Intraspecific variation in survival and mitochondrial oxidative phosphorylation in wild-caught Drosophila simulans

被引:38
作者
Melvin, Richard G.
Ballard, J. William O. [1 ]
机构
[1] Univ New S Wales, Sch Biotechnol & Biomol Sci, Ramaciotti Ctr Gene Funct Anal, Sydney, NSW 2052, Australia
[2] Univ Iowa, Roy J Carver Ctr Comparat Gen, Dept Biol Sci, Iowa City, IA 52242 USA
关键词
aging; Drosophila simulans; efficiency; mitochondria; OXPHOS;
D O I
10.1111/j.1474-9726.2006.00211.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Lifespans of organisms vary greatly even among individuals of the same species. Under the framework of the free oxygen radical theory of aging, it is predicted that variation in individual lifespan within a species will correlate with variation in the accumulation of oxidative damage to cell components from reactive oxygen species. In this study we test the hypothesis that variation in survival of three wild-caught Drosophila simulans fly lines (HW09, NC48 and MD106) correlates with three key aspects of mitochondrial bioenergetics. The rank order of median survival was HW09 > MD106 > NC48. Young HW09 flies (11-18 days) had (i) highest ADP:O (quantity of oxygen consumed by mitochondria when provided with a quantity of ADP) when metabolizing both electron transport chain complex I and complex III substrates; (ii) lowest rate of mitochondrial hydrogen peroxide production from complex III; and (iii) highest cytochrome c oxidase activity from complex IV. Rate of hydrogen peroxide production increased and cytochrome c oxidase activity decreased in all lines in the age range 11-25 days. This is the first study to correlate natural variation in organism survival with natural variation in mitochondrial bioenergetics.
引用
收藏
页码:225 / 233
页数:9
相关论文
共 50 条
[1]   Comparative genomics of mitochondrial DNA in Drosophila simulans [J].
Ballard, JWO .
JOURNAL OF MOLECULAR EVOLUTION, 2000, 51 (01) :64-75
[2]   Mitochondrial oxygen radical generation and leak: Sites of production in state 4 and 3, organ specificity, and relation to aging and longevity [J].
Barja, G .
JOURNAL OF BIOENERGETICS AND BIOMEMBRANES, 1999, 31 (04) :347-366
[3]   Uncoupling to survive? The role of mitochondrial inefficiency in ageing [J].
Brand, MD .
EXPERIMENTAL GERONTOLOGY, 2000, 35 (6-7) :811-820
[4]   RAPID ENZYME KINETIC ASSAYS OF INDIVIDUAL DROSOPHILA AND COMPARISONS OF FIELD-CAUGHT DROSOPHILA-MELANOGASTER AND DROSOPHILA-SIMULANS [J].
CLARK, AG ;
KEITH, LE .
BIOCHEMICAL GENETICS, 1989, 27 (5-6) :263-277
[5]   Mitochondrial DNA inherited variants are associated with successful aging and longevity in humans [J].
De Benedictis, G ;
Rose, G ;
Carrieri, G ;
De Luca, M ;
Falcone, E ;
Passarino, G ;
Bonafé, M ;
Monti, D ;
Baggio, G ;
Bertolini, S ;
Mari, D ;
Mattace, R ;
Franceschi, C .
FASEB JOURNAL, 1999, 13 (12) :1532-1536
[6]   Variation in cytochrome-c oxidase activity is not maternally inherited in the copepod Tigriopus californicus [J].
Edmands, S ;
Burton, R .
HEREDITY, 1998, 80 :668-674
[7]  
Edmands S, 1999, EVOLUTION, V53, P1972, DOI 10.1111/j.1558-5646.1999.tb04578.x
[8]  
Estabrook R.W., 1967, METHOD ENZYMOL, V10, P41, DOI DOI 10.1016/0076-6879(67)10010-4
[9]   The respiratory chain complex thresholds in mitochondria of a Drosophila subobscura mutant strain [J].
Farge, G ;
Touraille, S ;
Debise, R ;
Alziari, S .
BIOCHIMIE, 2002, 84 (12) :1189-1197
[10]   Age-associated decline in mitochondrial respiration and electron transport in Drosophila melanogaster [J].
Ferguson, M ;
Mockett, RJ ;
Shen, Y ;
Orr, WC ;
Sohal, RS .
BIOCHEMICAL JOURNAL, 2005, 390 (02) :501-511