Gerber Jana, Neumann Karina, Prohl Corinna, Mühlenhoff Ulrich, Lill Roland
Institut für Zytobiologie und Zytopathologie, Philipps-Universität Marburg, Robert-Koch Strasse 6, D-35033 Marburg, Germany.
Mol Cell Biol. 2004 Jun;24(11):4848-57. doi: 10.1128/MCB.24.11.4848-4857.2004.
Iron-sulfur (Fe/S) proteins are located in mitochondria, cytosol, and nucleus. Mitochondrial Fe/S proteins are matured by the iron-sulfur cluster (ISC) assembly machinery. Little is known about the formation of Fe/S proteins in the cytosol and nucleus. A function of mitochondria in cytosolic Fe/S protein maturation has been noted, but small amounts of some ISC components have been detected outside mitochondria. Here, we studied the highly conserved yeast proteins Isu1p and Isu2p, which provide a scaffold for Fe/S cluster synthesis. We asked whether the Isu proteins are needed for biosynthesis of cytosolic Fe/S clusters and in which subcellular compartment the Isu proteins are required. The Isu proteins were found to be essential for de novo biosynthesis of both mitochondrial and cytosolic Fe/S proteins. Several lines of evidence indicate that Isu1p and Isu2p have to be located inside mitochondria in order to perform their function in cytosolic Fe/S protein maturation. We were unable to mislocalize Isu1p to the cytosol due to the presence of multiple, independent mitochondrial targeting signals in this protein. Further, the bacterial homologue IscU and the human Isu proteins (partially) complemented the defects of yeast Isu protein-depleted cells in growth rate, Fe/S protein biogenesis, and iron homeostasis, yet only after targeting to mitochondria. Together, our data suggest that the Isu proteins need to be localized in mitochondria to fulfill their functional requirement in Fe/S protein maturation in the cytosol.
铁硫(Fe/S)蛋白位于线粒体、细胞质和细胞核中。线粒体Fe/S蛋白由铁硫簇(ISC)组装机制成熟。关于细胞质和细胞核中Fe/S蛋白的形成知之甚少。已经注意到线粒体在细胞质Fe/S蛋白成熟中的作用,但在线粒体外检测到少量的一些ISC成分。在这里,我们研究了高度保守的酵母蛋白Isu1p和Isu2p,它们为Fe/S簇的合成提供了一个支架。我们询问Isu蛋白是否是细胞质Fe/S簇生物合成所必需的,以及Isu蛋白在哪个亚细胞区室中是必需的。发现Isu蛋白对于线粒体和细胞质Fe/S蛋白的从头生物合成都是必不可少的。几条证据表明,Isu1p和Isu2p必须位于线粒体内,以便在细胞质Fe/S蛋白成熟中发挥其功能。由于该蛋白中存在多个独立的线粒体靶向信号,我们无法将Isu1p错误定位到细胞质中。此外,细菌同源物IscU和人类Isu蛋白(部分)补充了酵母Isu蛋白缺失细胞在生长速率、Fe/S蛋白生物合成和铁稳态方面的缺陷,但仅在靶向线粒体后。总之,我们的数据表明,Isu蛋白需要定位于线粒体中,以满足它们在细胞质中Fe/S蛋白成熟中的功能需求。