Post-transcriptional regulation in metabolic diseases

被引:27
作者
Kim, Wook [2 ]
Lee, Eun Kyung [1 ]
机构
[1] Catholic Univ Korea, Dept Chem, Coll Med, Seoul, South Korea
[2] NIA, Lab Clin Invest, Intramural Res Program, NIH, Baltimore, MD 21224 USA
基金
新加坡国家研究基金会;
关键词
post-transcriptional gene regulation; microRNAs; RNA-binding proteins; glucose homeostasis; lipid homeostasis; diabetes; metabolic disease; PANCREATIC BETA-CELLS; MESENCHYMAL STEM-CELLS; RNA-BINDING PROTEINS; ADIPOGENIC DIFFERENTIATION; INSULIN-RESISTANCE; MESSENGER-RNA; ADIPOCYTE DIFFERENTIATION; DIABETES-MELLITUS; LIPID-METABOLISM; ADIPOSE-TISSUE;
D O I
10.4161/rna.20091
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
Post-transcriptional gene regulation by microRNAs (miRNAs) and RNA-binding proteins (RBPs) is central to many biological functions. Aberrant gene expression patterns underlie many metabolic diseases that represent major public health concerns and formidable therapeutic challenges. Several studies have established a number of post-transcriptional regulators implicated in metabolic diseases such as diabetes and obesity. In addition, emerging knowledge of metabolically active and insulin-sensitive organs, such as the pancreas, liver, muscle and adipose compartment, is rapidly expanding the panel of potential therapeutic targets for the treatment of metabolic diseases. Here, we review our current understanding of miRNAs and RBPs that affect glucose and lipid homeostasis, and their roles in normal physiology and metabolic disorders, especially type 2 diabetes and obesity.
引用
收藏
页码:772 / 780
页数:9
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