Copper homeostasis in eukaryotes: Teetering on a tightrope

被引:203
作者
Balamurugan, Kuppusamy [1 ]
Schaffner, Walter [1 ]
机构
[1] Univ Zurich, Inst Mol Biol, CH-8057 Zurich, Switzerland
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH | 2006年 / 1763卷 / 07期
关键词
copper scarcity; copper importers; Ctr1B; copper load; metallothioneins; copper detoxification; MTF-1;
D O I
10.1016/j.bbamcr.2006.05.001
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
The transition metal copper is an essential trace element for both prokaryotes and eukaryotes. However, intracellular free copper has to be strictly limited due to its toxic side effects, not least the generation of reactive oxygen species (ROS) via redox cycling. Thus, all organisms have sophisticated copper homeostasis mechanisms that regulate uptake, distribution, sequestration and export of copper. From insects to mammals, metal-responsive transcription factor (MTF-1), a zinc finger transcription factor, controls expression of metallothioneins and other components involved in heavy metal homeostasis. In the fruit fly Drosophila, MTF-1 paradoxically acts as an activator under both high and low copper concentrations. Namely, under high copper conditions, MTF-1 activates metallothioneins in order to protect the cell, while under low copper conditions MTF-1 activates the copper importer Ctr1B in order to acquire scarce copper from the surroundings. This review highlights the current knowledge of copper homeostasis in eukaryotes with a focus on Drosophila and the role of MTF-1. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:737 / 746
页数:10
相关论文
共 124 条
[1]   Yeast Cox17 solution structure and copper(I) binding [J].
Abajian, C ;
Yatsunyk, LA ;
Ramirez, BE ;
Rosenzweig, AC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (51) :53584-53592
[2]   Regulation of metallothionein gene expression by oxidative stress and metal ions [J].
Andrews, GK .
BIOCHEMICAL PHARMACOLOGY, 2000, 59 (01) :95-104
[3]   Characterization of the binding interface between the copper chaperone Atx1 and the first cytosolic domain of Ccc2 ATPase [J].
Arnesano, F ;
Banci, L ;
Bertini, I ;
Cantini, F ;
Ciofi-Baffoni, S ;
Huffman, DL ;
O'Halloran, TV .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (44) :41365-41376
[4]   Metallothioneins in brain - The role in physiology and pathology [J].
Aschner, M ;
Cherian, MG ;
Klaassen, CD ;
Palmiter, RD ;
Erickson, JC ;
Bush, AI .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1997, 142 (02) :229-242
[5]   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
[6]   Metal-responsive transcription factor (MTF-1) and heavy metal stress response in Drosophila and mammalian cells:: a functional comparison [J].
Balamurugan, K ;
Egli, D ;
Selvaraj, A ;
Zhang, B ;
Georgiev, O ;
Schaffner, W .
BIOLOGICAL CHEMISTRY, 2004, 385 (07) :597-603
[7]   Copper [J].
Barceloux, DG .
JOURNAL OF TOXICOLOGY-CLINICAL TOXICOLOGY, 1999, 37 (02) :217-230
[8]   Oxidative stress and lipid peroxidation-derived DNA-lesions in inflammation driven carcinogenesis [J].
Bartsch, H ;
Nair, J .
CANCER DETECTION AND PREVENTION, 2004, 28 (06) :385-391
[9]  
Bayer TA, 2005, J ALZHEIMERS DIS, V8, P201
[10]   Dietary Cu stabilizes brain superoxide dismutase 1 activity and reduces amyloid Aβ production in APP23 transgenic mice [J].
Bayer, TA ;
Schäfer, S ;
Simons, A ;
Kemmling, A ;
Kamer, T ;
Tepest, R ;
Eckert, A ;
Schüssel, K ;
Eikenberg, O ;
Sturchler-Pierrat, C ;
Abramowski, D ;
Staufenbiel, M ;
Multhaup, G .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (24) :14187-14192