AMF1 (GPS2) modulates p53 transactivation

被引:47
作者
Peng, YC [1 ]
Kuo, F [1 ]
Breiding, DE [1 ]
Wang, YF [1 ]
Mansur, CP [1 ]
Androphy, EJ [1 ]
机构
[1] Tufts Univ, Sch Med, New England Med Ctr, Dept Dermatol, Boston, MA 02111 USA
关键词
D O I
10.1128/MCB.21.17.5913-5924.2001
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
We have reported that the papillomavirus E2 protein binds the nuclear factor AMF1 (also called G-protein pathway suppressor 2 or GPS2) and that their interaction is necessary for transcriptional activation by E2. It has also been shown that AMF1 can influence the activity of cellular transcription factors. These observations led us to test whether AMF1 regulates the functions of p53, a critical transcriptional activator that integrates stress signals and regulates cell cycle and programmed cell death. We report that AMF1 associates with p53 in vivo and in vitro and facilitates the p53 response by augmenting p53-dependent transcription. Overexpression of AMF1 in U20S cells increases basal level p21(WAF1/CIP1) expression and causes a G(1) arrest. U20S cells stably overexpressing AMF1 show increased apoptosis upon exposure to UV irradiation. These data demonstrate that AMF1 modulates p53 activities.
引用
收藏
页码:5913 / 5924
页数:12
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