Stability of the LATS2 Tumor Suppressor Gene Is Regulated by Tristetraprolin

被引:43
|
作者
Lee, Hyun Hee
Vo, Mai-Tram
Kim, Hyo Jeong
Lee, Unn Hwa
Kim, Chae Won
Kim, Hong Kyeung
Ko, Myoung Seok [1 ]
Lee, Won Hyuck [1 ]
Cha, Seung Joo [2 ]
Min, Young Joo [2 ,3 ]
Choi, Dae Hwa [4 ]
Suh, Ho Seok [5 ]
Lee, Byung Ju
Park, Jeong Woo
Cho, Wha Ja [2 ]
机构
[1] Univ Ulsan, Dept Biol Sci, Ulsan 680749, South Korea
[2] Univ Ulsan, Coll Med, Ulsan Univ Hosp, Biomed Res Ctr, Ulsan 682060, South Korea
[3] Univ Ulsan, Coll Med, Ulsan Univ Hosp, Dept Internal Med, Ulsan 682060, South Korea
[4] Univ Ulsan, Coll Med, Ulsan Univ Hosp, Dept Surg, Ulsan 682060, South Korea
[5] Univ Ulsan, Coll Med, Ulsan Univ Hosp, Dept Dermatol, Ulsan 682060, South Korea
基金
新加坡国家研究基金会;
关键词
ENDOTHELIAL GROWTH-FACTOR; MESSENGER-RNA TURNOVER; AU-RICH ELEMENTS; DOWN-REGULATION; HUMAN HOMOLOG; PROMOTER HYPERMETHYLATION; DROSOPHILA LATS; PROTEIN; EXPRESSION; PROLIFERATION;
D O I
10.1074/jbc.M109.094235
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
LATS2 is a tumor suppressor gene implicated in the control of cell growth and the cell cycle. Here, we investigated the post-transcriptional regulation of LATS2 expression by tristetraprolin (TTP). Our results show that the expression level of LATS2 is inversely correlated with TTP expression in human cancer cell lines. Overexpression of TTP reduced the expression level of LATS2. Conversely, treatment with small interfering RNA against TTP increased the expression level of LATS2 through stabilization of LATS2 mRNA and suppressed the proliferation of A549 human lung cancer cells. LATS2 mRNA contains AU-rich elements (AREs) within the 3'-untranslated region, and TTP destabilized a luciferase mRNA containing LATS2 ARE. In addition, RNA electrophoretic mobility shift assay revealed that TTP directly bound to the ARE of LATS2 mRNA. These results establish LATS2 mRNA as a physiological target of TTP and suggest the possibility that TTP controls cell growth through regulation of LATS2 mRNA stability.
引用
收藏
页码:17329 / 17337
页数:9
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