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Inhibition of Fe-S cluster biosynthesis decreases mitochondrial iron export: Evidence that Yfh1p affects Fe-S cluster synthesis

机译:抑制Fe-S团簇生物合成减少线粒体铁的输出:Yfh1p影响Fe-S团簇合成的证据

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摘要

Decreased expression of Yfh1p in the budding yeast, Saccharomyces cerevisiae, and the orthologous human gene frataxin results in respiratory deficiency and mitochondrial iron accumulation. The absence of Yfh1p decreases mitochondrial iron export. We demonstrate that decreased expression of Nfs1p, the yeast cysteine desulfurase that plays a central role in Fe-S cluster synthesis, also results in mitochondrial iron accumulation due to decreased export of mitochondrial iron. In the absence of Yfh1p, activity of Fe-S-containing enzymes (aconitase, succinate dehydrogenase) is decreased, whereas the activity of a non-Fe-S-containing enzyme (malate dehydrogenase) is unaffected. Aconitase protein was abundant even though the activity of aconitase was decreased in both aerobic and anaerobic conditions. These results demonstrate a direct role of Yfh1p in the formation of Fe-S clusters and indicate that mitochondrial iron export requires Fe-S cluster biosynthesis.
机译:Yfh1p在发芽酵母,酿酒酵母中的表达减少,而直系同源的人类基因frataxin导致呼吸系统缺乏和线粒体铁积累。 Yfh1p的缺乏减少了线粒体铁的出口。我们证明Nfs1p的表达下降,酵母半胱氨酸脱硫酶在Fe-S簇合成中起核心作用,由于线粒体铁的出口减少,也导致线粒体铁积累。在没有Yfh1p的情况下,含Fe-S的酶((酸酶,琥珀酸脱氢酶)的活性降低,而不含Fe-S的酶(苹果酸脱氢酶)的活性不受影响。即使在有氧和无氧条件下乌头酸酶的活性均降低,乌头酸酶的蛋白质仍然丰富。这些结果证明Yfh1p在Fe-S团簇的形成中具有直接作用,并表明线粒体铁输出需要Fe-S团簇的生物合成。

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