Correction: The deubiquitinase USP45 inhibits autophagy through actin regulation by Coronin 1B

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Vol. 224, No. 5 | https://doi.org/10.1083/jcb.202407014| March 11, 2025

The authors regret that, in their original article, the wrong version of Fig. 2 I was used. During the revision process, this panel was mistakenly replaced with an older version. The corrected figure is shown here. This error does not affect the conclusions of the study, and the legend of the figure remains unchanged.

In addition, the authors identified typographic errors in the Results section and in several figure legends. The corrected text is shown below.

These errors appear in print and in PDFs downloaded on or before March 26, 2025.

In the Results section, under “Loss of dUsp45 extends lifespan and ameliorates polyQ-induced eye degeneration in Drosophila,” the following text was changed:

To further determine the role of dUsp45 in aging and longevity, we examined the lifespan of dUsp45 mutant flies, including the dUsp45 homozygote P-element insertion mutant (dUsp45^EP1400^/dUsp45^EP1400^dUsp45^EY19835^/dUsp45^EY19835^) and the dUsp45 transheterozygote mutant (dUsp45^EP1400^dUsp45^EY19835^/dUsp45B) (Fig. 8 E).

Figure 3. Mammalian USP45 negatively regulates autophagy.

Figure 4. USP45 negatively regulates lysosomal activity by altering V-ATPase endolysosomal trafficking.

Figure 6. USP45 depletion–induced F-actin patch formation is required for V-ATPase translocation to lysosomes. (A) Confocal microscopy analysis of F-actin structures stained with phalloidin in control (scr) and USP45 knockdown HeLa cells. Arrows indicate cytoplasmic F-actin patches. Scale bar, 20 μm. (B) Quantification of the area of cytoplasmic F-actin patches in A; data shown as mean ± SEM, n = 3, ≥ 35 cells. (C) Immunofluorescence analysis of co-localization of the F-actin patches and endolysosomal markers (EEA1, Rab7, and LAMP2LAMP1) in control and USP45 knockdown cells with indicated antibodies. The scale bars showed 20 μm (original) and 5 μm (zoom-in)insets with 1.5x zoom. (D) Quantification of the colocalization of F-actin patches and endolysosomal markers in C. Pearson’s correlation coefficient was analyzed by ImageJ. Data are shown as mean ± SEM, n = 3, ≥30 cells. (E) Immunofluorescence analysis of colocalization of V-ATPase (V1H) and lysosome (LAMP1) in control and USP45 knockdown HeLa cells treated with LatA (200 nM) or Arp2/3 inhibitor CK666 (200 μM) for 2 h. Scale bar, 10 μm (original) and 5 μm (zoom-in)insets, 2.5x zoom. (F) Quantification of the colocalization of V1H and LAMP1 in E. Pearson’s correlation coefficient and colocalization rate were analyzed by ImageJ. Data are shown as mean ± SEM, n = 3, ≥ 25 cells. (G) Immunofluorescence analysis of colocalization of V-ATPase (V1H) and lysosome (LAMP1) in control and USP45 knockdown cells transfected with control (siCtrl) siRNA or siRNA targeting WASP family genes (siN-WASP and siWASH). Scale bar, 10 μm (original) and 2.5 μm (zoom-in)insets, 2.5x zoom. (H) Quantification of the colocalization of V1H and LAMP1 in G. Data are shown as mean ± SEM, n = 3, ≥ 25 cells. Significance was determined using one-way ANOVA and Dunnett’s (B) or Tukey’s (F and H) multiple comparisons test, and Student’s t test (D); ***P < 0.001; ****P < 0.0001; NS not significant.

Figure 7. Depletion of Coro1B promotes autophagy and V-ATPase lysosomal localization. (A) Confocal images of late L2 larval fat body cells expressing GFP-mCherry-Atg8a in control (Ctrl) and Coro knockdown larvae. Scale bar, 20 μm. (B) Quantification of the ratio of autolysosomes (GFP^−^ mCherry^+^) to total Atg8a puncta per cell in A; data are shown as mean ± S EM, n = 3, ≥20 cells. (C) Confocal images of wL3 larval fat body cells from flies expressing mCherry-Atg8a and indicated transgenes driven by Cg-Gal4. Scale bar, 20 μm. (D) Quantification of Atg8a puncta number and size shown in C. Data are shown as mean ± SEM, n = 3, ≥ 15 cells. (E) Immunofluorescence analysis of colocalization of V-ATPase (V1H) and lysosome (LAMP1) in control and Coro1B knockdown HeLa cells. Scale bar, 20 μm (original) and 2.5 μm (zoom-in)insets, 3x zoom. (F) Quantification of the colocalization of V1H and LAMP1 in E. Pearson’s correlation coefficient and colocalization rate were analyzed by ImageJ. Data are shown as mean ± SEM, n = 3, ≥ 20 cells. (G) Immunofluorescence analysis of colocalization of V-ATPase (V1H) and lysosome (LAMP1) in control and Coro1B knockdown cells treated with LatA (200 nM) or Arp2/3 inhibitor CK666 (200 μM) for 2 h. Scale bar, 20 μm (original) and 5 μm (zoom-in)insets, 2x zoom. (H) Quantification of the colocalization of V1H and LAMP1 in G. Data are shown as mean ± SEM, n = 3, ≥ 25 cells. Significance was determined using one-way ANOVA and Tukey’s multiple comparisons test (D and H), and Student’s t test (B and F); ****P < 0.0001; NS not significant.

Figure 8. Loss of dUsp45 extends lifespan and mitigates polyQ-induced toxicity in Drosophila.

Figure S1. dUsp45 impairs autophagy and V-ATPase translocation to the autolysosome.

Figure S3. USP45 interacts with Coro1B and mediates its ubiquitination. (A) Immunoprecipitation analysis of interaction between Flag-Coro1B and Myc-USP45 bywith Flag antibody. (B) Immunoprecipitation analysis of the interaction between FlagCoro1B and endogenous USP45 bywith pulldown of Flag-Coro1B. (B)(C) RT-PCR analysis of CORO1B mRNA level in control and USP45 knockdown HeLa cell. Quantification of CORO1B mRNA level was normalized to GAPDH. Data are shown as mean ± SEM from three independent experiments. (C)(D) Immunoprecipitation analysis for Flag-Coro1B ubiquitination in HEK293T cells with expression of wild-type (WT) or mutant (C199A) MycUSP45. Cells were lysed by a denaturing agent (1% SDS) containing buffer. Quantification of Ub was normalized to Flag-Coro1B. Data are shown as mean ± SEM from three independent experiments. (D) Significance was determined using one-way ANOVA and Dunnett’s multiple comparisons test (C and D); ****P < 0.0001. Source data are available for this figure: SourceData FS3.