Metabolism in the Caenorhabditis elegans Mit mutants

被引:42
作者
Rea, SL [1 ]
机构
[1] Univ Colorado, Inst Behav Genet, Boulder, CO 80309 USA
关键词
aging; Caenorhabditis elegans; mitochondria; Mit mutants; oxidative stress; membrane potential; clk-1; isp-1; atp-3; lrs-2;
D O I
10.1016/j.exger.2005.06.015
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
In many eukaryotes oxidative phosphorylation via the mitochondrial electron transport chain provides the major means of ATP production. Complete removal of this capacity often results in premature death. Recent studies using the nematode Caenorhabditis elegans are surprising because they have revealed that disruption of many of the key components of the normal mitochondrial energy-generating machinery do not result in death, rather they result in adult life span extension. Such mutants have been collectively termed Mit mutants. In this short review, the potential use of alternate metabolic pathways for energy generation by Mit mutants will be considered. The effects of using such pathways on residual mitochondrial functionality, reactive radical species production, and longevity will also be explored. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:841 / 849
页数:9
相关论文
共 55 条
[1]   SKN-1 links C-elegans mesendodermal specification to a conserved oxidative stress response [J].
An, JH ;
Blackwell, TK .
GENES & DEVELOPMENT, 2003, 17 (15) :1882-1893
[2]   THE ANAEROBIC END-PRODUCTS OF HELMINTHS [J].
BARRETT, J .
PARASITOLOGY, 1984, 88 (FEB) :179-198
[3]   Assaying metabolic activity in ageing Caenorhabditis elegans [J].
Braeckman, BP ;
Houthoofd, K ;
De Vreese, A ;
Vanfleteren, JR .
MECHANISMS OF AGEING AND DEVELOPMENT, 2002, 123 (2-3) :105-119
[4]  
Brandon MC, 2005, NUCLEIC ACIDS RES, V33, pD611
[5]  
Branicky R, 2000, BIOESSAYS, V22, P48, DOI 10.1002/(SICI)1521-1878(200001)22:1&lt
[6]  
48::AID-BIES9&gt
[7]  
3.0.CO
[8]  
2-F
[9]   Functional F1-ATPase essential in maintaining growth and membrane potential of human mitochondrial DNA-depleted ρ° cells [J].
Buchet, K ;
Godinot, C .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (36) :22983-22989
[10]   PRODUCTION OF SUPEROXIDE RADICALS AND HYDROGEN-PEROXIDE BY NADH-UBIQUINONE REDUCTASE AND UBIQUINOL-CYTOCHROME C REDUCTASE FROM BEEF-HEART MITOCHONDRIA [J].
CADENAS, E ;
BOVERIS, A ;
RAGAN, CI ;
STOPPANI, AOM .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1977, 180 (02) :248-257