Table 2. Maximum-likelihood estimates of the logistic model mortality parameters for short- and long-lived C. elegans mutant and N2 control strains.
N2 | Mutant | ||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Gene(s) | Allele(s) | Median life span (D) | n | ln(A) | G | L | Median life span (D) | n | ln(A) | G | L | Effect on life span | Source |
hsf-1 | sy441 | 20 | 42 | −8.00 | 0.342 | 0.282 | 12 | 42 | −7.98 | 0.633 | 1.441 | 0.600 | Hajdu-Cronin et al. (2004) |
gas-1 | fc21 | 19 | 100 | −8.61 | 0.426 | 1.358 | 12 | 100 | −7.87 | 0.668 | 2.442 | 0.632 | Suthammarak et al. (2013) |
skn-1 | zu129 | 15 | 75 | −6.49 | 0.371 | 1.535 | 10 | 75 | −24.72 | 3.093 | 11.184 | 0.667 | An and Blackwell (2003) |
mev-1 | kn1 | 19 | 100 | −8.61 | 0.426 | 1.358 | 13 | 100 | −5.35 | 0.291 | 0.226 | 0.684 | Suthammarak et al. (2013) |
jnk-1 | gk7 | 16 | 386 | −8.90 | 0.537 | 1.997 | 12 | 333 | −14.39 | 1.270 | 4.723 | 0.750 | Ezekowitz (2014) |
daf-16 | m26 | 20 | 19 | −7.54 | 0.345 | 1.186 | 15 | 37 | −14.57 | 0.995 | 3.603 | 0.750 | Kenyon et al. (1993) |
jkk-1 | km2 | 16 | 386 | −8.90 | 0.537 | 1.997 | 13 | 189 | −13.51 | 1.063 | 2.651 | 0.813 | Ezekowitz (2014) |
sir-2.1 | ok434 | 19 | 70 | −5.63 | 0.188 | 0.000 | 16 | 94 | −7.28 | 0.358 | 0.014 | 0.842 | Berdichevsky et al. (2006) |
clk-2 | qm37 | 18 | 50a | −14.95 | 0.839 | 2.666 | 18 | 50a | −14.93 | 0.945 | 6.160 | 1.000 | Van Raamsdonk et al. (2010) |
ctbp-1 | ok498 | 19 | 254 | −7.35 | 0.325 | 0.659 | 22 | 236 | −8.52 | 0.330 | 0.492 | 1.158 | Chen et al. (2009) |
cep-1 | gk138 | 17 | 115 | −9.33 | 0.493 | 0.856 | 20 | 116 | −10.08 | 0.496 | 2.446 | 1.176 | Tavernarakis et al. (2008) |
age-1 | hx546 | 34 | 50 | −7.18 | 0.142 | 0.000 | 42 | 50 | −6.94 | 0.110 | 0.000 | 1.235 | Yanase et al. (2002) |
clk-5 | qm152 | 18 | 50a | −14.95 | 0.839 | 2.666 | 24 | 50a | −14.83 | 0.585 | 2.479 | 1.333 | Van Raamsdonk et al. (2010) |
clk-8 | qm162 | 18 | 50a | −14.95 | 0.839 | 2.666 | 24 | 50a | −8.57 | 0.325 | 1.383 | 1.333 | Van Raamsdonk et al. (2010) |
daf-19 | m86 | 18 | 347 | −8.45 | 0.475 | 2.471 | 24 | 35 | −6.96 | 0.203 | 0.258 | 1.333 | Apfeld and Kenyon (1999) |
mec-8 | e398 | 18 | 347 | −8.45 | 0.475 | 2.471 | 24 | 46 | −8.08 | 0.219 | 0.996 | 1.333 | Apfeld and Kenyon (1999) |
egl-30 | ad806 | 18 | 50 | −19.95 | 1.502 | 9.977 | 25 | 62 | −6.12 | 0.146 | 0.000 | 1.389 | Ch’ng et al. (2008) |
arr-1 | ok401 | 12 | 180 | −5.38 | 0.331 | 0.457 | 17 | 210 | −4.83 | 0.176 | 0.075 | 1.417 | Palmitessa and Benovic (2010) |
cdc-48.1; atx-3 | tm544;gk193 | 19 | 312 | −7.24 | 0.317 | 0.704 | 27 | 222 | −6.95 | 0.184 | 0.382 | 1.421 | Kuhlbrodt et al. (2011) |
clk-3 | qm38 | 18 | 50a | −14.95 | 0.839 | 2.666 | 26 | 50a | −10.41 | 0.341 | 0.884 | 1.444 | Van Raamsdonk et al. (2010) |
clk-1 | qm30 | 18 | 309 | −8.91 | 0.451 | 0.982 | 26 | 112 | −21.52 | 0.903 | 7.037 | 1.444 | Van Raamsdonk and Hekimi (2009) |
che-13 | e1805 | 18 | 347 | −8.45 | 0.475 | 2.471 | 26 | 36 | −5.89 | 0.142 | 0.206 | 1.444 | Apfeld and Kenyon (1999) |
che-2 | e1033 | 18 | 347 | −8.45 | 0.475 | 2.471 | 26 | 33 | −25.00 | 1.560 | 19.645 | 1.444 | Apfeld and Kenyon (1999) |
