Evidence that yeast frataxin is not an iron storage protein in vivo
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- 作者：Alex ; ra Seguin ; Robert Sutak ; Anne-Laure Bulteau ; Richard Garcia-Serres ; Jean-Louis Oddou ; Sophie Lefevre ; Renata Santos ; Andrew Dancis ; Jean-Michel Camadro ; Jean-Marc Latour ; Emmanuel Lesuisse
- 关键词：Yeast frataxin ; Iron ; Oxidative stress ; yfh1 ; ggc1 ; Mö ; ssbauer ; Mitochondrion
- 刊名：Biochimica et Biophysica Acta (BBA)/Molecular Basis of Disease
- 出版年：2010
- 出版时间：June 2010
- 年：2010
- 卷：1802
- 期：6
- 页码：531-538
- 全文大小：666 K
文摘
Yeast cells deficient in the yeast frataxin homolog (Yfh1p) accumulate iron in their mitochondria. Whether this iron is toxic, however, remains unclear. We showed that large excesses of iron in the growth medium did not inhibit growth and did not decrease cell viability. Increasing the ratio of mitochondrial iron-to-Yfh1p by decreasing the steady-state level of Yfh1p to less than 100 molecules per cell had very few deleterious effects on cell physiology, even though the mitochondrial iron concentration greatly exceeded the iron-binding capacity of Yfh1p in these conditions. Mössbauer spectroscopy and FPLC analyses of whole mitochondria or of isolated mitochondrial matrices showed that the chemical and biochemical forms of the accumulated iron in mitochondria of mutant yeast strains (Δyfh1, Δggc1 and Δssq1) displayed a nearly identical distribution. This was also the case for Δggc1 cells, in which Yfh1p was overproduced. In these mitochondria, most of the iron was insoluble, and the ratio of soluble-to-insoluble iron did not change when the amount of Yfh1p was increased up to 4500 molecules per cell. Our results do not privilege the hypothesis of Yfh1p being an iron storage protein in vivo.