Mutations of human NARS2, encoding the mitochondrial asparaginyl-tRNA synthetase, cause nonsyndromic deafness and Leigh syndrome.
Here we demonstrate association of variants in the mitochondrial asparaginyl-tRNA synthetase NARS2 with human hearing loss and Leigh syndrome. A homozygous missense mutation ([c.637G>T; p.Val213Phe]) is the underlying cause of nonsyndromic hearing loss (DFNB94) and compound heterozygous mutations...
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2015-03-01
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doaj-85a622f2d8104bbe96b80ab1bc1bbc102020-11-25T01:04:30ZengPublic Library of Science (PLoS)PLoS Genetics1553-73901553-74042015-03-01113e100509710.1371/journal.pgen.1005097Mutations of human NARS2, encoding the mitochondrial asparaginyl-tRNA synthetase, cause nonsyndromic deafness and Leigh syndrome.Mariella SimonElodie M RichardXinjian WangMohsin ShahzadVincent H HuangTanveer A QaiserPrasanth PotluriSarah E MahlAntonio DavilaSabiha NazliSaege HancockMargret YuJay GargusRichard ChangNada Al-SheqaihWilliam G NewmanJose AbdenurArnold StarrRashmi HegdeThomas DornAnke BuschEddie ParkJie WuHagen SchwenzerAdrian FlierlCatherine FlorentzMarie SisslerShaheen N KhanRonghua LiMin-Xin GuanThomas B FriedmanDoris K WuVincent ProcaccioSheikh RiazuddinDouglas C WallaceZubair M AhmedTaosheng HuangSaima RiazuddinHere we demonstrate association of variants in the mitochondrial asparaginyl-tRNA synthetase NARS2 with human hearing loss and Leigh syndrome. A homozygous missense mutation ([c.637G>T; p.Val213Phe]) is the underlying cause of nonsyndromic hearing loss (DFNB94) and compound heterozygous mutations ([c.969T>A; p.Tyr323*] + [c.1142A>G; p.Asn381Ser]) result in mitochondrial respiratory chain deficiency and Leigh syndrome, which is a neurodegenerative disease characterized by symmetric, bilateral lesions in the basal ganglia, thalamus, and brain stem. The severity of the genetic lesions and their effects on NARS2 protein structure cosegregate with the phenotype. A hypothetical truncated NARS2 protein, secondary to the Leigh syndrome mutation p.Tyr323* is not detectable and p.Asn381Ser further decreases NARS2 protein levels in patient fibroblasts. p.Asn381Ser also disrupts dimerization of NARS2, while the hearing loss p.Val213Phe variant has no effect on NARS2 oligomerization. Additionally we demonstrate decreased steady-state levels of mt-tRNAAsn in fibroblasts from the Leigh syndrome patients. In these cells we show that a decrease in oxygen consumption rates (OCR) and electron transport chain (ETC) activity can be rescued by overexpression of wild type NARS2. However, overexpression of the hearing loss associated p.Val213Phe mutant protein in these fibroblasts cannot complement the OCR and ETC defects. Our findings establish lesions in NARS2 as a new cause for nonsyndromic hearing loss and Leigh syndrome.http://europepmc.org/articles/PMC4373692?pdf=render |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Mariella Simon Elodie M Richard Xinjian Wang Mohsin Shahzad Vincent H Huang Tanveer A Qaiser Prasanth Potluri Sarah E Mahl Antonio Davila Sabiha Nazli Saege Hancock Margret Yu Jay Gargus Richard Chang Nada Al-Sheqaih William G Newman Jose Abdenur Arnold Starr Rashmi Hegde Thomas Dorn Anke Busch Eddie Park Jie Wu Hagen Schwenzer Adrian Flierl Catherine Florentz Marie Sissler Shaheen N Khan Ronghua Li Min-Xin Guan Thomas B Friedman Doris K Wu Vincent Procaccio Sheikh Riazuddin Douglas C Wallace Zubair M Ahmed Taosheng Huang Saima Riazuddin |
spellingShingle |
