Increase in cellular triacylglycerol content and emergence of large ER-associated lipid droplets in the absence of CDP-DG synthase function

被引:13
|
作者
He, Yue [1 ,2 ]
Yam, Candice [1 ,2 ]
Pomraning, Kyle [3 ]
Chin, Jacqueline S. R. [1 ,2 ]
Yew, Joanne Y. [1 ,2 ]
Freitag, Michael [3 ]
Oliferenko, Snezhana [2 ,4 ]
机构
[1] Temasek Life Sci Lab, Singapore 117604, Singapore
[2] Natl Univ Singapore, Dept Biol Sci, Singapore 117543, Singapore
[3] Oregon State Univ, Dept Biochem & Biophys, Corvallis, OR USA
[4] Kings Coll London, Randall Div Cell & Mol Biophys, London SE1 1UL, England
基金
新加坡国家研究基金会; 美国国家卫生研究院; 美国国家科学基金会;
关键词
YEAST SACCHAROMYCES-CEREVISIAE; SCHIZOSACCHAROMYCES-POMBE; FISSION YEAST; ESCHERICHIA-COLI; DIACYLGLYCEROL SYNTHASE; PHOSPHATIDIC-ACID; DIGLYCERIDE SYNTHETASE; ENDOPLASMIC-RETICULUM; JAPONICUS; GENE;
D O I
10.1091/mbc.E14-03-0832
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Excess fatty acids and sterols are stored as triacylglycerols and sterol esters in specialized cellular organelles, called lipid droplets. Understanding what determines the cellular amount of neutral lipids and their packaging into lipid droplets is of fundamental and applied interest. Using two species of fission yeast, we show that cycling cells deficient in the function of the ER-resident CDP-DG synthase Cds1 exhibit markedly increased triacylglycerol content and assemble large lipid droplets closely associated with the ER membranes. We demonstrate that these unusual structures recruit the triacylglycerol synthesis machinery and grow by expansion rather than by fusion. Our results suggest that interfering with the CDP-DG route of phosphatidic acid utilization rewires cellular metabolism to adopt a triacylglycerol-rich lifestyle reliant on the Kennedy pathway.
引用
收藏
页码:4083 / 4095
页数:13
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