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. 2020 Oct 5;295(50):17138–17147. doi: 10.1074/jbc.RA120.014420

Figure 5.

Figure 5.

Neither MARK4wt nor MARK4ΔG316E317D inhibit the TOR pathway or increase autophagic activity. A, MARK4ΔG316E317D did not increase the levels of luciferase coexpressed in fly eyes. Western blots were performed on fly heads expressing luciferase alone (luciferase), coexpressing luciferase and MARK4wt (luciferase+MARK4wt), or coexpressing luciferase and MARK4ΔG316E317D (luciferase+MARK4ΔG316E317D). Actin was used as a loading control. Representative blots and quantitation are shown. Means ± S.D. (error bars); n = 4. n.s. (not significant), p > 0.05; *p < 0.05; **p < 0.01; ***p < 0.005 (one-way ANOVA and Tukey's post-hoc test). BD, expression of MARK4wt or MARK4ΔG316E317D did not promote autophagy. Western blots were performed on fly heads expressing control, MARK4wt, or MARK4ΔG316E317D. Blots were performed with anti-pS6K (pS6K) (B), anti-Ref2P (Ref2P) (C), and LC3 antibody (LC3) (D). Representative blots and quantitation are shown. Means ± S.D. (error bars); n = 3. n.s. (not significant), p > 0.05 (one-way ANOVA and Tukey post-hoc test). Actin was used as a loading control.