Myc-ARF (alternate reading frame) interaction inhibits the functions of Myc

被引:107
作者
Datta, A
Nag, A
Pan, W
Hay, N
Gartel, AL
Colamonici, O
Mori, Y
Raychaudhuri, P
机构
[1] Univ Illinois, Dept Biochem & Mol Genet, Chicago, IL 60607 USA
[2] Univ Illinois, Rheumatol Sect, Chicago, IL 60607 USA
[3] Univ Illinois, Dept Pharmacol, Chicago, IL 60612 USA
关键词
D O I
10.1074/jbc.M312305200
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
The tumor suppressor protein ARF (alternate reading frame) inhibits MDM2 to stabilize and activate the functions of p53. Here we provide evidence for an additional activity of ARF that attenuates cell cycle progression independently of p53 activation. We show that ARF interacts with c-Myc independently of MDM2 or p53. Consequently, ARF relocalizes c-Myc from the nucleoplasm to the nucleolus. Binding and relocalization by ARF correlate with an inhibition of the c-Myc-activated transcription in both p53-positive and -negative cells. Using inducible cell lines, we show that the wild type ARF, but not a mutant, inhibits expression of the c-Myc-induced genes before inhibiting S phase. Moreover, ARF inhibits Myc-induced progression into S phase in cells lacking p53 or expressing a defective p53, indicating that ARF inhibits the S phase stimulatory function of c-Myc independently of p53. Our results strongly suggest that c-Myc is a bona fide target of ARF and that ARF attenuates c-Myc independently of the ARF-p53 axis.
引用
收藏
页码:36698 / 36707
页数:10
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