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. 1999 Oct;10(10):3279–3288. doi: 10.1091/mbc.10.10.3279

Figure 2.

Figure 2

p21cip1 interacts with p34cdc2/cyclin complexes and does not inhibit the MAPK pathway. (A–D) Recovery of complexes bound to p21cip1. Thirty prophase (P) or metaphase II (MII) oocytes were microinjected or not with p21cip1 to an internal concentration of 1 μM and cultured for 1 h. After homogenization of oocytes, glutathione-agarose beads were added to the clear supernatant. Beads were washed, and bound proteins were electrophoresed and subjected to Western blot analysis for p34cdc2 (A), cyclin B1 (B), cyclin B2 (C), and cyclin A (D). (E) Effect of p21cip1 on the MAPK electrophoretic mobility shift induced by injection of MBP-Mos. Twenty prophase oocytes were microinjected or not with p21cip1 (1 μM). One hour later, they were microinjected with 50 μg of recombinant MBP-Mos or treated with progesterone (Pg). Oocytes were collected at the time of 100% GVBD in MBP-Mos–injected oocytes. An amount equivalent to three oocytes was subjected to Western blot analysis for MAPK.