Neuhaus, Christine and Eisenberger, Tobias and Decker, Christian and Nagl, Sandra and Blank, Cornelia and Pfister, Markus and Kennerknecht, Ingo and Mueller-Hofstede, Cornelie and Issa, Peter Charbel and Heller, Raoul and Beck, Bodo and Ruether, Klaus and Mitter, Diana and Rohrschneider, Klaus and Steinhauer, Ute and Korbmacher, Heike M. and Huhle, Dagmar and Elsayed, Solaf M. and Taha, Hesham M. and Baig, Shahid M. and Stoehr, Heidi and Preising, Markus and Markus, Susanne and Moeller, Fabian and Lorenz, Birgit and Nagel-Wolfrum, Kerstin and Khan, Arif O. and Bolz, Hanno J. (2017) Next-generation sequencing reveals the mutational landscape of clinically diagnosed Usher syndrome: copy number variations, phenocopies, a predominant target for translational read-through, and PEX26 mutated in Heimler syndrome. MOLECULAR GENETICS & GENOMIC MEDICINE, 5 (5). pp. 531-552. ISSN 2324-9269,
Full text not available from this repository. (Request a copy)Abstract
BackgroundCombined retinal degeneration and sensorineural hearing impairment is mostly due to autosomal recessive Usher syndrome (USH1: congenital deafness, early retinitis pigmentosa (RP); USH2: progressive hearing impairment, RP). MethodsSanger sequencing and NGS of 112 genes (Usher syndrome, nonsyndromic deafness, overlapping conditions), MLPA, and array-CGH were conducted in 138 patients clinically diagnosed with Usher syndrome. ResultsA molecular diagnosis was achieved in 97% of both USH1 and USH2 patients, with biallelic mutations in 97% (USH1) and 90% (USH2), respectively. Quantitative readout reliably detected CNVs (confirmed by MLPA or array-CGH), qualifying targeted NGS as one tool for detecting point mutations and CNVs. CNVs accounted for 10% of identified USH2A alleles, often in trans to seemingly monoallelic point mutations. We demonstrate PTC124-induced read-through of the common p.Trp3955* nonsense mutation (13% of detected USH2A alleles), a potential therapy target. Usher gene mutations were found in most patients with atypical Usher syndrome, but the diagnosis was adjusted in case of double homozygosity for mutations in OTOA and NR2E3, genes implicated in isolated deafness and RP. Two patients with additional enamel dysplasia had biallelic PEX26 mutations, for the first time linking this gene to Heimler syndrome. ConclusionTargeted NGS not restricted to Usher genes proved beneficial in uncovering conditions mimicking Usher syndrome.
| Item Type: | Article |
|---|---|
| Uncontrolled Keywords: | SYNDROME TYPE IIA; SYNDROME TYPE-I; PEROXISOME-BIOGENESIS DISORDERS; RECESSIVE RETINITIS-PIGMENTOSA; GENOTYPE-PHENOTYPE CORRELATION; INHERITED RETINAL DYSTROPHY; ADULT REFSUM-DISEASE; MYOSIN VIIA GENE; S-CONE-SYNDROME; USH2A GENE; Copy number variation; Heimler syndrome; next-generation sequencing; phenocopies; translational read-through; Usher syndrome |
| Subjects: | 600 Technology > 610 Medical sciences Medicine |
| Divisions: | Medicine > Lehrstuhl für Humangenetik |
| Depositing User: | Dr. Gernot Deinzer |
| Date Deposited: | 14 Dec 2018 13:15 |
| Last Modified: | 12 Feb 2019 14:56 |
| URI: | https://pred.uni-regensburg.de/id/eprint/1240 |
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