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. 2014 Jul 1;25(13):2071–2083. doi: 10.1091/mbc.E14-01-0015

TABLE 1:

Analysis of germ cell corpses in animals treated with RNAi of candidate lysosomal cathepsins in C. elegans.

Human cathepsin C. elegans cathepsin genes (RNAi) Number of cell corpses in rrf-3(pk1426) mutants (mean ± SEM) Number of germ cell corpses in cpl-1(yq89) mutants (mean ± SEM)
Control RNAi 1.4 ± 0.3
Control RNAi 28.9 ± 1.5
Cathepsin A F13D12.6 1.7 ± 0.5 26.4 ± 1.7
F32A5.3 1.9 ± 0.5 25.4 ± 2.2
F41C3.5 2.2 ± 0.3 27.4 ± 1.5
K10B2.2 1.8 ± 0.4 30.1 ± 1.7
Y16B4A.2 1.9 ± 0.5 29.3 ± 1.6
Y32F6A.5 1.7 ± 0.2 30.1 ± 1.9
K10C2.1 1.7 ± 0.4 33.9 ± 1.7
Y40D12A.2 2.6 ± 0.3 29.6 ± 2.2
Cathepsin D asp-1(Y39B6A.20) 2.9 ± 0.4 32.5 ± 1.8
asp-3(H22K11.1) 1.8 ± 0.4 28.7 ± 2.4
asp-4(R12H7.2) 1.5 ± 0.5 32.9 ± 2.1
Cathepsin B cpr-1(C52E4.1) 1.1 ± 0.3 29.1 ± 1.7
cpr-2(F36D3.9) 1.4 ± 0.2 27.8 ± 2.3
cpr-3(T10H4.12) 1.8 ± 0.4 32.3 ± 2.2
cpr-4(F44C4.3) 1.7 ± 0.4 32.4 ± 1.6
cpr-5(W07B8.5) 2.3 ± 0.4 30.1 ± 1.5
cpr-6(C25B8.3) 2.2 ± 0.3 30.3 ± 2.2
F32H5.1 2.3 ± 0.4 32.9 ± 2.0
F57F5.1 2.5 ± 0.3 30.7 ± 2.0
W07B8.1 2.0 ± 0.2 27.6 ± 2.4
W07B8.4 2.0 ± 0.3 29.0 ± 2.5
Y65B4A.2 1.9 ± 0.2 27.9 ± 1.9
Cathepsin E asp-5(F21F8.3) 2.6 ± 0.5 29.1 ± 2.3
asp-6(F21F8.7) 2.1 ± 0.3 30.1 ± 1.7
asp-9(C11D2.2) 1.7 ± 0.5 31.0 ± 1.9
asp-10(C15C8.3) 2.1 ± 0.4 27.2 ± 1.9
asp-12(F21F8.4) 2.2 ± 0.4 32.4 ± 2.6
asp-19(ZK384.6) 1.6 ± 0.3 33.4 ± 1.7
Cathepsin F R07E3.1 1.7 ± 0.3 31.1 ± 2.3
R09F10.1 3.0 ± 0.6 24.7 ± 1.6
F41E6.6 1.7 ± 0.3 29.2 ± 1.6
Cathepsin H K02E7.10 2.3 ± 0.6 29.8 ± 2.1
tag-329(C50F4.3) 2.5 ± 0.3 31.2 ± 1.9
Cathepsin L Y51A2D.1 2.3 ± 0.6 30.4 ± 1.5
Y51A2D.8 2.3 ± 0.4 26.9 ± 1.4
Y71H2AR.2 2.4 ± 0.4 30.4 ± 2.0
cpl-1(T03E6.7) 25.0 ± 1.6 29.1 ± 2.1
Cathepsin S C32B5.7 1.4 ± 0.2 29.4 ± 2.2
F15D4.4 2.8 ± 0.6 26.8 ± 2.5
Y40H7A.10 1.9 ± 0.2 33.1 ± 1.6
Y71H2AM.25 1.4 ± 0.3 29.8 ± 1.3
Cathepsin Z cpz-1(F32B5.8) 1.3 ± 0.3 32.0 ± 1.9
cpz-2(M04G12.2) 1.7 ± 0.3 28.8 ± 1.5

Germ cell corpses were analyzed in rrf-3(pk1462) adult animals (24 h post L4) grown on RNAi plates at 20°C and in cpl-1(yq89) animals that were grown to L4 molt on RNAi plates at 20°C and then transferred to 25°C for further culture of 24 h. The identity of each RNAi clone was confirmed by sequencing.