Role of YHM1, encoding a mitochondrial carrier protein, in iron distribution of yeast

被引:19
作者
Lesuisse, E
Lyver, ER
Knight, SAB
Dancis, A
机构
[1] Univ Paris 07, Inst Jacques Monod, Lab Ingn Prot Prot & Controle Metab, F-75251 Paris 05, France
[2] Univ Paris 06, Inst Jacques Monod, Lab Ingn Prot Prot & Controle Metab, F-75251 Paris 05, France
[3] Univ Penn, Dept Med, Div Hematol Oncol, Philadelphia, PA 19104 USA
关键词
carrier protein; haem; iron; mitochondria; Saccharomyces; yeast;
D O I
10.1042/BJ20031387
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
Mitochondrial carrier proteins are a large protein family, consisting of 35 members in Saccharomyces cerevisiae. Members of this protein family have been shown to transport varied substrates from cytoplasm to mitochondria or mitochondria to cytoplasm, although many family members do not have assigned substrates. We speculated whether one or more of these transporters will play a role in iron metabolism. Haploid yeast strains each deleted for a single mitochondrial carrier protein were analysed for alterations in iron homoeostasis. The strain deleted for YHM1 was characterized by increased and misregulated surface ferric reductase and high-affinity ferrous transport activities. Siderophore uptake from different sources was also increased, and these effects were dependent on the AFT1 iron sensor regulator. Mutants of YHM1 converted into rhodegrees, consistent with secondary mitochondrial DNA damage from mitochondrial iron accumulation. In fact, in the Deltayhm1 mutant, iron was found to accumulate in mitochondria. The accumulated iron showed decreased availability for haem synthesis, measured in isolated mitochondria using endogenously available metals and added porphyrins. The phenotypes of Deltayhm1 mutants indicate a role for this mitochondrial transporter in cellular iron homoeostasis.
引用
收藏
页码:599 / 607
页数:9
相关论文
共 48 条
[1]   Iron and copper transport in yeast and its relevance to human disease [J].
Askwith, C ;
Kaplan, J .
TRENDS IN BIOCHEMICAL SCIENCES, 1998, 23 (04) :135-138
[2]   The yeast mitochondrial transport proteins: new sequences and consensus residues, lack of direct relation between consensus residues and transmembrane helices, expression patterns of the transport protein genes, and protein-protein interactions with other proteins [J].
Belenkiy, R ;
Haefele, A ;
Eisen, MB ;
Wohlrab, H .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 2000, 1467 (01) :207-218
[3]   Aft2p, a novel iron-regulated transcription activator that modulates, with Aft1p, intracellular iron use and resistance to oxidative stress in yeast. [J].
Blaiseau, PL ;
Lesuisse, E ;
Camadro, JM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (36) :34221-34226
[4]  
BRITTENHAM G, 2000, DISORDERS IRON METAB, P397
[5]   PURIFICATION AND PROPERTIES OF COPROPORPHYRINOGEN OXIDASE FROM THE YEAST SACCHAROMYCES-CEREVISIAE [J].
CAMADRO, JM ;
CHAMBON, H ;
JOLLES, J ;
LABBE, P .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1986, 156 (03) :579-587
[6]   CCC1 suppresses mitochondrial damage in the yeast model of Friedreich's ataxia by limiting mitochondrial iron accumulation [J].
Chen, OS ;
Kaplan, J .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (11) :7626-7632
[7]   Mitochondrial iron metabolism in the yeast Saccharomyces cerevisiae [J].
Craig, EA ;
Voisine, C ;
Schilke, B .
BIOLOGICAL CHEMISTRY, 1999, 380 (10) :1167-1173
[8]   Terminal steps of haem biosynthesis [J].
Dailey, HA .
BIOCHEMICAL SOCIETY TRANSACTIONS, 2002, 30 :590-595
[9]   MOLECULAR CHARACTERIZATION OF A COPPER TRANSPORT PROTEIN IN SACCHAROMYCES-CEREVISIAE - AN UNEXPECTED ROLE FOR COPPER IN IRON TRANSPORT [J].
DANCIS, A ;
YUAN, DS ;
HAILE, D ;
ASKWITH, C ;
EIDE, D ;
MOEHLE, C ;
KAPLAN, J ;
KLAUSNER, RD .
CELL, 1994, 76 (02) :393-402
[10]   Presence of a member of the mitochondrial carrier family in hydrogenosomes:: Conservation of membrane-targeting pathways between hydrogenosomes and mitochondria [J].
Dyall, SD ;
Koehler, CM ;
Delgadillo-Correa, MG ;
Bradley, PJ ;
Plümper, E ;
Leuenberger, D ;
Turck, CW ;
Johnson, PJ .
MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (07) :2488-2497