Interventions

  • Species: + -
  • name effect species mean median maximum
    unc-46 mutation unc-46(e177) allele has no significant effect on lifespan [9789046]. unc-46 mutants are uncoordinated [4366476]. Worm
    unc-47 mutation The unc-47(e367) allele has no significant effect on lifespan [9789046]. unc-47 mutants are uncoordinated [4366476]. Worm
    unc-54 mutation Mutation in unc-54 has no effect on lifespan [9789046]. unc-54 mutants are paralyzed [4366476]. Worm
    unc-6 mutation Mutation in unc-6 has no effect on lifespan [9789046]. unc-6 mutants are uncoordinated [4366476]. Worm
    unc-78 mutation Mutation in unc-78 has no effect on lifespan [9789046]. unc-78 mutants move slowly [7190524]. Worm
    unc-78 mutation Mutation in unc-78 has no effect on lifespan [9789046]. unc-78 mutants move slowly [7190524]. Worm
    unc-79 mutation The unc-79(e1068) allele has no significant effect on lifespan [9789046]. unc-78 mutants display irregular movement [4366476]. Worm
    unc-80 mutation The unc-80(e1069) allele has no significant effect on lifespan [9789046]. unc-80 mutant displays irregular movement [4366476] Worm
    D1054.8 RNAi RNA interference of D1054.8 results in lifespan extension [15998808]. Worm
    him-6 RNAi him-6 mutants have a low brood size, a shortened lifespan, and an increased amount of germ-line apoptosis [16181657]. Worm
    aak-1 mutation aak-1 does not appear to be required for the control of lifespan [15574588]. Worm
    hsp-12.6 mutation hsp-12.6 loss-of-function mutation significantly extends lifespan under AL and significantly suppresses intermittent fasting (IF)-induced increase in lifespan, to a similar extend to that of daf-16 mutation. The extent of IF-induced longevity in daf-16 hsp-12.6 double mutant is similar to that of single hsp-12.6 or daf-16 mutants. hsp-12.6 and daf-16 function in same signaling pathway [19079239]. Worm
    hif-1 mutation hif-1 mutation does not suppress lifespan extension of bDR or eat-2 mutation [19372390]. hif-1 deletion extends lifespan by 24%. hif-1 mutation extends lifespan under AL, but does not further extend lifespan extension under modified sDR. hif-1 mutation does not further extend rsks-1 lifespan. pha-4 RNAi slightly reduces lifespan in wild-type and hif-1 mutants, but hif-1 mutation extends lifespan of animals treated with control or pha-4 RNAi to a similar level [19461873]. Worm
    ire-1 mutation ire-1 mutation reduces slightly the lifespan under AL, but reduces significantly the lifespan extension by DR. ire-1 mutant has a significantly reduced slope in mean lifespan versus food concentrations relative to wild-type. ire-1 mutation fully suppresses lifespan extension by hif-1 mutation under AL and DR conditions [19461873]. Worm
    egl-9 mutation egl-9 deletion does not affect lifespan under AL. Lifespan extension under modified sDR regimen is diminished by egl-9 mutation. egl-9 mutation significantly suppresses the lifespan extension by a strong loss-of-function allele of eat-2. Lifespan extension by deletion mutants of rsks-1 is fully suppressed by egl-9 mutation [19461873]. Worm
    ubc-18 mutation Loss of ubc-18 function by mutation reduces lifespan at 25 degree Celsius, but only slightly at 20 degree Celsius [19553937]. Worm
    cup-4 mutation Lifespan of cup-4 mutants increases only moderately by sDR [19783783]. Worm
    trx-1 mutation Mutants with a deletion in the trx-1 gene display a decrease in lifespan and are sensitive to oxidative stress [16324156]. trx-1 null mutant display reduced mean and maximum lifespan. trx-1 deletion completely suppresses the lifespan extension caused by eat-2 mutation, but only partially suppresses that by daf-2 or osm-5 mutations [16387300]. Worm
    wwp-1 RNAi RNA interference of wwp-1 decreases median lifespan by 9% in wild-type animals and 24% in daf-2 mutants [18006689]. Loss of wwp-1 function by RNAi reduces lifespan at 25 degree Celsius, but not 20 degree Celsius. Reduced levels of wwp-1 completely suppress the extended longevity of eat-2 mutants. wwp-1 RNAi does not suppress the extended lifespan of isp-1 mutants and has only minor suppressive effects on lifespan of another mitochondrial mutant, clk-1, and in cyc-1 RNAi treated worms. RNAi depletion of wwp-1 has no effect on long lifespan of daf-2 mutants [19553937]. Worm -9
    wwp-1 mutation Loss of wwp-1 function by mutation reduces lifespan at 25 degree Celsius, but not 20 degree Celsius. Lifespan of wwp-1 mutants across entire food concentration range by bacterial dilution in liquid culture or on solid plates does not noticeable change. Reduced levels of wwp-1 completely suppress the extended longevity of eat-2 mutants [19553937]. Worm -9
    smk-1 mutation Loss of smk-1 by temperature sensitive allele suppresses the extended lifespan under optimal bDR, but not the response to DR itself [17476212]. Worm
    sir-2.1 deletion sir-2.1 deletion slightly reduces lifespan of wild-type [16860373]. sir-2.1 suppresses longevity of unc-13 and eat-2, but not daf-2 or unc-64 mutants [16860373]. sir-2.1 is therefore partially required for lifespan extension from mutation of eat-2 [16860373], but is completely independent for lifespan extension from DR using a reduced feeding protocol [Kaeberlein et al. in press]. sDR increases lifespan of wild-type and sir-2.1 mutants to the same extent [19239417]. Worm
    pha-4 mutation Mutants of pha-4 do not respond to bacterial DR. Therefore, loss of pha-4 completely blocks the response to varying food concentration. Reduction of pha-4 does not suppress the long lifespan of daf-2 mutants or animals with defective electron transport chain [17476212]. IF significantly extends lifespan of pha-4 [19079239]. sDR extends lifespan of mutants with a temperature sensitive allele of pha-4, but not daf-16 RNAi [19239417]. Worm
    hsf-1 mutation A mutant allele of hsf-1 slightly decreases lifespan under AL, but cancels out the lifespan extension effect of bDR. hsf-1 RNAi also prevents lifespan extension by bDR. Glucose or glycerol does not shorten the lifespan of hsf-1 mutants. Glucose treatment completely suppresses the long lifespan caused by hsf-1 overexpression [19883616]. sDR extends the lifespan of hsf-1 mutant with a premature stop codon, that eliminates activation domain, and that of wild-type to a similar extent [19239417]. Worm
    tdp-1 mutation tdp-1(ok803) mutation increases mean and maximum lifespan at 20 degree Celsius but not at 25 degree Celsius. tdp-1(ok803) reduce the lifespan of daf-2(e1370) mutants, but does not does not reduces the lifespan of daf-16(mu86) mutants [Vaccaro et al. 2012]. Worm
    Interventions are an extension of GenAge and GenDR.