ABCA1
甾醇调节元件结合蛋白
生物
胆固醇
心理压抑
小RNA
调节器
基因
RNA干扰
细胞生物学
甾醇
ATP结合盒传送带1
转录因子
生物化学
基因表达
核糖核酸
运输机
作者
S. Hani Najafi‐Shoushtari,Fjoralba Kristo,Yingxia Li,Toshi Shioda,David E. Cohen,Robert E. Gerszten,Anders M. Näär
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2010-05-13
卷期号:328 (5985): 1566-1569
被引量:923
标识
DOI:10.1126/science.1189123
摘要
miR-33 in Cholesterol Control With the well-established link between serum cholesterol levels and cardiovascular disease and the availability of effective cholesterol-lowering drugs, cholesterol screening has rapidly become a routine part of health care. Yet, much remains to be learned about how cholesterol levels are regulated at the cellular level (see the Perspective by Brown et al. ). Now, Najafi-Shoushtari et al. (p. 1566 , published online 13 May) and Rayner et al. (p. 1570 , published online 13 May) have discovered a new molecular player in cholesterol control—a small noncoding RNA that, intriguingly, is embedded within the genes coding for sterol regulatory element-binding proteins (SREBPs), transcription factors already known to regulate cholesterol levels. This microRNA, called miR-33, represses expression of the adenosine triphosphate–binding cassette transporter A1, a protein that regulates synthesis of high-density lipoprotein (HDL, or “good” cholesterol) and that helps to remove “bad” cholesterol from the blood. Reducing the levels of miR-33 in mice boosted serum HDL levels, suggesting that manipulation of this regulatory circuit might be therapeutically useful.
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