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1.
Ann N Y Acad Sci ; 1197: 54-66, 2010 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-20536834

RESUMO

Work from more than 50 years of research has unraveled a number of molecular pathways that are involved in controlling aging of the fungal model system Podospora anserina. Early research revealed that wild-type strain aging is linked to gross reorganization of the mitochondrial DNA. Later it was shown that aging of P. anserina does also take place, although at a slower pace, when the wild-type specific mitochondrial DNA rearrangements do not occur. Now it is clear that a network of different pathways is involved in the control of aging. Branches of these pathways appear to be connected and constitute a hierarchical system of responses. Although cross talk between the individual pathways seems to be fundamental in the coordination of the overall system, the precise underlying interactions remain to be unraveled. Such a systematic approach aims at a holistic understanding of the process of biological aging, the ultimate goal of modern systems biology.


Assuntos
Envelhecimento/fisiologia , Mitocôndrias/metabolismo , Modelos Biológicos , Podospora/fisiologia , Envelhecimento/genética , Envelhecimento/metabolismo , Fenômenos Bioquímicos , DNA Mitocondrial/genética , DNA Mitocondrial/metabolismo , DNA Mitocondrial/fisiologia , Mitocôndrias/genética , Mitocôndrias/fisiologia , Podospora/genética , Podospora/metabolismo
2.
Aging (Albany NY) ; 1(3): 328-34, 2009 Mar 03.
Artigo em Inglês | MEDLINE | ID: mdl-20157520

RESUMO

PaMTH1 is an O-methyltransferase catalysing the methylation of vicinal hydroxyl groups of polyphenols. The protein accumulates during ageing of Podospora anserina in both the cytosol and in the mitochondrial matrix. The construction and characterisation of a PaMth1 deletion strain provided additional evidence about the function of the protein in the protection against metal induced oxidative stress. Deletion of PaMth1 was found to lead to a decreased resistance against exogenous oxidative stress and to a shortened lifespan suggesting a role of PaMTH1 as a longevity assurance factor in a new molecular pathway involved in lifespan control.


Assuntos
Proteínas Fúngicas/fisiologia , Metiltransferases/fisiologia , Estresse Oxidativo , Podospora/enzimologia , Podospora/crescimento & desenvolvimento , Sulfato de Cobre/metabolismo , Citosol/enzimologia , Deleção de Genes , Peróxido de Hidrogênio/metabolismo , Redes e Vias Metabólicas , Mitocôndrias/enzimologia , Podospora/química , Espécies Reativas de Oxigênio
3.
Aging Cell ; 7(5): 651-62, 2008 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-18616635

RESUMO

PaMTH1, a putative methyltransferase previously described to increase in abundance in total protein extracts during aging of Podospora anserina is demonstrated to accumulate in the mitochondrial cell fraction of senescent cultures. The protein is localized in the mitochondrial matrix and displays a methyltransferase activity utilizing flavonoids as substrates. Constitutive over-expression of PaMth1 in P. anserina results in a reduced carbonylation of proteins and an extended lifespan without impairing vital functions suggesting a protecting role of PaMTH1 against oxidative stress.


Assuntos
Proteínas Fúngicas/biossíntese , Proteínas Fúngicas/genética , Regulação Fúngica da Expressão Gênica/fisiologia , Metiltransferases/biossíntese , Metiltransferases/genética , Podospora/enzimologia , Podospora/crescimento & desenvolvimento , S-Adenosilmetionina/fisiologia , Animais , Proteínas Fúngicas/classificação , Proteínas Fúngicas/fisiologia , Humanos , Metiltransferases/classificação , Metiltransferases/fisiologia , Proteínas Mitocondriais/biossíntese , Proteínas Mitocondriais/classificação , Proteínas Mitocondriais/genética , Proteínas Mitocondriais/fisiologia , Estresse Oxidativo/genética , Estresse Oxidativo/fisiologia , Podospora/genética , Podospora/fisiologia , Ratos , Fatores de Tempo
4.
Exp Gerontol ; 42(9): 887-98, 2007 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-17689904

RESUMO

According to the 'free radical theory of ageing', the generation and accumulation of reactive oxygen species are key events during ageing of biological systems. Mitochondria are a major source of ROS and prominent targets for ROS-induced damage. Whereas mitochondrial DNA and membranes were shown to be oxidatively modified with ageing, mitochondrial protein oxidation is not well understood. The purpose of this study was an unbiased investigation of age-related changes in mitochondrial proteins and the molecular pathways by which ROS-induced protein oxidation may disturb cellular homeostasis. In a differential comparison of mitochondrial proteins from young and senescent strains of the fungal ageing model Podospora anserina, from brains of young (5 months) vs. older rats (17 and 31 months), and human cells, with normal and chemically accelerated in vitro ageing, we found certain redundant posttranslationally modified isoforms of subunits of ATP synthase affected across all three species. These appear to represent general susceptible hot spot targets for oxidative chemical changes of proteins accumulating during ageing, and potentially initiating various age-related pathologies and processes. This type of modification is discussed using the example of SAM-dependent O-methyltransferase from P. anserina (PaMTH1), which surprisingly was found to be enriched in mitochondrial preparations of senescent cultures.


Assuntos
Envelhecimento/fisiologia , Mitocôndrias/química , ATPases Mitocondriais Próton-Translocadoras/análise , Isoformas de Proteínas/análise , Proteoma , Animais , Células Cultivadas , Eletroforese em Gel Bidimensional , Proteínas Fúngicas/análise , Humanos , Metiltransferases/análise , Modelos Biológicos , Estresse Oxidativo , Podospora/fisiologia , Processamento de Proteína Pós-Traducional , Ratos , Espécies Reativas de Oxigênio/metabolismo , Espectrometria de Massas por Ionização e Dessorção a Laser Assistida por Matriz
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