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Publication : E2F3 is a mediator of DNA damage-induced apoptosis.

First Author  Martinez LA Year  2010
Journal  Mol Cell Biol Volume  30
Issue  2 Pages  524-36
PubMed ID  19917728 Mgi Jnum  J:156401
Mgi Id  MGI:4420502 Doi  10.1128/MCB.00938-09
Citation  Martinez LA, et al. (2010) E2F3 is a mediator of DNA damage-induced apoptosis. Mol Cell Biol 30(2):524-36
abstractText  The E2F transcription factors have emerged as critical apoptotic effectors. Herein we report that the E2F family member E2F3a can be induced by DNA damage through transcriptional and posttranslational mechanisms. We demonstrate that the posttranslational induction of human E2F3a is dependent on the checkpoint kinases. Moreover, we show that human E2F3a is a substrate for the checkpoint kinases (chk kinases) and that mutation of the chk phosphorylation site eliminates the DNA damage inducibility of the protein. Furthermore, we demonstrate that E2F1 and E2F2 are transcriptionally induced by DNA damage in an E2f3-dependent manner. Finally, using both in vitro and in vivo approaches, we establish that E2f3 is required for DNA damage-induced apoptosis. Thus, our data reveal the novel ability of E2f3 to function as a master regulator of the DNA damage response.
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