Cellular copper homeostasis, mitochondrial DNA instabilities, and lifespan control in the filamentous fungus Podospora anserina

Experimental Gerontology

Volumn 35, Issue 6-7, 2000, Pages 677-686

  Osiewacz, H D ^a   Borghouts, C ^a  

^a GOETHE UNIVERSITY   (Germany)

Author keywords

Aging; Cellular copper homeostasis; Homologous recombination; Mitochondrial DNA; Podospora anserina; Respiration

Indexed keywords

COPPER; DNA TOPOISOMERASE (ATP HYDROLYSING); MITOCHONDRIAL DNA; REACTIVE OXYGEN METABOLITE; TRANSCRIPTION FACTOR;

CELL NUCLEUS; CONFERENCE PAPER; COPPER METABOLISM; GENE MUTATION; HOMEOSTASIS; LIFESPAN; MITOCHONDRION; NONHUMAN; OPEN READING FRAME; PODOSPORA ANSERINA; PRIORITY JOURNAL; RESPIRATORY CHAIN;

COPPER; DNA, MITOCHONDRIAL; HOMEOSTASIS; INTRONS; MITOCHONDRIA; SPHAERIALES; SUPPORT, NON-U.S. GOV'T;

FUNGI; PODOSPORA ANSERINA;

EID: 0033788297     PISSN: 05315565     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0531-5565(00)00142-X     Document Type: Conference Paper

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6. GRISEA, a copper-modulated transcription factor from Podospora anserina involved in senescence and morphogenesis, is an ortholog of MAC1 in Saccharomyces cerevisiae
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