Author:
Doonan Ryan,McElwee Joshua J.,Matthijssens Filip,Walker Glenda A.,Houthoofd Koen,Back Patricia,Matscheski Andrea,Vanfleteren Jacques R.,Gems David
Abstract
The superoxide radical (O2−) has long been considered a major cause of aging. O2− in cytosolic, extracellular, and mitochondrial pools is detoxified by dedicated superoxide dismutase (SOD) isoforms. We tested the impact of each SOD isoform in Caenorhabditis elegans by manipulating its five sod genes and saw no major effects on life span. sod genes are not required for daf-2 insulin/IGF-1 receptor mutant longevity. However, loss of the extracellular Cu/ZnSOD sod-4 enhances daf-2 longevity and constitutive diapause, suggesting a signaling role for sod-4. Overall, these findings imply that O2− is not a major determinant of aging in C. elegans.
Publisher
Cold Spring Harbor Laboratory
Subject
Developmental Biology,Genetics
Cited by
404 articles.
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