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Exome sequencing id...
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Götz, AlexandraResearch Programs Unit, Biomedicum-Helsinki, University of Helsinki, Helsinki, Finland
(författare)
Exome sequencing identifies mitochondrial alanyl-tRNA synthetase mutations in infantile mitochondrial cardiomyopathy
- Artikel/kapitelEngelska2011
Förlag, utgivningsår, omfång ...
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Cell Press,2011
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printrdacarrier
Nummerbeteckningar
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LIBRIS-ID:oai:DiVA.org:oru-63649
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https://urn.kb.se/resolve?urn=urn:nbn:se:oru:diva-63649URI
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https://doi.org/10.1016/j.ajhg.2011.04.006DOI
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Språk:engelska
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Sammanfattning på:engelska
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Ämneskategori:ref swepub-contenttype
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Ämneskategori:art swepub-publicationtype
Anmärkningar
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Funding agencies:Jane and Aatos Erkko FoundationSigrid Juselius FoundationUniversity of HelsinkiGraduate School of Biotechnology and Molecular BiologyFinnish Cultural Foundation
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Infantile cardiomyopathies are devastating fatal disorders of the neonatal period or the first year of life. Mitochondrial dysfunction is a common cause of this group of diseases, but the underlying gene defects have been characterized in only a minority of cases, because tissue specificity of the manifestation hampers functional cloning and the heterogeneity of causative factors hinders collection of informative family materials. We sequenced the exome of a patient who died at the age of 10 months of hypertrophic mitochondrial cardiomyopathy with combined cardiac respiratory chain complex I and IV deficiency. Rigorous data analysis allowed us to identify a homozygous missense mutation in AARS2, which we showed to encode the mitochondrial alanyl-tRNA synthetase (mtAlaRS). Two siblings from another family, both of whom died perinatally of hypertrophic cardiomyopathy, had the same mutation, compound heterozygous with another missense mutation. Protein structure modeling of mtAlaRS suggested that one of the mutations affected a unique tRNA recognition site in the editing domain, leading to incorrect tRNA aminoacylation, whereas the second mutation severely disturbed the catalytic function, preventing tRNA aminoacylation. We show here that mutations in AARS2 cause perinatal or infantile cardiomyopathy with near-total combined mitochondrial respiratory chain deficiency in the heart. Our results indicate that exome sequencing is a powerful tool for identifying mutations in single patients and allows recognition of the genetic background in single-gene disorders of variable clinical manifestation and tissue-specific disease. Furthermore, we show that mitochondrial disorders extend to prenatal life and are an important cause of early infantile cardiac failure.
Ämnesord och genrebeteckningar
Biuppslag (personer, institutioner, konferenser, titlar ...)
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Tyynismaa, HennaResearch Programs Unit, Biomedicum-Helsinki, University of Helsinki, Helsinki, Finland
(författare)
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Euro, LiliyaResearch Programs Unit, Biomedicum-Helsinki, University of Helsinki, Helsinki, Finland
(författare)
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Ellonen, PekkaInstitute for Molecular Medicine Finland (FIMM), University of Helsinki, Helsinki, Finland
(författare)
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Hyötyläinen, Tuulia,1971-VTT Technical Research Centre of Finland, Espoo, Finland(Swepub:oru)tihn
(författare)
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Ojala, TiinaDepartment of Pediatric Cardiology, Hospital for Children and Adolescents, University of Helsinki, Helsinki, Finland
(författare)
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Hämäläinen, Riikka HResearch Programs Unit, Biomedicum-Helsinki, University of Helsinki, Helsinki, Finland
(författare)
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Tommiska, JohannaInstitute of Biomedicine, Department of Physiology, University of Helsinki, Helsinki, Finland; Children's Hospital, Helsinki University Central Hospital, Helsinki, Finland g
(författare)
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Raivio, TaneliInstitute of Biomedicine, Department of Physiology, University of Helsinki, Helsinki, Finland; Children's Hospital, Helsinki University Central Hospital, Helsinki, Finland
(författare)
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Oresic, Matej,1967-Örebro universitet,Institutionen för medicinska vetenskaper,VTT Technical Research Centre of Finland, Espoo, Finland(Swepub:oru)moc
(författare)
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Karikoski, RiittaDepartment of Pathology, University of Helsinki, Helsinki, Finland; Helsinki University Central Hospital, Helsinki, Finland
(författare)
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Tammela, OutiPediatric Research Centre, Tampere University Hospital, Tampere, Finland
(författare)
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Simola, Kalle O JGenetics Outpatient Clinic, Department of Pediatrics, Tampere University Hospital, Tampere, Finland
(författare)
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Paetau, AndersDepartment of Pathology, University of Helsinki, Helsinki, Finland; Helsinki University Central Hospital, Helsinki, Finland
(författare)
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Tyni, TiinaResearch Programs Unit, Biomedicum-Helsinki, University of Helsinki, Helsinki, Finland; Department of Pediatric Neurology, Helsinki University Central Hospital, Helsinki, Finland
(författare)
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Suomalainen, AnuResearch Programs Unit, Biomedicum-Helsinki, University of Helsinki, Helsinki, Finland; Institute for Molecular Medicine Finland (FIMM), University of Helsinki, Helsinki, Finland; Department of Neurology, Helsinki University Central Hospital, Helsinki, Finland
(författare)
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Research Programs Unit, Biomedicum-Helsinki, University of Helsinki, Helsinki, FinlandInstitute for Molecular Medicine Finland (FIMM), University of Helsinki, Helsinki, Finland
(creator_code:org_t)
Sammanhörande titlar
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Ingår i:American Journal of Human Genetics: Cell Press88:5, s. 635-6420002-92971537-6605
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Till lärosätets databas
- Av författaren/redakt...
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Götz, Alexandra
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Tyynismaa, Henna
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Euro, Liliya
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Ellonen, Pekka
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Hyötyläinen, Tuu ...
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Ojala, Tiina
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visa fler...
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Hämäläinen, Riik ...
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Tommiska, Johann ...
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Raivio, Taneli
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Oresic, Matej, 1 ...
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Karikoski, Riitt ...
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Tammela, Outi
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Simola, Kalle O ...
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Paetau, Anders
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Tyni, Tiina
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Suomalainen, Anu
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Örebro universitet