daf-6 | e1377 | 18 | 347 | −8.45 | 0.475 | 2.471 | 26 | 75 | −5.83 | 0.138 | 0.193 | 1.444 | Apfeld and Kenyon (1999) |
osm-1 | p808 | 18 | 347 | −8.45 | 0.475 | 2.471 | 26 | 17 | −7.21 | 0.195 | 0.000 | 1.444 | Apfeld and Kenyon (1999) |
daf-4 | e1364 | 15 | 60 | −13.21 | 0.851 | 1.699 | 22 | 71 | −11.14 | 0.479 | 1.927 | 1.467 | Shaw et al. (2007) |
nuo-6 | qm200 | 22 | 150 | −12.51 | 0.535 | 0.818 | 33 | 120 | −10.38 | 0.288 | 1.743 | 1.500 | Yang and Hekimi (2010) |
clk-10 | qm169 | 18 | 50a | −14.95 | 0.839 | 2.666 | 28 | 50a | −6.66 | 0.154 | 0.292 | 1.556 | Van Raamsdonk et al. (2010) |
clk-6 | qm158 | 18 | 50a | −14.95 | 0.839 | 2.666 | 28 | 50a | −11.78 | 0.398 | 2.622 | 1.556 | Van Raamsdonk et al. (2010) |
clk-9 | qm164 | 18 | 50a | −14.95 | 0.839 | 2.666 | 28 | 50a | −10.79 | 0.354 | 1.282 | 1.556 | Van Raamsdonk et al. (2010) |
sod-2 | ok1030 | 18 | 309 | −8.91 | 0.451 | 0.982 | 28 | 373 | −8.44 | 0.255 | 0.805 | 1.556 | Van Raamsdonk and Hekimi (2009) |
che-11 | e1810 | 18 | 347 | −8.45 | 0.475 | 2.471 | 28 | 27 | −6.02 | 0.126 | 0.000 | 1.556 | Apfeld and Kenyon (1999) |
daf-10 | e1387 | 18 | 347 | −8.45 | 0.475 | 2.471 | 29 | 30 | −8.89 | 0.252 | 0.877 | 1.611 | Apfeld and Kenyon (1999) |
osm-6 | p811 | 18 | 347 | −8.45 | 0.475 | 2.471 | 30 | 30 | −8.53 | 0.220 | 0.000 | 1.667 | Apfeld and Kenyon (1999) |
clk-7 | qm159 | 18 | 50a | −14.95 | 0.839 | 2.666 | 32 | 50a | −8.03 | 0.212 | 1.109 | 1.778 | Van Raamsdonk et al. (2010) |
osm-3 | p802 | 18 | 347 | −8.45 | 0.475 | 2.471 | 32 | 133 | −7.86 | 0.195 | 0.556 | 1.778 | Apfeld and Kenyon (1999) |
egl-3 | nr2090 | 18 | 46 | −11.13 | 0.704 | 4.043 | 32 | 63 | −7.27 | 0.163 | 0.452 | 1.778 | Ch’ng et al. (2008) |
clk-4 | qm151 | 18 | 50a | −14.95 | 0.839 | 2.666 | 34 | 50a | −5.99 | 0.095 | 0.033 | 1.889 | Van Raamsdonk et al. (2010) |
eat-2 | ad1116 | 18 | 309 | −8.91 | 0.451 | 0.982 | 35 | 156 | −13.18 | 0.366 | 2.838 | 1.944 | Van Raamsdonk and Hekimi (2009) |
tax-4 | p678 | 18 | 347 | −8.45 | 0.475 | 2.471 | 37 | 105 | −8.90 | 0.186 | 0.299 | 2.056 | Apfeld and Kenyon (1999) |
che-3 | p801 | 18 | 347 | −8.45 | 0.475 | 2.471 | 40 | 31 | −9.17 | 0.192 | 0.509 | 2.222 | Apfeld and Kenyon (1999) |
isp-1 | qm150 | 18 | 309 | −8.91 | 0.451 | 0.982 | 42 | 114 | −6.66 | 0.097 | 0.487 | 2.333 | Van Raamsdonk and Hekimi (2009) |
clk-1; sod-2 | ok1030 | 18 | 309 | −8.91 | 0.451 | 0.982 | 44 | 147 | −9.36 | 0.169 | 0.687 | 2.444 | Van Raamsdonk and Hekimi (2009) |
osm-5 | p813 | 18 | 347 | −8.45 | 0.475 | 2.471 | 44 | 46 | −6.74 | 0.092 | 0.000 | 2.444 | Apfeld and Kenyon (1999) |
daf-2; clk-9 | e1370; qm164 | 21 | 200b | −7.72 | 0.303 | 0.265 | 59 | 200b | −8.43 | 0.130 | 0.429 | 2.810 | Van Raamsdonk et al. (2010) |
daf-2; clk-2 | e1370; qm37 | 15 | 200b | −10.90 | 0.720 | 2.747 | 48 | 200b | −6.08 | 0.055 | 0.313 | 3.200 | Van Raamsdonk et al. (2010) |
daf-2 | e1370 | 18 | 309 | −8.91 | 0.451 | 0.982 | 63 | 168 | −7.38 | 0.074 | 0.000 | 3.500 | Van Raamsdonk and Hekimi (2009) |
Note that some mutant strains were compared to the same N2.
Twenty worms per plate were examined with three trials per strain.
Sum of at least three independent trials and an initial number of 80 worms per strain per trial.