Sign up for Table of Contents Alerts.

Email this page

Print this page

Report

E2F1 and E2F3 activate ATM through distinct mechanisms to promote E1A-induced apoptosis

Sungki Hong, Qiwei X. Paulson and David G. Johnson

Purchase article for $19

Subscribe to this journal for $129/year

Deregulation of the Rb-E2F pathway occurs in many cancers and results in aberrant cell proliferation as well as an increased propensity to undergo apoptosis. In most cases, apoptosis in response to Rb inactivation involves the activation of p53 but the molecular details of the signaling pathway connecting Rb loss to p53 are poorly understood. Here we demonstrate that the E1A oncoprotein, which binds and inhibits Rb family members, induces the accumulation and phosphorylation of p53 through the DNA damage-responsive ATM kinase. As a result, E1A-induced apoptosis is significantly impaired in cells lacking ATM. In contrast, inactivation of ARF, which is widely believed to activate p53 in response to oncogenic stress, has no effect on p53 induction and only a modest effect on apoptosis in response to E1A. Both E2F1 and E2F3 contribute to ATM-dependent phosphorylation of p53 and apoptosis in cells expressing E1A. However, deregulated E2F3 activity is implicated in the DNA damage caused by E1A while E2F1 stimulates ATM- and NBS1-dependent p53 phosphorylation and apoptosis through a mechanism that does not involve DNA damage.

Authors

Sungki Hong

University of Texas MD Anderson Cancer Center; Smithville, TX

Qiwei X. Paulson

University of Texas MD Anderson Cancer Center; Smithville, TX

David G. Johnson

University of Texas MD Anderson Cancer Center; Smithville, TX

Purchase article for $19

Subscribe to this journal for $129/year