Your browser doesn't support javascript.
loading
The effect on mitochondrial function of the tRNA Ser(UCN)/COI A7445G mtDNA point mutation associated with maternally-inherited sensorineural deafness.
Hyslop, S J; James, A M; Maw, M; Fischel-Ghodsian, N; Murphy, M P.
Afiliación
  • Hyslop SJ; Department of Biochemistry, University of Otago, Dunedin, New Zealand.
Biochem Mol Biol Int ; 42(3): 567-75, 1997 Jul.
Article en En | MEDLINE | ID: mdl-9247714
ABSTRACT
An A to G point mutation at nucleotide position 7445 in the mitochondrial DNA genome is associated with maternally-inherited sensorineural deafness in two separate human pedigrees. To determine whether this point mutation [tRNA(SER)UCN)/COI A7445G] led to sensorineural deafness by affecting cellular energy metabolism we investigated the bioenergetic function of mitochondria in lymphoblastoid cultures established from these patients. Even though essentially all of the mitochondrial DNA in these cells contained the mutation at nucleotide position 7445, there was no effect on a number of mitochondrial bioenergetic functions (mitochondrial content, membrane potential in both intact and digitonin-permeabilised cells, cellular ATP/ADP ratios and respiratory enzyme activity) when compared with control cells. The implications of these findings for both the aetiology of the sensorineural deafness associated with the A7445G mtDNA mutation, and the role of bioenergetic defects in mitochondrial DNA diseases in general are discussed.
Asunto(s)
Buscar en Google
Colección: 01-internacional Base de datos: MEDLINE Asunto principal: ADN Mitocondrial / ARN de Transferencia de Serina / Mutación Puntual / Sordera / Mitocondrias Tipo de estudio: Risk_factors_studies Límite: Female / Humans / Male Idioma: En Revista: Biochem Mol Biol Int Asunto de la revista: BIOLOGIA MOLECULAR / BIOQUIMICA Año: 1997 Tipo del documento: Article País de afiliación: Nueva Zelanda
Buscar en Google
Colección: 01-internacional Base de datos: MEDLINE Asunto principal: ADN Mitocondrial / ARN de Transferencia de Serina / Mutación Puntual / Sordera / Mitocondrias Tipo de estudio: Risk_factors_studies Límite: Female / Humans / Male Idioma: En Revista: Biochem Mol Biol Int Asunto de la revista: BIOLOGIA MOLECULAR / BIOQUIMICA Año: 1997 Tipo del documento: Article País de afiliación: Nueva Zelanda