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. 2019 Mar 21;15(9):1592–1605. doi: 10.1080/15548627.2019.1586258

Figure 6.

Figure 6.

The protein-selective effects of autophagy in ATG7−/− and ATG5−/− cells are not explained by genetic compensation. (a) Autophagy-dependent turnover rates (h−1) of mitochondrial proteins from ATG7−/− fibroblasts with and without evidence of proteasomal turnover (ubiquitinated [Ub] sites) [48]. Red lines indicate means; n  =  44 proteins with ubiquitinated sites, 167 without. (b) Autophagy-dependent turnover rates (h−1) of mitochondrial proteins from ATG5−/− fibroblasts with (n  =  45) and without (n  =  151) ubiquitinated sites, as in panel A. (c) Autophagy-dependent turnover rates (h−1) of individual mitochondrial proteins from ATG7−/− fibroblasts with (n  =  31) and without (n  =  180) degrons for mitochondrial proteases Lon and YME1L1. (d) Autophagy-dependent turnover rates (h−1) of individual mitochondrial proteins from ATG5−/− fibroblasts with and without protease degrons (n  =  30 proteins with degrons, 166 without). All comparisons of means in panels A through D are nonsignificant by Student t test.