| Literature DB >> 18194653 |
Jing Li1, Cong Ran, Edward Li, Faye Gordon, Grant Comstock, Hasan Siddiqui, Whitney Cleghorn, Hui-Zi Chen, Karl Kornacker, Chang-Gong Liu, Shusil K Pandit, Mehrbod Khanizadeh, Michael Weinstein, Gustavo Leone, Alain de Bruin.
Abstract
The E2f7 and E2f8 family members are thought to function as transcriptional repressors important for the control of cell proliferation. Here, we have analyzed the consequences of inactivating E2f7 and E2f8 in mice and show that their individual loss had no significant effect on development. Their combined ablation, however, resulted in massive apoptosis and dilation of blood vessels, culminating in lethality by embryonic day E11.5. A deficiency in E2f7 and E2f8 led to an increase in E2f1 and p53, as well as in many stress-related genes. Homo- and heterodimers of E2F7 and E2F8 were found on target promoters, including E2f1. Importantly, loss of either E2f1 or p53 suppressed the massive apoptosis in double-mutant embryos. These results identify E2F7 and E2F8 as a unique repressive arm of the E2F transcriptional network that is critical for embryonic development and control of the E2F1-p53 apoptotic axis.Entities:
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Year: 2008 PMID： 18194653 PMCID： PMC2253677 DOI： 10.1016/j.devcel.2007.10.017
Source DB: PubMed Journal: Dev Cell ISSN： 1534-5807 Impact factor: 12.270