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. Author manuscript; available in PMC: 2016 Nov 12.
Published in final edited form as: Oncogene. 2016 Apr 11;35(44):5713–5721. doi: 10.1038/onc.2016.111

Figure 5.

Figure 5

Distinct targets manifest p53-dependent pathologies. (a) Comparative weights of hearts and testes from Mdm2PND/PND, Mdm2PND/PND p53+/−, Mdm2PND/PND p21−/− and Mdm2PND/PND Puma−/− mice. (b) Representative periodic acid–Schiff (PAS)-hematoxylin-stained testes (20×) and ovary (5×) cross-sections from Mdm2PND/PND p53+/−, Mdm2PND/PND p21−/− and hematoxylin and eosin (H&E)-stained section from Mdm2PND/PND Puma−/− mice. (c) Graphical representation of percentage of seminiferous tubule sections containing germ cells of different types in Mdm2PND/PND p53+/−, Mdm2PND/PND p21−/− and Mdm2PND/PND Puma−/− mice testes. (d) Representative picture showing changes in skin pigmentation in Mdm2PND/PND paws after deletion of p53 or after combined deletion of p21 and Puma. *Seminiferous tubules without germ cells; AF, antral follicle; ATF, atreal follicle; CL, corpus luteum; GF, Graffian follicle; PAF, preantral follicle; PF, primary follicle; SF, secondary follicle.

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