Inhibitory Function of p21 Cip1/WAF1 in Differentiation of Primary Mouse Keratinocytes Independent of Cell Cycle Control

Author:

Di Cunto Ferdinando123,Topley Gabrielle123,Calautti Enzo123,Hsiao Jimmy123,Ong Lydia123,Seth Prem K.123,Dotto G. Paolo123

Affiliation:

1. F. Di Cunto, Cutaneous Biology Research Center, Massachusetts General Hospital and Harvard Medical School, 13th Street, Charlestown, MA 02129, USA, and Department of Biology, Genetics and Medical Chemistry, University of Torino, Via Santena 5 bis, Torino, Italy.

2. G. Topley, E. Calautti, J. Hsiao, L. Ong, G. P. Dotto, Cutaneous Biology Research Center, Massachusetts General Hospital and Harvard Medical School, 13th Street, Charlestown, MA 02129, USA.

3. P. K. Seth, Breast Cancer Section, Medicine Branch, National Cancer Institute, Building 10, Bethesda, MD 20892, USA.

Abstract

The cyclin-dependent kinase inhibitor p21 Cip1/WAF1 has been implicated as an inducer of differentiation. However, although expression of p21 is increased in postmitotic cells immediately adjacent to the proliferative compartment, its expression is decreased in cells further along the differentiation program. Expression of the p21 protein was decreased in terminally differentiated primary keratinocytes of mice, and this occurred by a proteasome-dependent pathway. Forced expression of p21 in these cells inhibited the expression of markers of terminal differentiation at both the protein and messenger RNA levels. These inhibitory effects on differentiation were not observed with a carboxyl-terminal truncation mutant or with the unrelated cyclin-dependent kinase inhibitor p16 INK4a , although all these molecules exerted similar inhibition of cell growth. These findings reveal an inhibitory role of p21 in the late stages of differentiation that does not result from the effects of p21 on the cell cycle.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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