Mutations in the mitochondrial tRNA Ser(AGY) gene are associated with deafness, retinal degeneration, myopathy and epilepsy

Helen A L Tuppen, Karin Naess, Nancy G. Kennaway, Mazhor Al-Dosary, Nicole Lesko, John W. Yarham, Helene Bruhn, Rolf Wibom, Inger Nennesmo, Richard Weleber, Emma L. Blakely, Robert W. Taylor, Robert McFarland

Research output: Contribution to journalArticle

6 Citations (Scopus)

Abstract

Although over 200 pathogenic mitochondrial DNA (mtDNA) mutations have been reported to date, determining the genetic aetiology of many cases of mitochondrial disease is still not straightforward. Here, we describe the investigations undertaken to uncover the underlying molecular defect(s) in two unrelated Caucasian patients with suspected mtDNA disease, who presented with similar symptoms of myopathy, deafness, neurodevelopmental delay, epilepsy, marked fatigue and, in one case, retinal degeneration. Histochemical and biochemical evidence of mitochondrial respiratory chain deficiency was observed in the patient muscle biopsies and both patients were discovered to harbour a novel heteroplasmic mitochondrial tRNA (mt-tRNA)Ser(AGY) (MTTS2) mutation (m.12264C>T and m.12261T>C, respectively). Clear segregation of the m.12261T>C mutation with the biochemical defect, as demonstrated by single-fibre radioactive RFLP, confirmed the pathogenicity of this novel variant in patient 2. However, unusually high levels of m.12264CT mutation within both COX-positive (98.4 ± 1.5%) and COX-deficient (98.2 ± 2.1%) fibres in patient 1 necessitated further functional investigations to prove its pathogenicity. Northern blot analysis demonstrated the detrimental effect of the m.12264C>T mutation on mt-tRNASer(AGY) stability, ultimately resulting in decreased steady-state levels of fully assembled complexes I and IV, as shown by blue-native polyacrylamide gel electrophoresis. Our findings expand the spectrum of pathogenic mutations associated with the MTTS2 gene and highlight MTTS2 mutations as an important cause of retinal and syndromic auditory impairment.

Original languageEnglish (US)
Pages (from-to)897-904
Number of pages8
JournalEuropean Journal of Human Genetics
Volume20
Issue number8
DOIs
StatePublished - Aug 2012

Fingerprint

RNA, Transfer, Ser
Deafness
Muscular Diseases
Mutation
Mitochondrial Diseases
Genes
Mitochondrial DNA
Virulence
Native Polyacrylamide Gel Electrophoresis
Retinal Degeneration
Retinal Degeneration and Epilepsy
Restriction Fragment Length Polymorphisms
Northern Blotting
Fatigue
Epilepsy
Biopsy
Muscles

Keywords

  • deafness
  • mt-tRNA
  • mutation
  • retinitis pigmentosa

ASJC Scopus subject areas

  • Genetics(clinical)
  • Genetics

Cite this

Tuppen, H. A. L., Naess, K., Kennaway, N. G., Al-Dosary, M., Lesko, N., Yarham, J. W., ... McFarland, R. (2012). Mutations in the mitochondrial tRNA Ser(AGY) gene are associated with deafness, retinal degeneration, myopathy and epilepsy. European Journal of Human Genetics, 20(8), 897-904. https://doi.org/10.1038/ejhg.2012.44

Mutations in the mitochondrial tRNA Ser(AGY) gene are associated with deafness, retinal degeneration, myopathy and epilepsy. / Tuppen, Helen A L; Naess, Karin; Kennaway, Nancy G.; Al-Dosary, Mazhor; Lesko, Nicole; Yarham, John W.; Bruhn, Helene; Wibom, Rolf; Nennesmo, Inger; Weleber, Richard; Blakely, Emma L.; Taylor, Robert W.; McFarland, Robert.

In: European Journal of Human Genetics, Vol. 20, No. 8, 08.2012, p. 897-904.

