Regulation of miR-34b/c-targeted gene expression program by SUMOylation

被引:20
|
作者
Li, Yi-Jia [1 ]
Du, Li [1 ]
Aldana-Masangkay, Grace [1 ]
Wang, Xiuli [2 ]
Urak, Ryan [2 ]
Forman, Stephen J. [2 ]
Rosen, Steven T. [2 ]
Chen, Yuan [1 ]
机构
[1] Beckman Res Inst City Hope, Dept Mol Med, Duarte, CA 91010 USA
[2] Beckman Res Inst City Hope, Dept Hematol & Hematopoiet Cell Transplantat, Duarte, CA 91010 USA
关键词
FORKHEAD TRANSCRIPTION FACTOR; SUMO-BINDING MOTIF; MULTIPLE-MYELOMA; CELL-PROLIFERATION; BREAST-CANCER; IN-VIVO; MYC; TUMORIGENESIS; TARGET; LYMPHOMA;
D O I
10.1093/nar/gky484
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 miR-34 family of microRNAs suppresses the expression of proteins involved in pluripotency and oncogenesis. miR-34 expression is frequently reduced in cancers; however, the regulation of their expression is not well understood. We used genome-wide miRNA profiling and mechanistic analysis to show that SUMOylation regulates miR-34b/c expression, which impacts the expression of c-Myc and other tested miR-34 targets. We used site directed mutagenesis and other methods to show that protein kinase B (also known as Akt) phosphorylation of FOXO3a plays an important role in SUMOylation-dependent expression of miR-34b/c. This study reveals how the miR-34-targeted gene expression program is regulated by SUMOylation and shows that SUMOylation need not regulate target proteins through direct modification, but instead can act through the expression of their targeting miRNAs.
引用
收藏
页码:7108 / 7123
页数:16
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