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

被引:162
作者
Garland, SA
Hoff, K
Vickery, LE
Culotta, VC [1 ]
机构
[1] Johns Hopkins Univ, Sch Publ Hlth, Dept Biochem & Mol Biol, Baltimore, MD 21205 USA
[2] Johns Hopkins Univ, Sch Publ Hlth, Dept Environm Hlth Sci, Baltimore, MD 21205 USA
[3] Univ Calif Irvine, Dept Physiol & Biophys, Irvine, CA 92697 USA
关键词
iron; superoxide; yeast; ISU; iscU;
D O I
10.1006/jmbi.1999.3294
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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. (C) 1999 Academic Press.
引用
收藏
页码:897 / 907
页数:11
相关论文
共 41 条
  • [1] YAH1 of Saccharomyces cerevisiae:: a new essential gene that codes for a protein homologous to human adrenodoxin
    Barros, MH
    Nobrega, FG
    [J]. GENE, 1999, 233 (1-2) : 197 - 203
  • [2] Iron-sulfur clusters: Nature's modular, multipurpose structures
    Beinert, H
    Holm, RH
    Munck, E
    [J]. SCIENCE, 1997, 277 (5326) : 653 - 659
  • [3] Growth in iron-enriched medium partially compensates Escherichia coli for the lack of manganese and iron superoxide dismutase
    Benov, L
    Fridovich, I
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (17) : 10313 - 10316
  • [4] THE COPPER, ZINC-SUPEROXIDE DISMUTASE GENE OF SACCHAROMYCES-CEREVISIAE - CLONING, SEQUENCING, AND BIOLOGICAL-ACTIVITY
    BERMINGHAMMCDONOGH, O
    GRALLA, EB
    VALENTINE, JS
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (13) : 4789 - 4793
  • [5] IS HYDROXYL RADICAL GENERATED BY THE FENTON REACTION INVIVO
    BILINSKI, T
    KRAWIEC, Z
    LICZMANSKI, A
    LITWINSKA, J
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1985, 130 (02) : 533 - 539
  • [6] Brachmann CB, 1998, YEAST, V14, P115
  • [7] O-2-DEPENDENT METHIONINE AUXOTROPHY IN CU,ZN SUPEROXIDE DISMUTASE-DEFICIENT MUTANTS OF SACCHAROMYCES-CEREVISIAE
    CHANG, EC
    KOSMAN, DJ
    [J]. JOURNAL OF BACTERIOLOGY, 1990, 172 (04) : 1840 - 1845
  • [8] MULTIFUNCTIONAL YEAST HIGH-COPY-NUMBER SHUTTLE VECTORS
    CHRISTIANSON, TW
    SIKORSKI, RS
    DANTE, M
    SHERO, JH
    HIETER, P
    [J]. GENE, 1992, 110 (01) : 119 - 122
  • [9] MOLECULAR CHARACTERIZATION OF A COPPER TRANSPORT PROTEIN IN SACCHAROMYCES-CEREVISIAE - AN UNEXPECTED ROLE FOR COPPER IN IRON TRANSPORT
    DANCIS, A
    YUAN, DS
    HAILE, D
    ASKWITH, C
    EIDE, D
    MOEHLE, C
    KAPLAN, J
    KLAUSNER, RD
    [J]. CELL, 1994, 76 (02) : 393 - 402
  • [10] FLINT DH, 1993, J BIOL CHEM, V268, P25547