Research output: Contribution to journalArticle

Tuppen, HAL, Naess, K, Kennaway, NG, Al-Dosary, M, Lesko, N, Yarham, JW, Bruhn, H, Wibom, R, Nennesmo, I, Weleber, R, Blakely, EL, Taylor, RW & McFarland, R 2012, 'Mutations in the mitochondrial tRNA Ser(AGY) gene are associated with deafness, retinal degeneration, myopathy and epilepsy', European Journal of Human Genetics, vol. 20, no. 8, pp. 897-904. https://doi.org/10.1038/ejhg.2012.44
Tuppen, Helen A L ; Naess, Karin ; Kennaway, Nancy G. ; Al-Dosary, Mazhor ; Lesko, Nicole ; Yarham, John W. ; Bruhn, Helene ; Wibom, Rolf ; Nennesmo, Inger ; Weleber, Richard ; Blakely, Emma L. ; Taylor, Robert W. ; McFarland, Robert. / Mutations in the mitochondrial tRNA Ser(AGY) gene are associated with deafness, retinal degeneration, myopathy and epilepsy. In: European Journal of Human Genetics. 2012 ; Vol. 20, No. 8. pp. 897-904.
@article{0c9d74c108424428b8c3c2443d933b94,
title = "Mutations in the mitochondrial tRNA Ser(AGY) gene are associated with deafness, retinal degeneration, myopathy and epilepsy",
abstract = "Although over 200 pathogenic mitochondrial DNA (mtDNA) mutations have been reported to date, determining the genetic aetiology of many cases of mitochondrial disease is still not straightforward. Here, we describe the investigations undertaken to uncover the underlying molecular defect(s) in two unrelated Caucasian patients with suspected mtDNA disease, who presented with similar symptoms of myopathy, deafness, neurodevelopmental delay, epilepsy, marked fatigue and, in one case, retinal degeneration. Histochemical and biochemical evidence of mitochondrial respiratory chain deficiency was observed in the patient muscle biopsies and both patients were discovered to harbour a novel heteroplasmic mitochondrial tRNA (mt-tRNA)Ser(AGY) (MTTS2) mutation (m.12264C>T and m.12261T>C, respectively). Clear segregation of the m.12261T>C mutation with the biochemical defect, as demonstrated by single-fibre radioactive RFLP, confirmed the pathogenicity of this novel variant in patient 2. However, unusually high levels of m.12264CT mutation within both COX-positive (98.4 ± 1.5{\%}) and COX-deficient (98.2 ± 2.1{\%}) fibres in patient 1 necessitated further functional investigations to prove its pathogenicity. Northern blot analysis demonstrated the detrimental effect of the m.12264C>T mutation on mt-tRNASer(AGY) stability, ultimately resulting in decreased steady-state levels of fully assembled complexes I and IV, as shown by blue-native polyacrylamide gel electrophoresis. Our findings expand the spectrum of pathogenic mutations associated with the MTTS2 gene and highlight MTTS2 mutations as an important cause of retinal and syndromic auditory impairment.",
keywords = "deafness, mt-tRNA, mutation, retinitis pigmentosa",
author = "Tuppen, {Helen A L} and Karin Naess and Kennaway, {Nancy G.} and Mazhor Al-Dosary and Nicole Lesko and Yarham, {John W.} and Helene Bruhn and Rolf Wibom and Inger Nennesmo and Richard Weleber and Blakely, {Emma L.} and Taylor, {Robert W.} and Robert McFarland",
year = "2012",
month = "8",
doi = "10.1038/ejhg.2012.44",
language = "English (US)",
volume = "20",
pages = "897--904",
journal = "European Journal of Human Genetics",
issn = "1018-4813",
publisher = "Nature Publishing Group",
number = "8",

}

TY - JOUR

T1 - Mutations in the mitochondrial tRNA Ser(AGY) gene are associated with deafness, retinal degeneration, myopathy and epilepsy

AU - Tuppen, Helen A L

AU - Naess, Karin

AU - Kennaway, Nancy G.

AU - Al-Dosary, Mazhor

AU - Lesko, Nicole

AU - Yarham, John W.

