miR-29 miRNAs activate p53 by targeting p85a and CDC42

被引:509
作者
Park, Seong-Yeon [1 ,2 ]
Lee, Jung Hyun [1 ,2 ]
Ha, Minju [1 ,2 ]
Nam, Jin-Wu [1 ,2 ]
Kim, V. Narry [1 ,2 ]
机构
[1] Seoul Natl Univ, Natl Creat Res Ctr, Seoul 151742, South Korea
[2] Seoul Natl Univ, Sch Biol Sci, Seoul 151742, South Korea
关键词
WILD-TYPE P53; GENE-EXPRESSION; LUNG-CANCER; MICRORNAS; RESTORATION; MIR-34A; TRANSACTIVATION; PROFILES; GROWTH;
D O I
10.1038/nsmb.1533
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 p53 is central to many cellular stress responses. Although numerous protein factors that control p53 have been identified, the role of microRNAs (miRNAs) in regulating p53 remains unexplored. In a screen for miRNAs that modulate p53 activity, we find that miR-29 family members (miR-29a, miR-29b and miR-29c) upregulate p53 levels and induce apoptosis in a p53-dependent manner. We further find that miR-29 family members directly suppress p85a (the regulatory subunit of PI3 kinase) and CDC42 (a Rho family GTPase), both of which negatively regulate p53. Our findings provide new insights into the role of miRNAs in the p53 pathway.
引用
收藏
页码:23 / 29
页数:7
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