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. 2004 Aug;24(15):6811–6823. doi: 10.1128/MCB.24.15.6811-6823.2004

TABLE 1.

Genetic interactions among smu-2, smu-1, and unc-52 mutations

Genotypea Developmental stage at onset of paralysis
unc-52(e669su250) Adult
unc-52(e669) Late L4
unc-52(e1012) Late L4
unc-52(e444) Early L4
unc-52(e998) Early L4
unc-52(e1421) Adult
smu-2(mn416) unc-52(e669su250) None
smu-2(mn416) unc-52(e669) Adult
smu-2(mn416) unc-52(e1012) Adult
smu-2(mn416) unc-52(e444) Early L4
smu-2(mn416) unc-52(e998) Early L4
smu-2(mn416) unc-52(e1421) Embryo; adultb
smu-1; unc-52(e669) Adult
smu-1; unc-52(e1012) Adult
smu-1; smu-2(mn416) unc-52(e669) Adult
smu-1; smu-2(mn416) unc-52(e1012) Adult
a

Strains containing e669su250 were grown at 25°C. All others were grown at 20°C.

b

Thirty-seven percent of smu-2 unc-52(e1421) double mutants die as embryos, while 29% of the remaining larvae that hatch show abnormalities consistent with muscle defects. Those embryos that survive to adulthood with no or few abnormalities become uncoordinated at the adult stage in the same manner as unc-52(e1421) mutants.