Fep1, an iron sensor regulating iron transporter gene expression in Schizosaccharomyces pombe

被引:103
作者
Pelletier, B
Beaudoin, J
Mukai, Y
Labbé, S [1 ]
机构
[1] Univ Sherbrooke, Dept Biochim, Sherbrooke, PQ J1H 5N4, Canada
[2] Osaka Univ, Dept Biotechnol, Suita, Osaka 5650871, Japan
关键词
D O I
10.1074/jbc.M202682200
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
Schizosaccharomyces pombe cells acquire iron under high affinity conditions through the action of a cell surface ferric reductase encoded by the frp1(+) gene and a two-component iron-transporting complex encoded by the fip1(+) and fio1(+) genes. When cells are grown in the presence of iron, transcription of all three genes is blocked. A conserved regulatory element, 5'-(A/T)GATAA-3', located upstream of the frp1(+), fip1(+), and fio1(+) genes, is necessary for iron repression. We have cloned a novel gene, termed fep1(+), which encodes an iron-sensing transcription factor. Binding studies reveal that the putative DNA binding domain of Fep1 expressed as a fusion protein in Escherichia coli specifically interacts with the 5'-(A/T)GATAA-3' sequence in an iron-dependent manner. In a fep1Delta mutant strain, the fio1(+) gene is highly expressed and is unregulated by iron. Furthermore, the fep1Delta mutation increases activity of the cell surface iron reductase and renders cells hypersensitive to the iron-dependent free radical generator phleomycin. Mutations in the transcriptional co-repressors tup11(+) and tup12(+) are phenocopies to fep1(+). Indeed, strains with both tup11Delta and tup12Delta deletions fail to sense iron. This suggests that in the presence of iron and Fep1, the Tup11 and Tup12 proteins may act as co-repressors for down-regulation of genes encoding components of the reductive iron transport machinery.
引用
收藏
页码:22950 / 22958
页数:9
相关论文
共 67 条
[1]   Chemistry and biology of eukaryotic iron metabolism [J].
Aisen, P ;
Enns, C ;
Wessling-Resnick, M .
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 2001, 33 (10) :940-959
[2]  
ALFA C, 1993, EXPT FISSION YEASTS
[3]   The second finger of Urbs1 is required for iron-mediated repression of sid1 in Ustilago maydis [J].
An, ZQ ;
Zhao, Q ;
McEvoy, J ;
Yuan, WM ;
Markley, JL ;
Leong, SA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (11) :5882-5887
[4]   The distal GATA sequences of the sid1 promoter of Ustilago maydis mediate iron repression of siderophore production and interact directly with Urbs1, a GATA family transcription factor [J].
An, ZQ ;
Mei, BG ;
Yuan, WM ;
Leong, SA .
EMBO JOURNAL, 1997, 16 (07) :1742-1750
[5]  
ANDERSON GJ, 1994, ADV EXP MED BIOL, V356, P81
[6]  
Andrews NC, 1999, NUTR REV, V57, P114, DOI 10.1111/j.1753-4887.1999.tb06934.x
[7]   Identification of a Candida albicans ferrichrome transporter and its characterization by expression in Saccharomyces cerevisiae [J].
Ardon, O ;
Bussey, H ;
Philpott, C ;
Ward, DM ;
Davis-Kaplan, S ;
Verroneau, S ;
Jiang, B ;
Kaplan, J .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (46) :43049-43055
[8]  
Askwith C, 1997, J BIOL CHEM, V272, P401
[9]   THE FET3 GENE OF SACCHAROMYCES-CEREVISIAE ENCODES A MULTICOPPER OXIDASE REQUIRED FOR FERROUS IRON UPTAKE [J].
ASKWITH, C ;
EIDE, D ;
VANHO, A ;
BERNARD, PS ;
LI, LT ;
DAVISKAPLAN, S ;
SIPE, DM ;
KAPLAN, J .
CELL, 1994, 76 (02) :403-410
[10]   Molecular biology of iron acquisition in Saccharomyces cerevisiae [J].
Askwith, CC ;
deSilva, D ;
Kaplan, J .
MOLECULAR MICROBIOLOGY, 1996, 20 (01) :27-34