Literature DB >> 16510442

Manganese is the link between frataxin and iron-sulfur deficiency in the yeast model of Friedreich ataxia.

Verónica Irazusta1, Elisa Cabiscol, Gemma Reverter-Branchat, Joaquim Ros, Jordi Tamarit.   

Abstract

Friedreich ataxia is a human neurodegenerative and myocardial disease caused by decreased expression of the mitochondrial protein frataxin. Proteomic analysis of the mutant yeast model of Friedreich ataxia presented in this paper reveals that these cells display increased amounts of proteins involved in antioxidant defenses, including manganese-superoxide dismutase. This enzyme shows, however, lower activity than that found in wild type cells. Our results indicate that this lack of activity is a consequence of cellular manganese deficiency, because in manganese-supplemented cultures, cell manganese content, and manganese-superoxide dismutase activity were restored. One of the hallmarks of Friedreich ataxia is the decreased activity of iron/sulfur-containing enzymes. The activities of four enzymes of this group (aconitase, glutamate synthase, succinate dehydrogenase, and isopropylmalate dehydratase) have been analyzed for the effects of manganese supplementation. Enzyme activities were recovered by manganese treatment, except for aconitase, for which, a specific interaction with frataxin has been demonstrated previously. Similar results were obtained when cells were grown in iron-limited media suggesting that manganese-superoxide dismutase deficiency is a consequence of iron overload. In conclusion, these data indicate that generalized deficiency of iron-sulfur protein activity could be a consequence of manganese-superoxide dismutase deficiency, and consequently, it opens new strategies for Friedreich ataxia treatment.

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Year:  2006        PMID: 16510442     DOI: 10.1074/jbc.M511649200

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  27 in total

1.  Frataxin depletion in yeast triggers up-regulation of iron transport systems before affecting iron-sulfur enzyme activities.

Authors:  Armando Moreno-Cermeño; Elia Obis; Gemma Bellí; Elisa Cabiscol; Joaquim Ros; Jordi Tamarit
Journal:  J Biol Chem       Date:  2010-10-18       Impact factor: 5.157

Review 2.  Advancements in the pathophysiology of Friedreich's Ataxia and new prospects for treatments.

Authors:  Ngolela E Babady; Nadege Carelle; Robert D Wells; Tracey A Rouault; Michio Hirano; David R Lynch; Martin B Delatycki; Robert B Wilson; Grazia Isaya; Hélène Puccio
Journal:  Mol Genet Metab       Date:  2007-06-26       Impact factor: 4.797

3.  Isc1p plays a key role in hydrogen peroxide resistance and chronological lifespan through modulation of iron levels and apoptosis.

Authors:  Teresa Almeida; Marta Marques; Dominik Mojzita; Maria A Amorim; Rui D Silva; Bruno Almeida; Pedro Rodrigues; Paula Ludovico; Stefan Hohmann; Pedro Moradas-Ferreira; Manuela Côrte-Real; Vítor Costa
Journal:  Mol Biol Cell       Date:  2007-12-27       Impact factor: 4.138

4.  Human mesenchymal stem cells increase anti-oxidant defences in cells derived from patients with Friedreich's ataxia.

Authors:  Rimi Dey; Kevin Kemp; Elizabeth Gray; Claire Rice; Neil Scolding; Alastair Wilkins
Journal:  Cerebellum       Date:  2012-12       Impact factor: 3.847

Review 5.  The structure and function of frataxin.

Authors:  Krisztina Z Bencze; Kalyan C Kondapalli; Jeremy D Cook; Stephen McMahon; César Millán-Pacheco; Nina Pastor; Timothy L Stemmler
Journal:  Crit Rev Biochem Mol Biol       Date:  2006 Sep-Oct       Impact factor: 8.250

6.  The forkhead transcription factor Hcm1 promotes mitochondrial biogenesis and stress resistance in yeast.

Authors:  Maria José Rodriguez-Colman; Gemma Reverter-Branchat; M Alba Sorolla; Jordi Tamarit; Joaquim Ros; Elisa Cabiscol
Journal:  J Biol Chem       Date:  2010-09-16       Impact factor: 5.157

7.  Blood cells from Friedreich ataxia patients harbor frataxin deficiency without a loss of mitochondrial function.

Authors:  Mary A Selak; Elise Lyver; Elizabeth Micklow; Eric C Deutsch; Ozlem Onder; Nur Selamoglu; Claire Yager; Simon Knight; Martin Carroll; Fevzi Daldal; Andrew Dancis; David R Lynch; Jean-Emmanuel Sarry
Journal:  Mitochondrion       Date:  2010-12-13       Impact factor: 4.160

8.  A SLC39A8 variant causes manganese deficiency, and glycosylation and mitochondrial disorders.

Authors:  Lisa G Riley; Mark J Cowley; Velimir Gayevskiy; Tony Roscioli; David R Thorburn; Kristina Prelog; Melanie Bahlo; Carolyn M Sue; Shanti Balasubramaniam; John Christodoulou
Journal:  J Inherit Metab Dis       Date:  2016-12-19       Impact factor: 4.982

9.  Iron-mediated inhibition of mitochondrial manganese uptake mediates mitochondrial dysfunction in a mouse model of hemochromatosis.

Authors:  Hani A Jouihan; Paul A Cobine; Robert C Cooksey; Emily A Hoagland; Sihem Boudina; E Dale Abel; Dennis R Winge; Donald A McClain
Journal:  Mol Med       Date:  2008 Mar-Apr       Impact factor: 6.354

10.  Iron behaving badly: inappropriate iron chelation as a major contributor to the aetiology of vascular and other progressive inflammatory and degenerative diseases.

Authors:  Douglas B Kell
Journal:  BMC Med Genomics       Date:  2009-01-08       Impact factor: 3.063

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