Role for the p53 homologue p73 in E2F-1-induced apoptosis

被引:525
|
作者
Irwin, M
Marin, MC
Phillips, AC
Seelan, RS
Smith, DI
Liu, WG
Flores, ER
Tsai, KY
Jacks, T
Vousden, KH
Kaelin, WG
机构
[1] Harvard Univ, Sch Med, Dana Farber Canc Inst, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Brigham & Womens Hosp, Boston, MA 02115 USA
[3] NCI, Regulat Cell Growth Lab, FCRDC, Frederick, MD 21702 USA
[4] Mayo Clin & Mayo Fdn, Mayo Med Sch, Dept Lab Med & Pathol, Rochester, MN 55905 USA
[5] MIT, Dept Biol, Cambridge, MA 02139 USA
[6] MIT, Ctr Canc Res, Cambridge, MA 02139 USA
[7] Howard Hughes Med Inst, Chevy Chase, MD 20185 USA
关键词
D O I
10.1038/35036614
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The transcription factor E2F-1 induces both cell-cycle progression and, in certain settings, apoptosis. E2F-1 uses both p53-dependent and p53-independent pathways to kill cells(1-8). The p53-dependent pathway involves the induction by E2F-1 of the human tumour-suppressor protein p14ARF, which neutralizes HDM2 (human homologue of MDM2) and thereby stabilizes the p53 protein(9). Here we show that E2F-1 induces the transcription of the p53 homologue p73. Disruption of p73 function inhibited E2F-1-induced apoptosis in p53-defective tumour cells and in p53(-/-) mouse embryo fibroblasts. We conclude that activation of p73 provides a means for E2F-1 to induce death in the absence of p53.
引用
收藏
页码:645 / 648
页数:5
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