AU - Bruhn, Helene

AU - Wibom, Rolf

AU - Nennesmo, Inger

AU - Weleber, Richard

AU - Blakely, Emma L.

AU - Taylor, Robert W.

AU - McFarland, Robert

PY - 2012/8

Y1 - 2012/8

N2 - Although over 200 pathogenic mitochondrial DNA (mtDNA) mutations have been reported to date, determining the genetic aetiology of many cases of mitochondrial disease is still not straightforward. Here, we describe the investigations undertaken to uncover the underlying molecular defect(s) in two unrelated Caucasian patients with suspected mtDNA disease, who presented with similar symptoms of myopathy, deafness, neurodevelopmental delay, epilepsy, marked fatigue and, in one case, retinal degeneration. Histochemical and biochemical evidence of mitochondrial respiratory chain deficiency was observed in the patient muscle biopsies and both patients were discovered to harbour a novel heteroplasmic mitochondrial tRNA (mt-tRNA)Ser(AGY) (MTTS2) mutation (m.12264C>T and m.12261T>C, respectively). Clear segregation of the m.12261T>C mutation with the biochemical defect, as demonstrated by single-fibre radioactive RFLP, confirmed the pathogenicity of this novel variant in patient 2. However, unusually high levels of m.12264CT mutation within both COX-positive (98.4 ± 1.5%) and COX-deficient (98.2 ± 2.1%) fibres in patient 1 necessitated further functional investigations to prove its pathogenicity. Northern blot analysis demonstrated the detrimental effect of the m.12264C>T mutation on mt-tRNASer(AGY) stability, ultimately resulting in decreased steady-state levels of fully assembled complexes I and IV, as shown by blue-native polyacrylamide gel electrophoresis. Our findings expand the spectrum of pathogenic mutations associated with the MTTS2 gene and highlight MTTS2 mutations as an important cause of retinal and syndromic auditory impairment.

AB - Although over 200 pathogenic mitochondrial DNA (mtDNA) mutations have been reported to date, determining the genetic aetiology of many cases of mitochondrial disease is still not straightforward. Here, we describe the investigations undertaken to uncover the underlying molecular defect(s) in two unrelated Caucasian patients with suspected mtDNA disease, who presented with similar symptoms of myopathy, deafness, neurodevelopmental delay, epilepsy, marked fatigue and, in one case, retinal degeneration. Histochemical and biochemical evidence of mitochondrial respiratory chain deficiency was observed in the patient muscle biopsies and both patients were discovered to harbour a novel heteroplasmic mitochondrial tRNA (mt-tRNA)Ser(AGY) (MTTS2) mutation (m.12264C>T and m.12261T>C, respectively). Clear segregation of the m.12261T>C mutation with the biochemical defect, as demonstrated by single-fibre radioactive RFLP, confirmed the pathogenicity of this novel variant in patient 2. However, unusually high levels of m.12264CT mutation within both COX-positive (98.4 ± 1.5%) and COX-deficient (98.2 ± 2.1%) fibres in patient 1 necessitated further functional investigations to prove its pathogenicity. Northern blot analysis demonstrated the detrimental effect of the m.12264C>T mutation on mt-tRNASer(AGY) stability, ultimately resulting in decreased steady-state levels of fully assembled complexes I and IV, as shown by blue-native polyacrylamide gel electrophoresis. Our findings expand the spectrum of pathogenic mutations associated with the MTTS2 gene and highlight MTTS2 mutations as an important cause of retinal and syndromic auditory impairment.

KW - deafness

KW - mt-tRNA

KW - mutation

KW - retinitis pigmentosa

UR - http://www.scopus.com/inward/record.url?scp=84864142018&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=84864142018&partnerID=8YFLogxK

U2 - 10.1038/ejhg.2012.44

DO - 10.1038/ejhg.2012.44

M3 - Article

C2 - 22378285

AN - SCOPUS:84864142018

VL - 20

SP - 897

EP - 904

JO - European Journal of Human Genetics

JF - European Journal of Human Genetics

SN - 1018-4813

IS - 8

ER -