 2001, 18: 101-108. 10.1002/humu.1159.View ArticlePubMedGoogle Scholar
- Cryns K, Orzan E, Murgia A, Huygen PL, Moreno F, del Castillo I, Chamberlin GP, Azaiez H, Prasad S, Cucci RA, Leonardi E, Snoeckx RL, Govaerts PJ, Van de Heyning PH, Van de Heyning CM, Smith RJ, Van Camp G: A genotype-phenotype correlation for GJB2 (connexin 26) deafness. J Med Genet. 2004, 41: 147-154. 10.1136/jmg.2003.013896.View ArticlePubMedPubMed CentralGoogle Scholar
- Guipponi M, Vuagniaux G, Wattenhofer M, Shibuya K, Vazquez M, Dougherty L, Scamuffa N, Guida E, Okui M, Rossier C, Hancock M, Buchet K, Reymond A, Hummler E, Marzella PL, Kudoh J, Shimizu N, Scott HS, Antonarakis SE, Rossier BC: The transmembrane serine protease (TMPRSS3) mutated in deafness DFNB8/10 activates the epithelial sodium channel (ENaC) in vitro. Hum Mol Genet. 2002, 11: 2829-2836. 10.1093/hmg/11.23.2829.View ArticlePubMedGoogle Scholar
- Lee YJ, Park D, Kim SY, Park WJ: Pathogenic mutations but not polymorphisms in congenital and childhood onset autosomal recessive deafness disrupt the proteolytic activity of TMPRSS3. J Med Genet. 2003, 40: 629-631. 10.1136/jmg.40.8.629.View ArticlePubMedPubMed CentralGoogle Scholar
- Chang SS, Grunder S, Hanukoglu A, Rosler A, Mathew PM, Hanukoglu I, Schild L, Lu Y, Shimkets RA, Nelson-Williams C, Rossier BC, Lifton RP: Mutations in subunits of the epithelial sodium channel cause salt wasting with hyperkalaemic acidosis, pseudohypoaldosteronism type 1. Nat Genet. 1996, 12: 248-253. 10.1038/ng0396-248.View ArticlePubMedGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2350/5/24/prepub
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