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Cell Cycle, Cell Death, and Senescene

Multiple Response Elements and Differential p53 Binding Control Perp Expression During Apoptosis¹

¹ Department of Biology and Center for Cancer Research, Massachusetts Institute of Technology, Cambridge, MA;
² Department of Radiation Oncology, Stanford University School of Medicine, Stanford, CA; and
³ Howard Hughes Medical Institute, Chevy Chase, MD

Requests for reprints: Tyler Jacks, Center for Cancer Research, Massachusetts Institute of Technology, Room E17-110, 77 Massachusetts Avenue, Cambridge, MA 02139. Phone: (617) 253-0262; Fax: (617) 253-9863. E-mail: tjacks{at}mit.edu

The p53 tumor suppressor gene responds to cellular stress by activating either cell cycle arrest or apoptosis. A growing number of target genes involved in each of these pathways have been identified. However, the mechanism by which the apoptosis versus arrest decision is made remains to be elucidated. Perp is a proapoptotic target gene of p53 expressed to high levels in apoptotic cells compared with those undergoing cell cycle arrest. This pattern of expression is unusual among p53 target genes, many of which are induced to similar levels during arrest and apoptosis. Here, we describe the regulation of the Perp gene by p53 through at least three response elements in the Perp promoter and first intron. These sites are occupied in vivo in E1A-expressing mouse embryo fibroblasts undergoing apoptosis but not cell cycle arrest, in contrast to the p21 5' response element, which is occupied during both. The apoptosis-deficient p53 point mutant, p53V143A, displays a selective deficit in binding to the Perp elements, demonstrating that p53 can distinguish between Perp and p21 at the level of DNA binding. These results provide mechanistic insight into the selective expression of Perp during apoptosis and may provide a useful model for studying the p53-dependent cell cycle arrest versus apoptosis decision.

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