Clinical, Molecular, and Computational Analysis in two cases with mitochondrial encephalomyopathy associated with SUCLG1 mutation in a consanguineous family.

Autor: Maalej M; Laboratory of Molecular and Functional Genetics, Faculty of Science of Sfax, University of Sfax, Tunisia; Laboratory of Human Molecular Genetics, Faculty of Medicine of Sfax, University of Sfax, Tunisia. Electronic address: marwamaalej7@gmail.com., Tej A; Service de pédiatrie, C.H.U. Farhat Hachad de sousse, University of Sousse, Tunisia., Bouguila J; Service de pédiatrie, C.H.U. Farhat Hachad de sousse, University of Sousse, Tunisia., Tilouche S; Service de pédiatrie, C.H.U. Farhat Hachad de sousse, University of Sousse, Tunisia., Majdoub S; Service de Radiologie, CHU Farhat Hached, Sousse, University of Sousse, Tunisia., Khabou B; Laboratory of Human Molecular Genetics, Faculty of Medicine of Sfax, University of Sfax, Tunisia., Tabbebi M; Laboratory of Human Molecular Genetics, Faculty of Medicine of Sfax, University of Sfax, Tunisia., Felhi R; Laboratory of Molecular and Functional Genetics, Faculty of Science of Sfax, University of Sfax, Tunisia., Ammar M; Laboratory of Molecular and Functional Genetics, Faculty of Science of Sfax, University of Sfax, Tunisia., Mkaouar-Rebai E; Laboratory of Molecular and Functional Genetics, Faculty of Science of Sfax, University of Sfax, Tunisia., Keskes L; Laboratory of Human Molecular Genetics, Faculty of Medicine of Sfax, University of Sfax, Tunisia., Boughamoura L; Service de pédiatrie, C.H.U. Farhat Hachad de sousse, University of Sousse, Tunisia., Fakhfakh F; Laboratory of Molecular and Functional Genetics, Faculty of Science of Sfax, University of Sfax, Tunisia. Electronic address: faiza.fakhfakh02@gmail.com.
Jazyk: angličtina
Zdroj: Biochemical and biophysical research communications [Biochem Biophys Res Commun] 2018 Jan 08; Vol. 495 (2), pp. 1730-1737. Date of Electronic Publication: 2017 Dec 05.
DOI: 10.1016/j.bbrc.2017.12.011
Abstrakt: Deficiency of the mitochondrial enzyme succinyl COA ligase (SUCL) is associated with encephalomyopathic mtDNA depletion syndrome and methylmalonic aciduria. This disorder is caused by mutations in both SUCL subunits genes: SUCLG1 (α subnit) and SUCLA2 (β subnit). We report here, two Tunisian patients belonging to a consanguineous family with mitochondrial encephalomyopathy, hearing loss, lactic acidosis, hypotonia, psychomotor retardation and methylmalonic aciduria. Mutational analysis of SUCLG1 gene showed, for the first time, the presence of c.41T > C in the exon 1 at homozygous state. In-silico analysis revealed that this mutation substitutes a conserved methionine residue to a threonine at position 14 (p.M14T) located at the SUCLG1 protein mitochondrial targeting sequence. Moreover, these analysis predicted that this mutation alter stability structure and mitochondrial translocation of the protein. In Addition, a decrease in mtDNA copy number was revealed by real time PCR in the peripheral blood leukocytes in the two patients compared with controls.
(Copyright © 2017 Elsevier Inc. All rights reserved.)
Databáze: MEDLINE
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