A block in endoplasmic reticulum-to-golgi trafficking inhibits phospholipid synthesis and induces neutral lipid accumulation

被引:56
作者
Gaspar, Maria L. [1 ]
Jesch, Stephen A. [1 ]
Viswanatha, Raghuvir [1 ]
Antosh, Amy L. [1 ]
Brown, William J. [1 ]
Kohlwein, Sepp D. [2 ]
Henry, Susan A. [1 ]
机构
[1] Cornell Univ, Dept Mol Biol & Genet, Ithaca, NY 14853 USA
[2] Graz Univ, Inst Mol Biosci, A-8010 Graz, Austria
基金
奥地利科学基金会; 美国国家卫生研究院;
关键词
D O I
10.1074/jbc.M802685200
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
Seeking to better understand how membrane trafficking is coordinated with phospholipid synthesis in yeast, we investigated lipid synthesis in several Sec(-) temperature-sensitive mutants, including sec13-1. Upon shift of sec13-1 cells to the restrictive temperature of 37 degrees C, phospholipid synthesis decreased dramatically relative to the wild type control, whereas synthesis of neutral lipids, especially triacylglycerol ( TAG), increased. When examined by fluorescence microscopy, the number of lipid droplets appeared to increase and formed aggregates in sec13-1 cells shifted to 37 degrees C. Electron microscopy confirmed the increase in lipid droplet number and revealed that many were associated with the vacuole. Analysis of lipid metabolism in strains lacking TAG synthase genes demonstrated that the activities of the products of these genes contribute to accumulation of TAG in sec13-1 cells after the shift to 37 degrees C. Furthermore, the permissive temperature for growth of the sec13-1 strain lacking TAG synthase genes was 3 degrees C lower than sec13-1 on several different growth media, indicating that the synthesis of TAG has physiological significance under conditions of secretory stress. Together these results suggest that following a block in membrane trafficking, yeast cells channel lipid metabolism from phospholipid synthesis into synthesis of TAG and other neutral lipids to form lipid droplets. We conclude that this metabolic switch provides a degree of protection to cells during secretory stress.
引用
收藏
页码:25735 / 25751
页数:17
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共 70 条
[51]   SEC31 encodes an essential component of the COPII coat required for transport vesicle budding from the endoplasmic reticulum [J].
Salama, NR ;
Chuang, JS ;
Schekman, RW .
MOLECULAR BIOLOGY OF THE CELL, 1997, 8 (02) :205-217
[52]   THE SEC13P COMPLEX AND RECONSTITUTION OF VESICLE BUDDING FROM THE ER WITH PURIFIED CYTOSOLIC PROTEINS [J].
SALAMA, NR ;
YEUNG, T ;
SCHEKMAN, RW .
EMBO JOURNAL, 1993, 12 (11) :4073-4082
[53]   Storage lipid synthesis is non-essential in yeast [J].
Sandager, L ;
Gustavsson, MH ;
Ståhl, U ;
Dahlqvist, A ;
Wiberg, E ;
Banas, A ;
Lenman, M ;
Ronne, H ;
Stymne, S .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (08) :6478-6482
[54]   ERD2, A YEAST GENE REQUIRED FOR THE RECEPTOR-MEDIATED RETRIEVAL OF LUMINAL ER PROTEINS FROM THE SECRETORY PATHWAY [J].
SEMENZA, JC ;
HARDWICK, KG ;
DEAN, N ;
PELHAM, HRB .
CELL, 1990, 61 (07) :1349-1357
[55]   A novel complex of nucleoporins, which includes Sec13p and a Sec13p homolog, is essential for normal nuclear pores [J].
Siniossoglou, S ;
Wimmer, C ;
Rieger, M ;
Doye, V ;
Tekotte, H ;
Weise, C ;
Emig, S ;
Segref, A ;
Hurt, EC .
CELL, 1996, 84 (02) :265-275
[56]   Structure and assembly of the Nup84p complex [J].
Siniossoglou, S ;
Lutzmann, M ;
Santos-Rosa, H ;
Leonard, K ;
Mueller, S ;
Aebi, U ;
Hurt, E .
JOURNAL OF CELL BIOLOGY, 2000, 149 (01) :41-53
[57]   XBP1: a link between the unfolded protein response, lipid biosynthesis, and biogenesis of the endoplasmic reticulum [J].
Sriburi, R ;
Jackowski, S ;
Mori, K ;
Brewer, JW .
JOURNAL OF CELL BIOLOGY, 2004, 167 (01) :35-41
[58]   Coordinate regulation of phospholipid biosynthesis and secretory pathway gene expression in XBP-1 (S)-induced endoplasmic reticulum biogenesis [J].
Sriburi, Rungtawan ;
Bommiasamy, Hemamalini ;
Buldak, Gerald L. ;
Robbins, Gregory R. ;
Frank, Matthew ;
Jackowski, Suzanne ;
Brewer, Joseph W. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2007, 282 (10) :7024-7034
[59]   EARLY STAGES IN THE YEAST SECRETORY PATHWAY ARE REQUIRED FOR TRANSPORT OF CARBOXYPEPTIDASE-Y TO THE VACUOLE [J].
STEVENS, T ;
ESMON, B ;
SCHEKMAN, R .
CELL, 1982, 30 (02) :439-448
[60]   The lipodystrophy protein seipin is found at endoplasmic reticulum lipid droplet junctions and is important for droplet morphology [J].
Szymanski, Kimberly M. ;
Binns, Derk ;
Bartz, Ren ;
Grishin, Nick V. ;
Li, Wei-Ping ;
Agarwal, Anil K. ;
Garg, Abhimanyu ;
Anderson, Richard G. W. ;
Goodman, Joel M. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2007, 104 (52) :20890-20895