SUR1 (CSG1/BCL21), a gene necessary for growth of Saccharomyces cerevisiae in the presence of high Ca2+ concentrations at 37 degrees C, is required for mannosylation of inositolphosphorylceramide

被引:118
作者
Beeler, TJ [1 ]
Fu, D [1 ]
Rivera, J [1 ]
Monaghan, E [1 ]
Gable, K [1 ]
Dunn, TM [1 ]
机构
[1] UNIFORMED SERV UNIV HLTH SCI,DEPT BIOCHEM,BETHESDA,MD 20814
来源
MOLECULAR & GENERAL GENETICS | 1997年 / 255卷 / 06期
关键词
Saccharomyces cerevisiae; calcium; copper; sphingolipid; CSG1;
D O I
10.1007/s004380050530
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
Saccharomyces cerevisiae cells require two genes, CSG1/SUR1 and CSG2, for growth in 50 mM Ca2+, but not 50 mM Sr2+. CSG2 was previously shown to be required for the mannosylation of inositol-phosphorylceramide (IPC) to form mannosylinositolphosphorylceramide (MIPC). Here we demonstrate that SUR1/CSG1 is both genetically and biochemically related to CSG2. Like CSG2, SUR1/CSG1 is required for IPC mannosylation. A 93-amino acid stretch of Csg1p shows 29% identity with the alpha-1, 6-mannosyltransferase encoded by OCH1. The SUR1/CSG1 gene is a dose-dependent suppressor of the Ca2+-sensitive phenotype of the csg2 mutant, but overexpression of CSG2 does not suppress the Ca2+ sensitivity of the csg1 mutant. The csg1 and csg2 mutants display normal growth in YPD, indicating that mannosylation elf sphingolipids is not essential.]Increased osmolarity of the growth medium increases the Ca2+ tolerance of csg1 and csg2 mutant cells suggesting that altered cell wall synthesis causes Ca2+-induced death. Hydroxylation of IPC-C to form IPC-D requires CCC2, a gene encoding an intracellular cellular Cu transporter. Increased expression of CCC2 or increased Cu2+ concentration in the growth medium enhances the Ca2+ tolerance of csg1 mutants, suggesting that accumulation of IPC-C renders csg1 cells Ca2+ sensitive.
引用
收藏
页码:570 / 579
页数:10
相关论文
共 35 条
[1]   GUANOSINE DIPHOSPHATASE IS REQUIRED FOR PROTEIN AND SPHINGOLIPID GLYCOSYLATION IN THE GOLGI LUMEN OF SACCHAROMYCES-CEREVISIAE [J].
ABEIJON, C ;
YANAGISAWA, K ;
MANDON, EC ;
HAUSLER, A ;
MOREMEN, K ;
HIRSCHBERG, CB ;
ROBBINS, PW .
JOURNAL OF CELL BIOLOGY, 1993, 122 (02) :307-323
[2]   SEQUENCE-ANALYSIS OF A 5.6-KB FRAGMENT OF CHROMOSOME-II FROM SACCHAROMYCES-CEREVISIAE REVEALS 2 NEW OPEN READING FRAMES NEXT TO CDC28 [J].
BAUR, S ;
BECKER, J ;
LI, ZY ;
NIEGEMANN, E ;
WEHNER, E ;
WOLTER, R ;
BRENDEL, M .
YEAST, 1995, 11 (05) :455-458
[3]  
BEELER T, 1994, J BIOL CHEM, V269, P7279
[4]  
BOEKE JD, 1987, METHOD ENZYMOL, V154, P164
[5]   MOLECULAR-BASIS OF CELL INTEGRITY AND MORPHOGENESIS IN SACCHAROMYCES-CEREVISIAE [J].
CID, VJ ;
DURAN, A ;
DELREY, F ;
SNYDER, MP ;
NOMBELA, C ;
SANCHEZ, M .
MICROBIOLOGICAL REVIEWS, 1995, 59 (03) :345-386
[6]   YEAST MUTANT AFFECTED FOR VIABILITY UPON NUTRIENT STARVATION - CHARACTERIZATION AND CLONING OF THE RVS161 GENE [J].
CROUZET, M ;
URDACI, M ;
DULAU, L ;
AIGLE, M .
YEAST, 1991, 7 (07) :727-743
[7]  
Cunningham KW, 1996, MOL CELL BIOL, V16, P2226
[8]  
Danks DM, 1989, METABOLIC BASIS INHE, P1411
[9]  
DAVIS TN, 1995, ADV SEC MESS PHOSPH, V30, P339
[10]   YEAST MUTANTS AFFECTED IN VIABILITY UPON STARVATION HAVE A MODIFIED PHOSPHOLIPID-COMPOSITION [J].
DESFARGES, L ;
DURRENS, P ;
JUGUELIN, H ;
CASSAGNE, C ;
BONNEU, M ;
AIGLE, M .
YEAST, 1993, 9 (03) :267-277