Mariella Simon Elodie M Richard Xinjian Wang Mohsin Shahzad Vincent H Huang Tanveer A Qaiser Prasanth Potluri Sarah E Mahl Antonio Davila Sabiha Nazli Saege Hancock Margret Yu Jay Gargus Richard Chang Nada Al-Sheqaih William G Newman Jose Abdenur Arnold Starr Rashmi Hegde Thomas Dorn Anke Busch Eddie Park Jie Wu Hagen Schwenzer Adrian Flierl Catherine Florentz Marie Sissler Shaheen N Khan Ronghua Li Min-Xin Guan Thomas B Friedman Doris K Wu Vincent Procaccio Sheikh Riazuddin Douglas C Wallace Zubair M Ahmed Taosheng Huang Saima Riazuddin Mutations of human NARS2, encoding the mitochondrial asparaginyl-tRNA synthetase, cause nonsyndromic deafness and Leigh syndrome. PLoS Genetics |
author_facet |
Mariella Simon Elodie M Richard Xinjian Wang Mohsin Shahzad Vincent H Huang Tanveer A Qaiser Prasanth Potluri Sarah E Mahl Antonio Davila Sabiha Nazli Saege Hancock Margret Yu Jay Gargus Richard Chang Nada Al-Sheqaih William G Newman Jose Abdenur Arnold Starr Rashmi Hegde Thomas Dorn Anke Busch Eddie Park Jie Wu Hagen Schwenzer Adrian Flierl Catherine Florentz Marie Sissler Shaheen N Khan Ronghua Li Min-Xin Guan Thomas B Friedman Doris K Wu Vincent Procaccio Sheikh Riazuddin Douglas C Wallace Zubair M Ahmed Taosheng Huang Saima Riazuddin |
author_sort |
Mariella Simon |
title |
Mutations of human NARS2, encoding the mitochondrial asparaginyl-tRNA synthetase, cause nonsyndromic deafness and Leigh syndrome. |
title_short |
Mutations of human NARS2, encoding the mitochondrial asparaginyl-tRNA synthetase, cause nonsyndromic deafness and Leigh syndrome. |
title_full |
Mutations of human NARS2, encoding the mitochondrial asparaginyl-tRNA synthetase, cause nonsyndromic deafness and Leigh syndrome. |
title_fullStr |
Mutations of human NARS2, encoding the mitochondrial asparaginyl-tRNA synthetase, cause nonsyndromic deafness and Leigh syndrome. |
title_full_unstemmed |
Mutations of human NARS2, encoding the mitochondrial asparaginyl-tRNA synthetase, cause nonsyndromic deafness and Leigh syndrome. |
title_sort |
mutations of human nars2, encoding the mitochondrial asparaginyl-trna synthetase, cause nonsyndromic deafness and leigh syndrome. |
publisher |
Public Library of Science (PLoS) |
series |
PLoS Genetics |
issn |
1553-7390 1553-7404 |
publishDate |
2015-03-01 |
description |
Here we demonstrate association of variants in the mitochondrial asparaginyl-tRNA synthetase NARS2 with human hearing loss and Leigh syndrome. A homozygous missense mutation ([c.637G>T; p.Val213Phe]) is the underlying cause of nonsyndromic hearing loss (DFNB94) and compound heterozygous mutations ([c.969T>A; p.Tyr323*] + [c.1142A>G; p.Asn381Ser]) result in mitochondrial respiratory chain deficiency and Leigh syndrome, which is a neurodegenerative disease characterized by symmetric, bilateral lesions in the basal ganglia, thalamus, and brain stem. The severity of the genetic lesions and their effects on NARS2 protein structure cosegregate with the phenotype. A hypothetical truncated NARS2 protein, secondary to the Leigh syndrome mutation p.Tyr323* is not detectable and p.Asn381Ser further decreases NARS2 protein levels in patient fibroblasts. p.Asn381Ser also disrupts dimerization of NARS2, while the hearing loss p.Val213Phe variant has no effect on NARS2 oligomerization. Additionally we demonstrate decreased steady-state levels of mt-tRNAAsn in fibroblasts from the Leigh syndrome patients. In these cells we show that a decrease in oxygen consumption rates (OCR) and electron transport chain (ETC) activity can be rescued by overexpression of wild type NARS2. However, overexpression of the hearing loss associated p.Val213Phe mutant protein in these fibroblasts cannot complement the OCR and ETC defects. Our findings establish lesions in NARS2 as a new cause for nonsyndromic hearing loss and Leigh syndrome. |
url |
http://europepmc.org/articles/PMC4373692?pdf=render |
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