Effects of deleting mitochondrial Antioxidant genes on life span

dc.contributor.authorÜnlü, Ercan Selçuk
dc.contributor.authorKoç, Ahmet
dc.date.accessioned2017-06-18T08:52:42Z
dc.date.available2017-06-18T08:52:42Z
dc.date.issued2007
dc.departmentİnönü Üniversitesien_US
dc.descriptionAnn N Y Acad Sci., (1100), 505–0.en_US
dc.description.abstractReactive oxygen species (ROS) damage biomolecules, accelerate aging, and shorten life span, whereas antioxidant enzymes mitigate these effects. Because mitochondria are a primary site of ROS generation and also a primary target of ROS attack, they have become a major focus area of aging studies. Here, we employed yeast genetics to identify mitochondrial antioxidant genes that are important for replicative life span. In our studies, it was found that among the known mitochondrial antioxidant genes (TTR1, CCD1, SOD1, GLO4, TRR2, TRX3, CCS1, SOD2, GRX5, PRX1), deletion of only three genes, SOD1 (Cu, Zn superoxide dismutase), SOD2 (Manganese-containing superoxide dismutase), and CCS1 (Copper chaperone), shortened the life span enormously. The life span decreased 40% forΔsod1 mutant, 72% forΔsod2 mutant, and 50% forΔccs1 mutant. Deletion of the other genes had little or no effect on life span.en_US
dc.identifier.citationÜnlü, E. S., & Koç, A. (2007). Effects Of Deleting Mitochondrial Antioxidant Genes On Life Span . Ann N Y Acad Sci., (1100), 505–0.en_US
dc.identifier.endpage0en_US
dc.identifier.issue0en_US
dc.identifier.startpage0en_US
dc.identifier.urihttps://hdl.handle.net/11616/7098
dc.identifier.volume0en_US
dc.language.isoenen_US
dc.publisherAnn N Y Acad Sci.en_US
dc.relation.ispartofAnn N Y Acad Sci.en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectAgingen_US
dc.subjectAntioxidant genesen_US
dc.subjectMitochondriaen_US
dc.subjectROSen_US
dc.subjectCCS1en_US
dc.titleEffects of deleting mitochondrial Antioxidant genes on life spanen_US
dc.typeArticleen_US

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