E2F-1 functions in mice to promote apoptosis and suppress proliferation

被引:709
作者
Field, SJ
Tsai, FY
Kuo, F
Zubiaga, AM
Kaelin, WG
Livingston, DM
Orkin, SH
Greenberg, ME
机构
[1] CHILDRENS HOSP,DIV NEUROSCI,BOSTON,MA 02115
[2] CHILDRENS HOSP,DIV HEMATOL ONCOL,BOSTON,MA 02115
[3] BRIGHAM & WOMENS HOSP,DEPT PATHOL,BOSTON,MA 02115
[4] HOWARD HUGHES MED INST,BOSTON,MA 02115
[5] HARVARD UNIV,SCH MED,DEPT NEUROBIOL,BOSTON,MA 02115
[6] DANA FARBER CANC INST,BOSTON,MA 02115
关键词
D O I
10.1016/S0092-8674(00)81255-6
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
Members of the E2F transcription factor family (E2F-1-E2F-5) are believed to be critical positive regulators of cell cycle progression in eukaryotes although the in vivo functions of the individual E2Fs have not been elucidated. Mice were generated that lack E2F-1 and, surprisingly, these mice develop and reproduce normally. However, E2F-1(-/-) mice exhibit a defect in T lymphocyte development leading to an excess of mature T cells due to a maturation stage-specific defect in thymocyte apoptosis. As E2F-1(-/-) mice age they exhibit a second phenotype marked by aberrant cell proliferation. These findings suggest that while certain members of the E2F family may positively regulate cell cycle progression, E2F-1 functions to regulate apoptosis and to suppress cell proliferation.
引用
收藏
页码:549 / 561
页数:13
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