Saccharomyces cerevisiae ISU1 and ISU2: members of a well-conserved gene family for iron-sulfur cluster assembly.

IF 4.7 2区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Journal of Molecular Biology Pub Date : 1999-12-10 DOI:10.1006/jmbi.1999.3294
S A Garland, K Hoff, L E Vickery, V C Culotta
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引用次数: 191

Abstract

Recent studies in bacteria and eukaryotes have led to the identification of several new genes implicated in the biogenesis of iron-sulfur (Fe/S) cluster-containing proteins. This report focuses on two genes of bakers yeast Saccharomyces cerevisiae, ISU1 and ISU2, which encode homologues to bacterial IscU and NifU, potential iron-binding or cluster-assembly proteins. As with other yeast genes implicated in Fe/S protein assembly, deletion of either ISU1 or ISU2 results in increased accumulation of iron within the mitochondria, loss of activity of the [4Fe-4S] aconitase enzyme, and suppression of oxidative damage in cells lacking cytosolic copper/zinc superoxide dismutase. Both genes are induced in strains expressing an activated allele of Aft1p, the iron-sensing transcription factor, suggesting that they are regulated by the iron status of the cell. Immunoblotting studies using an antibody directed against Escherichia coli IscU reveal that both Isu1p and Isu2p are localized primarily in the mitochondria and that Isu1p is the predominant form expressed under all growth conditions tested. The possible role of the Isu proteins in the assembly and/or repair of Fe/S clusters is discussed.

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酿酒酵母ISU1和ISU2:一个保守的铁硫簇组装基因家族的成员。
最近对细菌和真核生物的研究发现了几个与含铁硫(Fe/S)簇蛋白的生物发生有关的新基因。本文重点研究了酿酒酵母ISU1和ISU2基因,这两个基因编码了细菌IscU和NifU的同源物,这两个基因是潜在的铁结合或簇组装蛋白。与其他与铁/硫蛋白组装有关的酵母基因一样,ISU1或ISU2的缺失会导致线粒体内铁积累增加,[4Fe-4S]乌头酶活性丧失,并抑制细胞内缺乏铜/锌超氧化物歧化酶的细胞的氧化损伤。这两个基因在表达铁感应转录因子Aft1p的激活等位基因的菌株中都被诱导,这表明它们受细胞铁状态的调节。使用针对大肠杆菌IscU的抗体进行免疫印迹研究表明,Isu1p和Isu2p主要定位于线粒体,Isu1p在所有生长条件下都是主要表达形式。讨论了Isu蛋白在Fe/S簇的组装和/或修复中的可能作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Molecular Biology
Journal of Molecular Biology 生物-生化与分子生物学
CiteScore
11.30
自引率
1.80%
发文量
412
审稿时长
28 days
期刊介绍: Journal of Molecular Biology (JMB) provides high quality, comprehensive and broad coverage in all areas of molecular biology. The journal publishes original scientific research papers that provide mechanistic and functional insights and report a significant advance to the field. The journal encourages the submission of multidisciplinary studies that use complementary experimental and computational approaches to address challenging biological questions. Research areas include but are not limited to: Biomolecular interactions, signaling networks, systems biology; Cell cycle, cell growth, cell differentiation; Cell death, autophagy; Cell signaling and regulation; Chemical biology; Computational biology, in combination with experimental studies; DNA replication, repair, and recombination; Development, regenerative biology, mechanistic and functional studies of stem cells; Epigenetics, chromatin structure and function; Gene expression; Membrane processes, cell surface proteins and cell-cell interactions; Methodological advances, both experimental and theoretical, including databases; Microbiology, virology, and interactions with the host or environment; Microbiota mechanistic and functional studies; Nuclear organization; Post-translational modifications, proteomics; Processing and function of biologically important macromolecules and complexes; Molecular basis of disease; RNA processing, structure and functions of non-coding RNAs, transcription; Sorting, spatiotemporal organization, trafficking; Structural biology; Synthetic biology; Translation, protein folding, chaperones, protein degradation and quality control.
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