p19ARF targets certain E2F species for degradation

被引:149
作者
Martelli, F
Hamilton, T
Silver, DP
Sharpless, NE
Bardeesy, N
Rokas, M
DePinho, RA
Livingston, DM
Grossman, SR
机构
[1] Dana Farber Canc Inst, Dept Canc Biol, Boston, MA 02115 USA
[2] Dana Farber Canc Inst, Dept Adult Oncol, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Dept Genet, Boston, MA 02115 USA
[4] Harvard Univ, Sch Med, Dept Med, Boston, MA 02115 USA
[5] Brigham & Womens Hosp, Dept Med, Boston, MA 02115 USA
关键词
D O I
10.1073/pnas.081061398
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
p19ARF suppresses the growth of cells lacking p53 through an unknown mechanism. p19ARF was found to complex with transcription factors E2F1, -2, and -3. Levels of endogenous or ectopically expressed E2F1, -2, and -3, but not E2F6, were reduced after synthesis of p19ARF, through a mechanism involving increased turnover. p19ARF-induced degradation of E2F1 depended on a functional proteasome, and E2F1 was relocalized to nucleoli when coexpressed with p19ARF. Consistent with reduced levels of E2F1 and E2F3, the proliferation of cells defective for p53 function was suppressed by p19ARF, and the effect was partially reversed by ectopic overexpression of E2F1. These results suggest a broader role for p19ARF as a tumor suppressor, in which targeting of certain E2F species may cooperate with stimulation of the p53 pathway to counteract oncogenic growth signals.
引用
收藏
页码:4455 / 4460
页数:6
相关论文
共 49 条
[1]   p14ARF links the tumour suppressors RB and p53 [J].
Bates, S ;
Phillips, AC ;
Clark, PA ;
Stott, F ;
Peters, G ;
Ludwig, RL ;
Vousden, KH .
NATURE, 1998, 395 (6698) :124-125
[2]  
Blattner C, 1999, MOL CELL BIOL, V19, P3704
[3]   Regulation of E2F through ubiquitin-proteasome-dependent degradation: Stabilization by the pRB tumor suppressor protein [J].
Campanero, MR ;
Flemington, EK .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (06) :2221-2226
[4]   p16INK4A and p19ARF act in overlapping pathways in cellular immortalization [J].
Carnero, A ;
Hudson, JD ;
Price, CM ;
Beach, DH .
NATURE CELL BIOLOGY, 2000, 2 (03) :148-155
[5]   E2F-6:: a novel member of the E2F family is an inhibitor of E2F-dependent transcription [J].
Cartwright, P ;
Müller, H ;
Wagener, C ;
Holm, K ;
Helin, K .
ONCOGENE, 1998, 17 (05) :611-623
[6]   Cooperative effects of INK4a and ras in melanoma susceptibility in vivo [J].
Chin, L ;
Pomerantz, J ;
Polsky, D ;
Jacobson, M ;
Cohen, C ;
CordonCardo, C ;
Horner, JW ;
DePinho, RA .
GENES & DEVELOPMENT, 1997, 11 (21) :2822-2834
[7]   E1A signaling to p53 involves the p19ARF tumor suppressor [J].
de Stanchina, E ;
McCurrach, ME ;
Zindy, F ;
Shieh, SY ;
Ferbeyre, G ;
Samuelson, AV ;
Prives, C ;
Roussel, MF ;
Sherr, CJ ;
Lowe, SW .
GENES & DEVELOPMENT, 1998, 12 (15) :2434-2442
[8]   Regulation of a senescence checkpoint response by the E2F1 transcription factor and p14ARF tumor suppressor [J].
Dimri, GP ;
Itahana, K ;
Acosta, M ;
Campisi, J .
MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (01) :273-285
[9]   Disruption of the ARF-Mdm2-p53 tumor suppressor pathway in Myc-induced lymphomagenesis [J].
Eischen, CM ;
Weber, JD ;
Roussel, MF ;
Sherr, CJ ;
Cleveland, JL .
GENES & DEVELOPMENT, 1999, 13 (20) :2658-2669
[10]   Unusual proliferation arrest and transcriptional control properties of a newly discovered E2F family member, E2F-6 [J].
Gaubatz, S ;
Wood, JG ;
Livingston, DM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (16) :9190-9195