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. Author manuscript; available in PMC: 2013 Apr 29.
Published in final edited form as: Mitochondrion. 2009 Nov 10;10(2):125–136. doi: 10.1016/j.mito.2009.11.003

Table 1. C. elegans strain description, homology, and lifespan.

The role of in vivo oxidant stress on longevity was studied in three RC subunit missense mutants, three MnSOD knockout mutants, and an insulin receptor missense mutant. FUDR-based median lifespan assessment was largely consistent with previously reported lifespan findings in these strains. * indicates concurrent wild-type (N2 Bristol) control for MnSOD mutant lifespan comparison. All other strains were concurrently studied with the unmarked wild-type (N2 Bristol) control. RC, respiratory chain. Lifespan plots and animal number studied for each mutant are provided in Supplementary Figure 4.

C. elegans Strain Name Gene Function and Human Homologue Mutation Type Human-Worm Protein Similarity Lifespan (20°C)
Interpretation Median Mean Maximum
N2 Bristol - wild-type - vs. RC Mutants
vs. MnSOD mutants*
14
17
16.9
19.9
21
23
gas-1 (fc21) Complex I subunit (NDUFS2) missense 83.4% short-lived 12 15.6 20
mev-1 (kn1) Complex II subunit (SDH-C) missense 75.3% unchanged 14 16.4 22
isp-1 (qm150) Complex III subunit (UQCRFS1) missense 97.5% long-lived 20 22.4 31
daf-2 (e1368) Insulin receptor (IR) missense 62.0% long-lived 31 31.1 38
sod-2 (gk257) Mitochondrial MnSOD (SOD2) - Cel chr. X knockout 97.3% long-lived* 19 20.7 24
sod-2 (ok1030) Mitochondrial MnSOD (SOD2) - Cel chr. X knockout 97.3% long-lived* 20 21.6 25
sod-3 (gk235) Mitochondrial MnSOD (SOD2) - Cel chr. I knockout 97.2% long-lived* 18.5 20.0 23