Box C/D Small Nucleolar RNA (snoRNA) U60 Regulates Intracellular Cholesterol Trafficking

被引:43
作者
Brandis, Katrina A. [1 ]
Gale, Sarah [1 ]
Jinn, Sarah [1 ]
Langmade, Stephen J. [1 ]
Dudley-Rucker, Nicole [1 ]
Jiang, Hui [1 ]
Sidhu, Rohini [1 ]
Ren, Aileen [1 ]
Goldberg, Anna [1 ]
Schaffer, Jean E. [1 ]
Ory, Daniel S. [1 ]
机构
[1] Washington Univ, Sch Med, Diabet Cardiovasc Dis Ctr, St Louis, MO 63110 USA
基金
美国国家卫生研究院;
关键词
Cholesterol; Cholesterol Regulation; Intracellular Trafficking; Lipid Transport; Small Nucleolar RNA (snoRNA); Noncoding RNA; ENDOPLASMIC-RETICULUM CHOLESTEROL; PLASMA-MEMBRANE; STEROL TRANSPORT; ACCESSIBILITY; HOMEOSTASIS; SCREEN; MIR-33; GENES; CELLS; ER;
D O I
10.1074/jbc.M113.488577
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
Background: The mechanisms regulating internalization of plasma membrane cholesterol in mammalian cells are not well understood. Results: A cell line haploinsufficient for U60 snoRNA expression exhibits impaired plasma membrane to ER cholesterol trafficking and increased de novo cholesterol synthesis. Conclusion: U60 snoRNA expression regulates cholesterol homeostasis by affecting internalization of plasma membrane cholesterol. Significance: This is the first study to implicate a snoRNA in regulation of cholesterol homeostasis. Mobilization of plasma membrane (PM) cholesterol to the endoplasmic reticulum is essential for cellular cholesterol homeostasis. The mechanisms regulating this retrograde, intermembrane cholesterol transfer are not well understood. Because mutant cells with defects in PM to endoplasmic reticulum cholesterol trafficking can be isolated on the basis of resistance to amphotericin B, we conducted an amphotericin B loss-of-function screen in Chinese hamster ovary (CHO) cells using insertional mutagenesis to identify genes that regulate this trafficking mechanism. Mutant line A1 displayed reduced cholesteryl ester formation from PM-derived cholesterol and increased de novo cholesterol synthesis, indicating a deficiency in retrograde cholesterol transport. Genotypic analysis revealed that the A1 cell line contained one disrupted allele of the U60 small nucleolar RNA (snoRNA) host gene, resulting in haploinsufficiency of the box C/D snoRNA U60. Complementation and mutational studies revealed the U60 snoRNA to be the essential feature from this locus that affects cholesterol trafficking. Lack of alteration in predicted U60-mediated site-directed methylation of 28 S rRNA in the A1 mutant suggests that the U60 snoRNA modulates cholesterol trafficking by a mechanism that is independent of this canonical function. Our study adds to a growing body of evidence for participation of small noncoding RNAs in cholesterol homeostasis and is the first to implicate a snoRNA in this cellular function.
引用
收藏
页码:35703 / 35713
页数:11
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