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Feichtinger, R.G.* ; Oláhová, M.* ; Kishita, Y.* ; Garone, C.* ; Kremer, L.S. ; Yagi, M.* ; Uchiumi, T.* ; Jourdain, A.A.* ; Thompson, K.* ; D'Souza, A.R.* ; Kopajtich, R.* ; Alston, C.L.* ; Koch, J.* ; Sperl, W.* ; Mastantuono, E. ; Strom, T.M. ; Wortmann, S.B. ; Meitinger, T. ; Pierre, G.* ; Chinnery, P.F.* ; Chrzanowska-Lightowlers, Z.M.* ; Lightowlers, R.N.* ; DiMauro, S.* ; Calvo, S.E.* ; Mootha, V.K.* ; Moggio, M.* ; Sciacco, M.* ; Comi, G.P.* ; Ronchi, D.* ; Murayama, K.* ; Ohtake, A.* ; Rebelo-Guiomar, P.* ; Kohda, M.* ; Kang, D.* ; Mayr, J.A.* ; Taylor, R.W.* ; Okazaki, Y.* ; Minczuk, M.* ; Prokisch, H.

Biallelic C1QBP mutations cause severe neonatal-, childhood-, or later-onset cardiomyopathy associated with combined respiratory-chain deficiencies.

Am. J. Hum. Genet. 101, 525-538 (2017)
Verlagsversion Forschungsdaten DOI PMC
Open Access Gold (Paid Option)
Creative Commons Lizenzvertrag
Complement component 1 Q subcomponent-binding protein (C1QBP; also known as p32) is a multi-compartmental protein whose precise function remains unknown. It is an evolutionary conserved multifunctional protein localized primarily in the mitochondrial matrix and has roles in inflammation and infection processes, mitochondrial ribosome biogenesis, and regulation of apoptosis and nuclear transcription. It has an N-terminal mitochondrial targeting peptide that is proteolytically processed after import into the mitochondrial matrix, where it forms a homotrimeric complex organized in a doughnut-shaped structure. Although C1QBP has been reported to exert pleiotropic effects on many cellular processes, we report here four individuals from unrelated families where biallelic mutations in C1QBP cause a defect in mitochondrial energy metabolism. Infants presented with cardiomyopathy accompanied by multisystemic involvement (liver, kidney, and brain), and children and adults presented with myopathy and progressive external ophthalmoplegia. Multiple mitochondrial respiratory-chain defects, associated with the accumulation of multiple deletions of mitochondrial DNA in the later-onset myopathic cases, were identified in all affected individuals. Steady-state C1QBP levels were decreased in all individuals' samples, leading to combined respiratory-chain enzyme deficiency of complexes I, III, and IV. C1qbp(-/-) mouse embryonic fibroblasts (MEFs) resembled the human disease phenotype by showing multiple defects in oxidative phosphorylation (OXPHOS). Complementation with wild-type, but not mutagenized, C1qbp restored OXPHOS protein levels and mitochondrial enzyme activities in C1qbp(-/-) MEFs. C1QBP deficiency represents an important mitochondrial disorder associated with a clinical spectrum ranging from infantile lactic acidosis to childhood (cardio)myopathy and late-onset progressive external ophthalmoplegia.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Schlagwörter Mam33 ; Peo ; Lactate ; Mitochondria ; Multiple Mtdna Deletions ; Myopathy ; Oxidative Phosphorylation ; P32 ; Progressive External Ophthalmoplegia; Mitochondrial-dna Deletions; Oxidative-phosphorylation; P-32 Protein; Gclq-r; Disease; Matrix; Mtdna; Maintenance; P32/gc1qr; Disorder
ISSN (print) / ISBN 0002-9297
e-ISSN 1537-6605
Zeitschrift American Journal of Human Genetics, The
Quellenangaben Band: 101, Heft: 4, Seiten: 525-538 Artikelnummer: , Supplement: ,
Verlag Elsevier
Verlagsort New York, NY