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. 1998 Jul;9(7):1817–1831. doi: 10.1091/mbc.9.7.1817

Figure 1.

Figure 1

The PP1 inhibitor I-2 does not prevent activation of mitotic cyclin B proteolysis. (A) Dose–response curve showing the effect of different concentrations of I-2 on the dephosphorylation of 32P-labeled glycogen phosphorylase A in Xenopus interphase extracts. (B) Dose–response curve showing the effect of different concentrations of OA on the phosphatase activity in Xenopus interphase extracts containing 10 μM I-2 (determined as in A). (C) The stability of 35S-labeled cyclin B was analyzed in extracts entering mitosis in the absence or presence of 10 μM I-2. Entry into mitosis was triggered by addition of nondegradable recombinant cyclin Δ90 at time zero, and samples taken at the indicated time points were analyzed by SDS-PAGE and phosphorimaging.