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Article: MITF variants cause nonsyndromic sensorineural hearing loss with autosomal recessive inheritance

TitleMITF variants cause nonsyndromic sensorineural hearing loss with autosomal recessive inheritance
Authors
KeywordsNonsyndromic Deafness
Connexin 26
Hearing Impairment
Issue Date2020
PublisherNature Research (part of Springer Nature): Fully open access journals. The Journal's web site is located at http://www.nature.com/srep/index.html
Citation
Scientific Reports, 2020, v. 10, p. article no. 12712 How to Cite?
AbstractMITF is a known gene underlying autosomal dominant hearing loss, Waardenburg syndrome (WS). Biallelic MITF mutations have been found associated with a rare hearing loss syndrome consisting eye abnormalities and albinism; and a more severe type of WS whose heterozygous parents were affected with classic WS in both cases. The aims of this study were to identify a new candidate gene causing autosomal recessive nonsyndromic hearing loss (ARNSHL) and confirm its causation by finding additional families affected with the candidate gene and supporting evidences from functional analyses. By using whole exome sequencing, we identified a homozygous c.1022G>A: p.Arg341His variant of MITF, which co-segregated with the hearing loss in five affected children of a consanguineous hearing couple. Targeted exome sequencing in a cohort of 130 NSHL individuals, using our in-house gene panel revealed a second family with c.1021C>T: p.Arg341Cys MITF variant. Functional studies confirmed that the Arg341His and Arg341Cys alleles yielded a normal sized MITF protein, with aberrant cytosolic localization as supported by the molecular model and the reporter assay. In conclusion, we demonstrate MITF as a new cause of ARNSHL, with heterozygous individuals free of symptoms. MITF should be included in clinical testing for NSHL, though it is rare.
Persistent Identifierhttp://hdl.handle.net/10722/285433
ISSN
2023 Impact Factor: 3.8
2023 SCImago Journal Rankings: 0.900
PubMed Central ID
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorThongpradit, S-
dc.contributor.authorJinawath, N-
dc.contributor.authorJaved, A-
dc.contributor.authorNoojarern, S-
dc.contributor.authorKhongkraparn, A-
dc.contributor.authorTim-Aroon, T-
dc.contributor.authorLertsukprasert, K-
dc.contributor.authorSuktitipat, B-
dc.contributor.authorJensen, L-
dc.contributor.authorWattanasirichaigoon, D-
dc.date.accessioned2020-08-18T03:53:22Z-
dc.date.available2020-08-18T03:53:22Z-
dc.date.issued2020-
dc.identifier.citationScientific Reports, 2020, v. 10, p. article no. 12712-
dc.identifier.issn2045-2322-
dc.identifier.urihttp://hdl.handle.net/10722/285433-
dc.description.abstractMITF is a known gene underlying autosomal dominant hearing loss, Waardenburg syndrome (WS). Biallelic MITF mutations have been found associated with a rare hearing loss syndrome consisting eye abnormalities and albinism; and a more severe type of WS whose heterozygous parents were affected with classic WS in both cases. The aims of this study were to identify a new candidate gene causing autosomal recessive nonsyndromic hearing loss (ARNSHL) and confirm its causation by finding additional families affected with the candidate gene and supporting evidences from functional analyses. By using whole exome sequencing, we identified a homozygous c.1022G>A: p.Arg341His variant of MITF, which co-segregated with the hearing loss in five affected children of a consanguineous hearing couple. Targeted exome sequencing in a cohort of 130 NSHL individuals, using our in-house gene panel revealed a second family with c.1021C>T: p.Arg341Cys MITF variant. Functional studies confirmed that the Arg341His and Arg341Cys alleles yielded a normal sized MITF protein, with aberrant cytosolic localization as supported by the molecular model and the reporter assay. In conclusion, we demonstrate MITF as a new cause of ARNSHL, with heterozygous individuals free of symptoms. MITF should be included in clinical testing for NSHL, though it is rare.-
dc.languageeng-
dc.publisherNature Research (part of Springer Nature): Fully open access journals. The Journal's web site is located at http://www.nature.com/srep/index.html-
dc.relation.ispartofScientific Reports-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectNonsyndromic Deafness-
dc.subjectConnexin 26-
dc.subjectHearing Impairment-
dc.titleMITF variants cause nonsyndromic sensorineural hearing loss with autosomal recessive inheritance-
dc.typeArticle-
dc.identifier.emailJaved, A: javed@hku.hk-
dc.identifier.authorityJaved, A=rp02386-
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.1038/s41598-020-69633-4-
dc.identifier.pmid32728090-
dc.identifier.pmcidPMC7391749-
dc.identifier.scopuseid_2-s2.0-85088705167-
dc.identifier.hkuros312832-
dc.identifier.volume10-
dc.identifier.spagearticle no. 12712-
dc.identifier.epagearticle no. 12712-
dc.identifier.isiWOS:000556385700025-
dc.publisher.placeUnited Kingdom-
dc.identifier.issnl2045-2322-

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