Deletion of PaAif2 and PaAmid2, two genes encoding mitochondrial AIF-like oxidoreductases of Podospora anserina, leads to increased stress tolerance and lifespan extension

被引:35
作者
Brust, Diana [1 ]
Hamann, Andrea [1 ]
Osiewacz, Heinz D. [1 ]
机构
[1] Goethe Univ Frankfurt, Inst Mol Biosci, Fac Biosci, Cluster Excellence Macromol Complexes, D-60438 Frankfurt, Germany
关键词
Podospora anserina; AIF; Mitochondria; Ageing; Programmed cell death; APOPTOSIS-INDUCING FACTOR; FILAMENTOUS FUNGUS; OXIDATIVE STRESS; SACCHAROMYCES-CEREVISIAE; CELLULAR-LOCALIZATION; ASPERGILLUS-NIDULANS; VITAL FUNCTIONS; COMPLEX-I; SENESCENCE; PROTEIN;
D O I
10.1007/s00294-010-0295-1
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Wild-type strains of the ascomycete Podospora anserina are characterized by a limited lifespan. Mitochondria play a central role in this ageing process raising the question of whether apoptosis-like processes, which are also connected to mitochondrial function, are involved in the control of the final stage in the fungal life cycle. While a role of two metacaspases in apoptosis and lifespan control was recently demonstrated in P. anserina, virtually nothing is known about the function of the protein family of apoptosis-inducing factors (AIFs). Here we report data about proteins belonging to this family. We demonstrate that the cytosolic members PaAIF1 and PaAMID1 do not affect lifespan. In contrast, loss of PaAIF2 and PaAMID2, which both were localized to mitochondria, are characterized by a significantly increased ROS tolerance and a prolonged lifespan. In addition, deletion of PaAmid2 severely affects sporogenesis. These data identify components of a caspase-independent molecular pathway to be involved in developmental processes and in the induction of programmed cell death in the senescent stage of P. anserina.
引用
收藏
页码:225 / 235
页数:11
相关论文
共 62 条
[1]   InterPro - an integrated documentation resource for protein families, domains and functional sites [J].
Apweiler, R ;
Attwood, TK ;
Bairoch, A ;
Bateman, A ;
Birney, E ;
Biswas, M ;
Bucher, P ;
Cerutti, L ;
Corpet, F ;
Croning, MDR ;
Durbin, R ;
Falquet, L ;
Fleischmann, W ;
Gouzy, J ;
Hermjakob, H ;
Hulo, N ;
Jonassen, I ;
Kahn, D ;
Kanapin, A ;
Karavidopoulou, Y ;
Lopez, R ;
Marx, B ;
Mulder, NJ ;
Oinn, TM ;
Pagni, M ;
Servant, F ;
Sigrist, CJA ;
Zdobnov, EM .
BIOINFORMATICS, 2000, 16 (12) :1145-1150
[2]   Flavoprotein disulfide reductases: Advances in chemistry and function [J].
Argyrou, A ;
Blanchard, JS .
PROGRESS IN NUCLEIC ACID RESEARCH AND MOLECULAR BIOLOGY, VOL 78, 2004, 78 :89-142
[3]   Structure-Function of the Cytochrome b6f Complex [J].
Baniulis, D. ;
Yamashita, E. ;
Zhang, H. ;
Hasan, S. S. ;
Cramer, W. A. .
PHOTOCHEMISTRY AND PHOTOBIOLOGY, 2008, 84 (06) :1349-1358
[4]   GRISEA, a copper-modulated transcription factor from Podospora anserina involved in senescence and morphogenesis, is an ortholog of MAC1 in Saccharomyces cerevisiae [J].
Borghouts, C ;
Osiewacz, HD .
MOLECULAR AND GENERAL GENETICS, 1998, 260 (05) :492-502
[5]   Copper-modulated gene expression and senescence in the filamentous fungus Podospora anserina [J].
Borghouts, C ;
Werner, A ;
Elthon, T ;
Osiewacz, HD .
MOLECULAR AND CELLULAR BIOLOGY, 2001, 21 (02) :390-399
[6]   NADPH oxidases NOX-1 and NOX-2 require the regulatory subunit NOR-1 to control cell differentiation and growth in Neurospora crassa [J].
Cano-Dominguez, Nallely ;
Alvarez-Delfin, Karen ;
Hansberg, Wilhelm ;
Aguirre, Jesus .
EUKARYOTIC CELL, 2008, 7 (08) :1352-1361
[7]   Increased resistance of complex I mutants to phytosphingosine-induced programmed cell death [J].
Castro, Ana ;
Lemos, Catarina ;
Falcao, Artur ;
Glass, N. Louise ;
Videira, Arnaldo .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2008, 283 (28) :19314-19321
[8]   A rapid method for efficient gene replacement in the filamentous fungus Aspergillus nidulans [J].
Chaveroche, Marie-Kim ;
Ghigo, Jean-Marc ;
d'Enfert, Christophe .
NUCLEIC ACIDS RESEARCH, 2000, 28 (22) :E97
[9]   Computational method to predict mitochondrially imported proteins and their targeting sequences [J].
Claros, MG ;
Vincens, P .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1996, 241 (03) :779-786
[10]   Complex I is the major site of mitochondrial superoxide production by paraquat [J].
Cocheme, Helena M. ;
Murphy, Michael P. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2008, 283 (04) :1786-1798