Functional Interplay between RNA-Binding Protein HuR and microRNAs

被引:161
作者
Srikantan, Subramanya [1 ]
Tominaga, Kumiko [1 ]
Gorospe, Myriam [1 ]
机构
[1] NIA, Lab Mol Biol & Immunol, Intramural Res Program, NIH, Baltimore, MD 21224 USA
基金
美国国家卫生研究院;
关键词
Ribonucleoprotein complexes; RNA-binding protein; microRNA; post-transcriptional gene regulation; mRNA decay; translational contro; RISC; MESSENGER-RNA; POSTTRANSCRIPTIONAL REGULATION; TRANSLATIONAL CONTROL; TUMOR-SUPPRESSOR; NUCLEAR EXPORT; KINASE; MIR-34A; P53; PHOSPHORYLATION; REPRESSION;
D O I
10.2174/138920312801619394
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 mammalian RNA-binding protein (RBP) HuR associates with numerous mRNAs encoding proteins with roles in cell division, cell survival, immune response, and differentiation. HuR was known to stabilize many of these mRNAs and/or modulated their translation, but the molecular processes by which HuR affected the fate of target mRNAs was largely unknown. Evidence accumulated over the past five years has revealed that the influence of HuR on many bound transcripts depends on HuR's interplay with microRNAs which associate with the same mRNAs. Here, we review the interactions of HuR and microRNAs - both competitive and cooperative - that govern expression of shared target mRNAs. Competition between HuR and microRNAs typically results in enhanced gene expression if the HuR-mRNA interaction prevails, and in repression if the microRNA remains associated. Cooperation between HuR and microRNAs leads to lower expression of the shared mRNA. We also describe the regulation of HuR levels by microRNAs as well as the regulation of microRNA levels by HuR. Finally, we discuss transcriptome-wide analyses of HuR-bound mRNAs with neighboring microRNA sites, and review the emerging mechanisms whereby microRNAs confer versatility and robustness to the post-transcriptional outcomes of HuR targets.
引用
收藏
页码:372 / 379
页数:8
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