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1.
Mech Ageing Dev ; 131(5): 315-22, 2010 May.
Article in English | MEDLINE | ID: mdl-20226205

ABSTRACT

With uniparental inheritance of mitochondria, there seems little reason for homologous recombination in mitochondria, but the machinery for mitochondrial recombination is quite well-conserved in many eukaryote species. In fungi and yeasts heteroplasmons may be formed when strains fuse and transfer of organelles takes place, making it possible to study mitochondrial recombination when introduced mitochondria contain different markers. A survey of wild-type isolates from a local population of the filamentous fungus Podospora anserina for the presence of seven optional mitochondrial introns indicated that mitochondrial recombination does take place in nature. Moreover the recombination frequency appeared to be correlated with age: the more rapidly ageing fraction of the population had a significantly lower linkage disequilibrium indicating more recombination. Direct confrontation experiments with heterokaryon incompatible strains with different mitochondrial markers at different (relative) age confirmed that mitochondrial recombination increases with age. We propose that with increasing mitochondrial damage over time, mitochondrial recombination - even within a homoplasmic population of mitochondria - is a mechanism that may restore mitochondrial function.


Subject(s)
Cellular Senescence/genetics , DNA, Mitochondrial/genetics , Mitochondria/genetics , Podospora/physiology , Recombination, Genetic , Introns , Podospora/genetics
2.
Exp Gerontol ; 45(7-8): 516-24, 2010 Aug.
Article in English | MEDLINE | ID: mdl-20064602

ABSTRACT

Calorie restriction (CR) is a regimen of reduced food intake that, although the underlying mechanism is unknown, in many organisms leads to life span extension. Podospora anserina is one of the few known ageing filamentous fungi and the ageing process and concomitant degeneration of mitochondria have been well-studied. CR in P. anserina increases not only life span but also forestalls the ageing-related decline in fertility. Here we review what is known about CR in P. anserina and about possibly involved mechanisms like enhanced mitochondrial stability, reduced production of reactive oxygen species and changes in the OXPHOS machinery. Additionally, we present new microscopic data on mitochondrial dynamics under rich nutritional and CR conditions at different points in life. Lines that have grown under severe CR for more than 50x the normal life span, show no accumulation of age-related damage, though fecundity is reduced in some of these lines. Finally, we discuss the possible role of CR in P. anserina in nature and the effect of CR at different points in life.


Subject(s)
Podospora/metabolism , Biological Evolution , DNA, Fungal/genetics , DNA, Fungal/metabolism , DNA, Mitochondrial/genetics , DNA, Mitochondrial/metabolism , Genetic Variation , Glucose/metabolism , Lipofuscin/metabolism , Mitochondria/metabolism , Models, Biological , Phenotype , Plasmids/genetics , Podospora/genetics , Podospora/growth & development , Reactive Oxygen Species/metabolism
3.
Mech Ageing Dev ; 131(1): 60-8, 2010 Jan.
Article in English | MEDLINE | ID: mdl-20026344

ABSTRACT

Although most fungi appear to be immortal, some show systemic senescence within a distinct time frame. Podospora anserina for example shows an irreversible growth arrest within weeks of culturing associated with a destabilization of the mitochondrial genome. Here, we show that calorie restriction (CR), a regimen of under-nutrition without malnutrition, increases not only life span but also forestalls the aging-related decline in fertility. Similar to respiratory chain deficiencies the life span extension is associated with lower levels of intracellular H(2)O(2) measurements and a stabilization of the mitochondrial genome. Unlike respiratory chain deficiencies, CR cultures have a wild-type-like OXPHOS machinery similar to that of well-fed cultures as shown by native electrophoresis of mitochondrial protein complexes. Together, these data indicate that life span extension via CR is fundamentally different from that via respiratory chain mutations: Whereas the latter can be seen as a pathology, the former promotes healthy life span extension and may be an adaptive response.


Subject(s)
Caloric Restriction , Mitochondria/metabolism , Podospora/physiology , Adaptation, Physiological , DNA, Mitochondrial/metabolism , Fertility , Genomic Instability , Glucose/deficiency , Hydrogen Peroxide/metabolism , Oxidative Phosphorylation , Time Factors
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