Regulation of the MIR155 host gene in physiological and pathological processes

被引:430
作者
Elton, Terry S. [1 ,2 ,3 ]
Selemon, Helina [1 ]
Elton, Shane M. [6 ]
Parinandi, Narasimham L. [1 ,3 ,4 ,5 ]
机构
[1] Ohio State Univ, Davis Heart & Lung Res Inst, Columbus, OH 43210 USA
[2] Ohio State Univ, Div Pharmacol, Coll Pharm, Columbus, OH 43210 USA
[3] Ohio State Univ, Div Cardiol, Dept Med, Columbus, OH 43210 USA
[4] Ohio State Univ, Lipid Signaling & Lipid Lab, Columbus, OH 43210 USA
[5] Ohio State Univ, Div Pulm Allergy Crit Care & Sleep Med, Columbus, OH 43210 USA
[6] Midwestern Univ, Glendale, AZ USA
关键词
miRNAs; Gene regulation; Hematopoiesis; Immunity; Cancer; Cardiovascular disease; EPSTEIN-BARR-VIRUS; TYPE-1 RECEPTOR EXPRESSION; MICRORNA EXPRESSION; BREAST-CANCER; TARGET GENES; TNF-ALPHA; IN-VIVO; TRANSLATION INITIATION; ALTERED EXPRESSION; DOWN-REGULATION;
D O I
10.1016/j.gene.2012.12.009
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
MicroRNAs (miRNAs), a family of small nonprotein-coding RNAs, play a critical role in posttranscriptional gene regulation by acting as adaptors for the miRNA-induced silencing complex to inhibit gene expression by targeting mRNAs for translational repression and/or cleavage. miR-155-5p and miR-155-3p are processed from the B-cell Integration Cluster (BIC) gene (now designated, MIR155 host gene or MIR155HG). MiR-155-5p is highly expressed in both activated B- and T-cells and in monocytes/macrophages. MiR-155-5p is one of the best characterized miRNAs and recent data indicate that miR-155-5p plays a critical role in various physiological and pathological processes such as hematopoietic lineage differentiation, immunity, inflammation, viral infections, cancer, cardiovascular disease, and Down syndrome. In this review we summarize the mechanisms by which MIR155HG expression can be regulated. Given that the pathologies mediated by miR-155-5p result from the over-expression of this miRNA it may be possible to therapeutically attenuate miR-155-5p levels in the treatment of several pathological processes. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:1 / 12
页数:12
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