Phenotypic effects of membrane protein overexpression in Saccharomyces cerevisiae

被引:28
作者
Osterberg, Marie
Kim, Hyun
Warringer, Jonas
Melen, Karin
Blomberg, Anders
von Heijne, Gunnar [1 ]
机构
[1] Stockholm Univ, Ctr Biomembrane Res, Dept Biochem & Biophys, SE-10691 Stockholm, Sweden
[2] AlbaNova, Stockholm Bioinformat Ctr, SE-10691 Stockholm, Sweden
[3] Univ Gothenburg, Dept Cell & Mol Biol, SE-41390 Gothenburg, Sweden
关键词
caffeine; paraquat; salt tolerance; yeast;
D O I
10.1073/pnas.0604078103
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Large-scale protein overexpression phenotype screens provide an important complement to the more common gene knockout screens. Here, we have targeted the so far poorly understood Saccharomyces cerevisiae membrane proteome and report growth phenotypes for a strain collection overexpressing approximate to 600 C-terminally tagged integral membrane proteins grown both under normal and three different stress conditions. Although overexpression of most membrane proteins reduce the growth rate in synthetic defined medium, we identify a large number of proteins that, when overexpressed, confer specific resistance to various stress conditions. Our data suggest that regulation of glycosylphosphatidylinositol anchor biosynthesis and the Na+/K+ homeostasis system constitute major downstream targets of the yeast PKA/RAS pathway and point to a possible connection between the early secretory pathway and the cells' response to oxidative stress. We also have quantified the expression levels for > 550 membrane proteins, facilitating the choice of well expressing proteins for future functional and structural studies.
引用
收藏
页码:11148 / 11153
页数:6
相关论文
共 54 条
[1]  
Bateman A, 2004, NUCLEIC ACIDS RES, V32, pD138, DOI [10.1093/nar/gkp985, 10.1093/nar/gkr1065, 10.1093/nar/gkh121]
[2]   POTASSIUM REQUIREMENTS OF SACCHAROMYCES-CEREVISIAE [J].
CAMACHO, M ;
RAMOS, J ;
RODRIGUEZNAVARRO, A .
CURRENT MICROBIOLOGY, 1981, 6 (05) :295-299
[3]   Differential trafficking and timed localization of two chitin synthase proteins, Chs2p and Chs3p [J].
Chuang, JS ;
Schekman, RW .
JOURNAL OF CELL BIOLOGY, 1996, 135 (03) :597-610
[4]   Global topology analysis of the Escherichia coli inner membrane proteome [J].
Daley, DO ;
Rapp, M ;
Granseth, E ;
Melén, K ;
Drew, D ;
von Heijne, G .
SCIENCE, 2005, 308 (5726) :1321-1323
[5]   Membrane topology and function of Der3/Hrd1p as a ubiquitin-protein ligase (E3) involved in endoplasmic reticulum degradation [J].
Deak, PM ;
Wolf, DH .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (14) :10663-10669
[6]   Synthesis of mannose-(inositol-P)(2)-ceramide, the major sphingolipid in Saccharomyces cerevisiae, requires the IPT1 (YDR072c) gene [J].
Dickson, RC ;
Nagiec, EE ;
Wells, GB ;
Nagiec, MM ;
Lester, RL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (47) :29620-29625
[7]  
Ehrenhofer-Murray AE, 1998, YEAST, V14, P49, DOI 10.1002/(SICI)1097-0061(19980115)14:1<49::AID-YEA199>3.0.CO
[8]  
2-T
[9]   Cluster analysis and display of genome-wide expression patterns [J].
Eisen, MB ;
Spellman, PT ;
Brown, PO ;
Botstein, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (25) :14863-14868
[10]   HOL1 MUTATIONS CONFER NOVEL ION-TRANSPORT IN SACCHAROMYCES-CEREVISIAE [J].
GABER, RF ;
KIELLANDBRANDT, MC ;
FINK, GR .
MOLECULAR AND CELLULAR BIOLOGY, 1990, 10 (02) :643-652