Suppressor gene analysis reveals an essential role for sphingolipids in transport of glycosylphosphatidylinositol-anchored proteins in Saccharomyces cerevisiae

被引:70
作者
Skrzypek, M
Lester, RL
Dickson, RC
机构
[1] UNIV KENTUCKY, MED CTR, DEPT BIOCHEM, LEXINGTON, KY 40536 USA
[2] UNIV KENTUCKY, MED CTR, LUCILLE P MARKEY CANC CTR, LEXINGTON, KY 40536 USA
关键词
D O I
10.1128/jb.179.5.1513-1520.1997
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Sphingolipids are normally necessary for growth of Saccharomyces cerevisiae cells, but mutant strains that bypass the need for sphingolipids have been identified. Such bypass mutants fail to grow under stressful conditions, including low pH (pH 4.1), when they lack sphingolipids. To begin to understand why sphingolipids seem to be necessary for coping with low-pH stress, we screened a genomic library and selected a suppressor gene, CWP2 (cell wall protein 2), that when present in multiple copies partially compensates for the lack of sphingolipids and enhances survival at low pH. To explain these results, we present evidence that sphingolipids are required for a normal rate of transport of glycosylphosphatidylinositol (GPI)-anchored proteins, including Cwp2 and Gas1/Gpg1, from the endoplasmic reticulum (ER) to the Golgi apparatus. The effect of sphingolipids is specific for transport of GPI-anchored proteins because no effect on the rate of transport of carboxypeptidase Y, a non-GPI-anchored protein, was observed. Since the Gas1 protein accumulated in the ER with a GPI anchor in cells lacking sphingolipids, we conclude that sphingolipids are not necessary for anchor attachment. Therefore, sphingolipids must be necessary for a step in formation of COPII vesicles or for their transport to the Golgi apparatus. Our data identify the Cwp2 protein asa vital component in protecting cells from the stress of low pH.
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页码:1513 / 1520
页数:8
相关论文
共 52 条
[31]   GLYCOSYL PHOSPHATIDYLINOSITOL-DEPENDENT CROSS-LINKING OF ALPHA-AGGLUTININ AND BETA-1,6-GLUCAN IN THE SACCHAROMYCES-CEREVISIAE CELL-WALL [J].
LU, CF ;
MONTIJN, RC ;
BROWN, JL ;
KLIS, F ;
KURJAN, J ;
BUSSEY, H ;
LIPKE, PN .
JOURNAL OF CELL BIOLOGY, 1995, 128 (03) :333-340
[32]   THE SIGNAL MODULATOR PROTEIN-14-3-3 TS A TARGET OF SPHINGOSINE-DEPENDENT OR N,N-DIMETHYLSPHINGOSINE-DEPENDENT KINASE IN 3T3(A31) CELLS [J].
MEGIDISH, T ;
WHITE, T ;
TAKIO, K ;
TITANI, K ;
IGARASHI, Y ;
HAKOMORI, S .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1995, 216 (03) :739-747
[33]  
MERRILL AH, 1991, J BIOENERG BIOMEMBR, V23, P83
[34]   THE LCB2 GENE OF SACCHAROMYCES AND THE RELATED LCB1 GENE ENCODE SUBUNITS OF SERINE PALMITOYLTRANSFERASE, THE INITIAL ENZYME IN SPHINGOLIPID SYNTHESIS [J].
NAGIEC, MM ;
BALTISBERGER, JA ;
WELLS, GB ;
LESTER, RL ;
DICKSON, RC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (17) :7899-7902
[35]  
NAGIEC MM, 1993, J BIOL CHEM, V268, P22156
[36]   DETERMINANTS FOR GLYCOPHOSPHOLIPID ANCHORING OF THE SACCHAROMYCES-CEREVISIAE GAS1 PROTEIN TO THE PLASMA-MEMBRANE [J].
NUOFFER, C ;
JENO, P ;
CONZELMANN, A ;
RIEZMAN, H .
MOLECULAR AND CELLULAR BIOLOGY, 1991, 11 (01) :27-37
[37]   SPHINGOSINE-1-PHOSPHATE AS 2ND MESSENGER IN CELL-PROLIFERATION INDUCED BY PDGF AND FCS MITOGENS [J].
OLIVERA, A ;
SPIEGEL, S .
NATURE, 1993, 365 (6446) :557-560
[38]   PHENOTYPES OF SPHINGOLIPID-DEPENDENT STRAINS OF SACCHAROMYCES-CEREVISIAE [J].
PATTON, JL ;
SRINIVASAN, B ;
DICKSON, RC ;
LESTER, RL .
JOURNAL OF BACTERIOLOGY, 1992, 174 (22) :7180-7184
[39]   SPHINGOLIPID LONG-CHAIN-BASE AUXOTROPHS OF SACCHAROMYCES-CEREVISIAE - GENETICS, PHYSIOLOGY, AND A METHOD FOR THEIR SELECTION [J].
PINTO, WJ ;
SRINIVASAN, B ;
SHEPHERD, S ;
SCHMIDT, A ;
DICKSON, RC ;
LESTER, RL .
JOURNAL OF BACTERIOLOGY, 1992, 174 (08) :2565-2574
[40]   PHYSIOLOGICAL ANALYSIS OF MUTANTS INDICATES INVOLVEMENT OF THE SACCHAROMYCES-CEREVISIAE GPI-ANCHORED PROTEIN GP115 IN MORPHOGENESIS AND CELL-SEPARATION [J].
POPOLO, L ;
VAI, M ;
GATTI, E ;
PORELLO, S ;
BONFANTE, P ;
BALESTRINI, R ;
ALBERGHINA, L .
JOURNAL OF BACTERIOLOGY, 1993, 175 (07) :1879-1885