Caspase-dependent apoptosis by ectopic expression of E2F-4

被引:14
作者
Chang, YC
Nakajima, H
Illenye, S
Lee, YS
Honjo, N
Makiyama, T
Fujiwara, I
Mizuta, N
Sawai, K
Saida, K
Mitsui, Y
Heintz, NH
Magae, J
机构
[1] Inst Res & Innovat, Kashiwa, Chiba 2770861, Japan
[2] Univ Vermont, Coll Med, Dept Pathol, S Burlington, VT 05403 USA
[3] Natl Inst Biosci & Human Technol, Tsukuba, Ibaraki 3058566, Japan
[4] Kyoto Prefectural Univ Med, Dept Surg 2, Kamikyo Ku, Kyoto 602, Japan
关键词
E2F; apoptosis; cell cycle;
D O I
10.1038/sj.onc.1203833
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
E2F is a family of transcription factors which regulates cell cycle and apoptosis of mammalian cells. E2F-1-3 localize in the nucleus, and preferentially bind pRb, while E2F-4 and 5 have no nuclear localization signal and preferentially bind p107/p130. E2F-6 suppresses the transcriptional activity of other E2F proteins. DP-1 and 2 are heterodimeric partners of each E2F protein. Using tetracycline-responsive promoters, here we compared the effects of ectopic expression of E2F-1, DP-I and E2F-4 on cell cycle progression and apoptosis in Chinese hamster cell lines, We found that E2F-4, as well as DP-I and E2F-1, induced growth arrest and caspase-dependent apoptosis, E2F-4 did not have a marked effect on cell cycle progression, while E2P-1 induced DNA synthesis of resting cells and DP-1 arrested cells in G1, Ectopic expression of E2F-4 did not activate E2F-dependent transcription. Our results suggest that expression of E2F-4 at elevated levels induces growth arrest and apoptosis of mammalian cells through a mechanism distinct from E2F-1 and DP-1.
引用
收藏
页码:4713 / 4720
页数:8
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