MOLECULAR CHARACTERIZATION OF A COPPER TRANSPORT PROTEIN IN SACCHAROMYCES-CEREVISIAE - AN UNEXPECTED ROLE FOR COPPER IN IRON TRANSPORT

被引:578
作者
DANCIS, A
YUAN, DS
HAILE, D
ASKWITH, C
EIDE, D
MOEHLE, C
KAPLAN, J
KLAUSNER, RD
机构
[1] UNIV UTAH, COLL MED, DEPT PATHOL, DIV CELL BIOL & IMMUNOL, SALT LAKE CITY, UT 84132 USA
[2] UNIV MINNESOTA, SCH MED, DEPT BIOCHEM & MOLEC BIOL, DULUTH, MN 55812 USA
[3] NICHHD, MOLEC GENET LAB, BETHESDA, MD 20892 USA
关键词
D O I
10.1016/0092-8674(94)90345-X
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
We report the identification and characterization of CTR1, a gene in the yeast S. cerevisiae that encodes a multispanning plasma membrane protein specifically required for high affinity copper transport into the cell. The predicted protein contains a methionine- and serine-rich domain that includes 11 examples of the sequence Met-X2-Met, a motif noted in proteins involved in bacterial copper metabolism. CTR1 mutants and deletion strains have profound deficiency in ferrous iron uptake, thus revealing a requirement for copper in mediating ferrous transport into the cell. Genetic evidence suggests that the target for this requirement is the FET3 gene (detailed in a companion study), predicted to encode a copper-containing protein that acts as a cytosolic ferro-oxidase. These findings provide an unexpected mechanistic link between the uptake of copper and iron.
引用
收藏
页码:393 / 402
页数:10
相关论文
共 43 条
[1]   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
[2]  
Cammack R, 1990, IRON TRANSPORT STORA, P17
[3]  
CAROLINE D, 1987, NUCLEIC ACIDS RES, V15, P4655
[4]   STUDIES ON COPPER METABOLISM .17. FURTHER OBSERVATIONS ON THE ANEMIA OF COPPER DEFICIENCY IN SWINE [J].
CARTWRIGHT, GE ;
GUBLER, CJ ;
BUSH, JA ;
WINTROBE, MM .
BLOOD, 1956, 11 (02) :143-153
[5]   COPPER RESISTANCE IN PSEUDOMONAS-SYRINGAE MEDIATED BY PERIPLASMIC AND OUTER-MEMBRANE PROTEINS [J].
CHA, JS ;
COOKSEY, DA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (20) :8915-8919
[6]  
COOPER T, 1982, MOL BIOL YEAST SACCH, P436
[7]   FERRIC REDUCTASE OF SACCHAROMYCES-CEREVISIAE - MOLECULAR CHARACTERIZATION, ROLE IN IRON UPTAKE, AND TRANSCRIPTIONAL CONTROL BY IRON [J].
DANCIS, A ;
ROMAN, DG ;
ANDERSON, GJ ;
HINNEBUSCH, AG ;
KLAUSNER, RD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (09) :3869-3873
[8]   GENETIC-EVIDENCE THAT FERRIC REDUCTASE IS REQUIRED FOR IRON UPTAKE IN SACCHAROMYCES-CEREVISIAE [J].
DANCIS, A ;
KLAUSNER, RD ;
HINNEBUSCH, AG ;
BARRIOCANAL, JG .
MOLECULAR AND CELLULAR BIOLOGY, 1990, 10 (05) :2294-2301
[9]   A COMPREHENSIVE SET OF SEQUENCE-ANALYSIS PROGRAMS FOR THE VAX [J].
DEVEREUX, J ;
HAEBERLI, P ;
SMITHIES, O .
NUCLEIC ACIDS RESEARCH, 1984, 12 (01) :387-395
[10]  
EIDE D, 1992, J BIOL CHEM, V267, P20774