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Metal Homeostasis Regulators Suppress FRDA Phenotypes in a Drosophila Model of the Disease.

PLoS One. 2016 Jul 19;11(7):e0159209. eCollection 2016
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摘要


Friedreich's ataxia the most commonly inherited ataxia in populations of European origin, is a neurodegenerative disorder caused by a decrease in frataxin levels. One of the hallmarks of the disease is the accumulation of iron in several tissues including the brain, and frataxin has been proposed to play a key role in iron homeostasis. We found that the levels of zinc, copper, manganese and aluminum were also increased in a Drosophila model of and that copper and zinc chelation improve their impaired motor performance. By means of a candidate genetic screen, we identified that genes implicated in iron, zinc and copper transport and metal detoxification can restore frataxin deficiency-induced phenotypes. Taken together, these results demonstrate that the metal dysregulation in includes other metals besides iron, therefore providing a new set of potential therapeutic targets.

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