Vacuolar Import of Phosphatidylcholine Requires the ATP-Binding Cassette Transporter Ybt1

被引:29
作者
Gulshan, Kailash [1 ]
Moye-Rowley, W. Scott [1 ]
机构
[1] Univ Iowa, Dept Mol Physiol & Biophys, Carver Coll Med, Iowa City, IA 52246 USA
关键词
ABC transporter; biosynthesis; NBD-PC; phosphatidycholine; vacuole; NBD-LABELED PHOSPHATIDYLCHOLINE; RESISTANCE-ASSOCIATED PROTEIN; YEAST PLASMA-MEMBRANE; SACCHAROMYCES-CEREVISIAE; ABC TRANSPORTER; AMINOPHOSPHOLIPID TRANSLOCASE; METAL RESISTANCE; CYSTIC-FIBROSIS; PHOSPHATIDYLETHANOLAMINE; MRP;
D O I
10.1111/j.1600-0854.2011.01228.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
ATP-binding cassette (ABC) transporters are well known for their roles as multidrug resistance determinants but also play important roles in regulation of lipid levels. In the yeast Saccharomyces cerevisiae, the plasma membrane ABC transporter proteins Pdr5 and Yor1 are required for normal rates of transport of phosphatidyethanolamine to the surface of the cell. Loss of these ABC transporters causes a defect in phospholipid asymmetry across the plasma membrane and has been linked with slowed rates of trafficking of othermembrane proteins. Four ABC transporter proteins are found on the limiting membrane of the yeast vacuole and loss of one of these vacuolar ABC transporters, Ybt1, caused a major defect in the normal delivery of the phosphatidylcholine ( PC) analog NBD-PC (7-nitro-2,1,3-benzoxadiazol-PC) to the lumen of the vacuole. NBD-PC accumulates on cytosolic membranes in an ybt1 Delta strain. We demonstrated that Ybt1 is required to import NBD-PC into vacuoles in the presence of ATP in vitro. Loss of Ybt1 prevented vacuolar remodeling of PC analogs. Turnover of Ybt1 was reduced under conditions in which function of this vacuolar remodeling pathway was required. Our data describe a novel vacuolar route for lipid remodeling and reutilization in addition to previously described enzymatic avenues in the cytoplasm.
引用
收藏
页码:1257 / 1268
页数:12
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