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Defining the pathogenesis of human mtDNA mutations using a yeast model : the case of T8851C

Kucharczyk, Roza and Giraud, Marie-France and Brèthes, Daniel and Wysocka-Kapcinska, Monika and Ezkurdia, Nahia and Salin, Bénédicte and Velours, Jean and Camougrand, Nadine and Francis Haraux, Francis and di Rago, Jean-Paul (2012) Defining the pathogenesis of human mtDNA mutations using a yeast model : the case of T8851C. The International Journal of Biochemistry & Cell Biology, 45 . pp. 130-140. ISSN 1357-2725

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Official URL: http://www.ncbi.nlm.nih.gov/pubmed/22789932


More and more mutations are found in the mitochondrial DNA of various patients but ascertaining their pathogenesis is often difficult. Due to the conservation of mitochondrial function from yeast to humans, the unique ability of yeast to survive without production of ATP by oxidative phosphorylation, and the amenability of the yeast mitochondrial genome to site-directed mutagenesis, yeast is an excellent model for investigating the consequences of specific human mtDNA mutations. Here we report the construction of a yeast model of a point mutation (T8851C) in the mitochondrially-encoded subunit a/6 of the ATP synthase that has been associated with bilateral striatal lesions, a group of rare human neurological disorders characterized by symmetric degeneration of the corpus striatum. The biochemical consequences of this mutation are unknown. The T8851C yeast displayed a very slow growth phenotype on non-fermentable carbon sources, both at 28°C (the optimal temperature for yeast growth) and at 36°C. Mitochondria from T8851C yeast grown in galactose at 28°C showed a 60% deficit in ATP production. When grown at 36°C the rate of ATP synthesis was below 5% that of the wild-type, indicating that heat renders the mutation much more deleterious. At both growth temperatures, the mutant F1FO complex was correctly assembled but had only very weak ATPase activity (about 10% that of the control), both in mitochondria and after purification. These findings indicate that a block in the proton-translocating domain of the ATP synthase is the primary cause of the neurological disorder in the patients carrying the T8851C mutation.

Item Type:Article
Subjects:Q Science > Q Science (General)
Divisions:Department of Genetics
ID Code:423
Deposited By: Dr hab Roza Kucharczyk
Deposited On:09 Jan 2013 09:29
Last Modified:01 Oct 2015 08:01

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