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Deletion of putative apoptosis factors leads to lifespan extension in the fungal ageing model Podospora anserina
Author(s) -
Hamann Andrea,
Brust Diana,
Osiewacz Heinz D.
Publication year - 2007
Publication title -
molecular microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.857
H-Index - 247
eISSN - 1365-2958
pISSN - 0950-382X
DOI - 10.1111/j.1365-2958.2007.05839.x
Subject(s) - podospora anserina , biology , senescence , ageing , protease , reactive oxygen species , genetics , microbiology and biotechnology , mutant , mitochondrion , wild type , biochemistry , enzyme , gene
Summary Podospora anserina is a filamentous fungus with a limited lifespan. After a strain‐specific period of growth, cultures turn to senescence and ultimately die. Here we provide evidence that the last step in the ageing of P. anserina is not accidental but programmed. In this study, PaAMID1, a homologue of a mammalian ‘AIF‐homologous mitochondrion‐associated inducer of death’, was analysed as a putative member of a caspase‐independent signalling pathway. In addition, two metacaspases, PaMCA1 and PaMCA2, were investigated. While deletion of PaAmid1 as well as of PaMca2 was found to result in a moderate lifespan extension (59% and 78%, respectively), a 148% increase in lifespan was observed after deletion of PaMca1 . Measurement of arginine‐specific protease activity demonstrates a metacaspase‐dependent activity in senescent but not in juvenile cultures, pointing to an activation of these proteases in the senescent stage of the life cycle. Moreover, treatment of juvenile wild‐type cultures with hydrogen peroxide leads to a PaMCA1‐dependent activity. The presented data strongly suggest that death of senescent wild‐type cultures is triggered by an apoptotic programme induced by an age‐dependent increase of reactive oxygen species during ageing of cultures and is executed after metacaspase activation.