Table 2.

Activation of EGL-15 perturbs sex muscle differentiation

Genotype% Animals with differentiated sex muscles% Animals with mispositioned-differentiated sex musclesSex muscle Pmyo-3::GFPexpression
N2 100 NA 
ccIs4251; soc-2 100 
soc-2; ayIs15 [egl-15(neu*)] NA +/– 
soc-2 ayIs18 [5B*] 100 63 
soc-2; ayIs27 [5A*] NA +/– 
daf-18(lf) soc-2; ayIs15 100 100 
soc-2; pdk-1(gf) ayIs15 68 63 
soc-2; akt-1(gf); ayIs15 82.5 62 
daf-16(lf); soc-2; ayIs15 20 20 +/– 
Genotype% Animals with differentiated sex muscles% Animals with mispositioned-differentiated sex musclesSex muscle Pmyo-3::GFPexpression
N2 100 NA 
ccIs4251; soc-2 100 
soc-2; ayIs15 [egl-15(neu*)] NA +/– 
soc-2 ayIs18 [5B*] 100 63 
soc-2; ayIs27 [5A*] NA +/– 
daf-18(lf) soc-2; ayIs15 100 100 
soc-2; pdk-1(gf) ayIs15 68 63 
soc-2; akt-1(gf); ayIs15 82.5 62 
daf-16(lf); soc-2; ayIs15 20 20 +/– 

Forty young adult animals were scored for differentiated sex muscles after being fixed and stained with rhodamine-phalloidin.

Alleles used: soc-2(n1774), daf-18(nr2037lf), pdk-1(mg142gf),akt-1(mg144gf) and daf-16(mg54lf). ccIs4251; daf-18(lf), ccIs4251;daf-18(lf) soc-2, pdk-1(gf), akt-1(gf), daf-16(lf) and daf-16(lf);soc-2 animals all have differentiated sex muscles located in wild-type positions in 100% of the animals examined. The presence of the ccIs4251 transgene or the soc-2 mutation has no significant effects on sex muscle differentiation. The daf-18(nr2037)soc-2(n1774) double mutant has a mildly penetrant Egl phenotype and some subtle abnormalities in sex muscle morphology when stained with rhodamine-phalloidin

+, strong GFP expression in the vm1s of all animals; +/–, weak GFP expression in poorly differentiated sex muscles, some animals with no detectable GFP expression. NA, not applicable

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