Volume 28, Issue 5, Pages e4 (March 2018)

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Volume 28, Issue 5, Pages 753-760.e4 (March 2018) Insulin Signaling Regulates Oocyte Quality Maintenance with Age via Cathepsin B Activity  Nicole M. Templeman, Shijing Luo, Rachel Kaletsky, Cheng Shi, Jasmine Ashraf, William Keyes, Coleen T. Murphy  Current Biology  Volume 28, Issue 5, Pages 753-760.e4 (March 2018) DOI: 10.1016/j.cub.2018.01.052 Copyright © 2018 Elsevier Ltd Terms and Conditions

Figure 1 Characterization of daf-2(−) Oocyte Gene Expression (A) daf-2 RNAi extends fem-1(hc17) mated reproductive span (n = 59–60; p < 0.0001). (B and C) Eight independent expression comparisons of day 8 daf-2(RNAi);fem-1(hc17) versus fem-1(hc17) oocytes reveal 126 upregulated genes (B) and 30 downregulated genes (C); FDR = 1%; ranked by significance (SAM). See also Data S1. (D and E) Overlap between oocyte-specific and whole-worm gene sets that are (D) upregulated with daf-2 RNAi and (E) downregulated with daf-2 RNAi (FDR = 1%; see also Figures S1D and S1E and Data S2). (F) Percentages of unhatched embryos (orange) and unfertilized oocytes (green) produced daily from mated daf-2(e1370) mutant worms treated with RNAis against top-scoring genes upregulated in daf-2(RNAi) oocytes. Normal progeny are not displayed. p values are differences in unhatched embryo production with age between target gene RNAi-treated group versus control RNAi-treated group. See also Figure S2. (G) Loss of pqm-1 decreases daf-2(e1370) self-fertilized reproductive span by 50% (n = 40; ∗∗∗∗p < 0.0001). Current Biology 2018 28, 753-760.e4DOI: (10.1016/j.cub.2018.01.052) Copyright © 2018 Elsevier Ltd Terms and Conditions

Figure 2 Cathepsin-B-like Cysteine Proteases Inhibit Oocyte Quality Maintenance with Age (A) Unlike other members of the clan CA of cysteine proteases, a group of cathepsin-B-like genes are significantly downregulated in day 8 daf-2(RNAi);fem-1(hc17) oocytes (FDR = 1%; ranked by SAM significance score). (B) Cathepsin B protease activity (Magic Red Cathepsin B Kit) of the most mature unfertilized oocyte of day 1 and mated day 7 wild-type and daf-2(1370) (±SEM; n = 18–22 individuals; see Figure S3B for representative images). (C and D) Representative images (C) and scored oocyte morphology defects (D) show significant improvements in oocyte quality for day 5 mated rrf-3(pk1426) worms with life-long feeding of W07B8.4(RNAi) versus control (L4440 vector) RNAi (n = 73–88). For reference, a young (day 2) mated rrf-3(pk1426) worm on control RNAi is shown; no obvious differences were noted in the oocyte morphology of day 2 W07B8.4(RNAi) versus control RNAi worms. ∗p ≤ 0.05; ∗∗∗∗p < 0.0001. Current Biology 2018 28, 753-760.e4DOI: (10.1016/j.cub.2018.01.052) Copyright © 2018 Elsevier Ltd Terms and Conditions

Figure 3 Inhibition of Cathepsin-B-like Cysteine Proteases Reduces Age-Dependent Oocyte Quality Deterioration (A and B) Representative images (A) and oocyte morphology defect scoring (B) show that MDL-28170 treatment after day 1 of adulthood significantly improves day 5 mated wild-type oocyte quality compared to DMSO-exposed controls (n = 72–75). (C and D) Representative images (C) and oocyte morphology defect scoring (D) show that MDL-28170 after day 3 of adulthood significantly improves oocyte quality of day 7 mated wild-type worms compared to DMSO-exposed controls (n = 45–49). White arrows indicate oocytes. (E) Oocyte morphology scoring of day 7 mated wild-type worms treated from day 3 of adulthood onward with DMSO control (n = 39), the cathepsin B + calpain inhibitor MDL-28170 (n = 30), or the calpain inhibitor PD-150606 (n = 41) indicates that MDL-28170 treatment in mid-reproduction significantly improves oocyte quality, unlike PD-150606. ∗p ≤ 0.05; ∗∗p < 0.01; ∗∗∗p < 0.001; ∗∗∗∗p < 0.0001 in comparison with DMSO control group. Current Biology 2018 28, 753-760.e4DOI: (10.1016/j.cub.2018.01.052) Copyright © 2018 Elsevier Ltd Terms and Conditions