2 FK506 RESISTANCE-CONFERRING GENES IN SACCHAROMYCES-CEREVISIAE, TAT1 AND TAT2, ENCODE AMINO-ACID PERMEASES MEDIATING TYROSINE AND TRYPTOPHAN UPTAKE

被引:139
作者
SCHMIDT, A [1 ]
HALL, MN [1 ]
KOLLER, A [1 ]
机构
[1] UNIV BASEL, BIOCTR, DEPT BIOCHEM, CH-4056 BASEL, SWITZERLAND
关键词
D O I
10.1128/MCB.14.10.6597
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
The macrocyclic lactone FK506 exerts immunosuppressive effects on T lymphocytes by interfering with signal transduction leading to T-cell activation and also inhibits the growth of eukaryotic microorganisms, including Saccharomyces cerevisiae. We reported previously that an FK506-sensitive target in S. cerevisiae is required for amino acid import and that overexpression of two new genes, TAT1 and TAT2 (formerly called TAP1 and TAP2), confers resistance to the drug. Here we report that TAT1 and TAT2 encode novel members of the yeast amino acid permease family composed of integral membrane proteins that share 30 to 40% identity. TAT1 is the tyrosine high-affinity transporter, which also mediates low-affinity or low-capacity uptake of tryptophan. TAT2 is the tryptophan high-affinity transporter. PK506 does not reduce the levels of TAT1 and TAT2 transcripts, indicating that the inhibition of amino acid transport by the drug is posttranscriptional.
引用
收藏
页码:6597 / 6606
页数:10
相关论文
共 48 条
[31]  
MAGASANIK B, 1993, MOL BIOL YEAST SACCH, P283
[32]   MUTATIONS IN SACCHAROMYCES-CEREVISIAE WHICH CONFER RESISTANCE TO SEVERAL AMINO-ACID-ANALOGS [J].
MCCUSKER, JH ;
HABER, JE .
MOLECULAR AND CELLULAR BIOLOGY, 1990, 10 (06) :2941-2949
[33]   ACTION OF TRYPTOPHAN ANALOGS IN SACCHAROMYCES-CEREVISIAE [J].
MIOZZARI, G ;
NIEDERBERGER, P ;
HUTTER, R .
ARCHIVES OF MICROBIOLOGY, 1977, 115 (03) :307-316
[34]  
MOSCH HU, 1991, J BIOL CHEM, V266, P20452
[35]   THE COMPLETE DNA-SEQUENCE OF YEAST CHROMOSOME-III [J].
OLIVER, SG ;
VANDERAART, QJM ;
AGOSTONI-CARBONE, ML ;
AIGLE, M ;
ALBERGHINA, L ;
ALEXANDRAKI, D ;
ANTOINE, G ;
ANWAR, R ;
BALLESTA, JPG ;
BENIT, P ;
BERBEN, G ;
BERGANTINO, E ;
BITEAU, N ;
BOLLE, PA ;
BOLOTINFUKUHARA, M ;
BROWN, A ;
BROWN, AJP ;
BUHLER, JM ;
CARCANO, C ;
CARIGNANI, G ;
CEDERBERG, H ;
CHANET, R ;
CONTRERAS, R ;
CROUZET, M ;
DAIGNANFORNIER, B ;
DEFOOR, E ;
DELGADO, M ;
DEMOLDER, J ;
DOIRA, C ;
DUBOIS, E ;
DUJON, B ;
DUSTERHOFT, A ;
ERDMANN, D ;
ESTEBAN, M ;
FABRE, F ;
FAIRHEAD, C ;
FAYE, G ;
FELDMANN, H ;
FIERS, W ;
FRANCINGUESGAILLARD, MC ;
FRANCO, L ;
FRONTALI, L ;
FUKUHARA, H ;
FULLER, LJ ;
GALLAND, P ;
GENT, ME ;
GIGOT, D ;
GILLIQUET, V ;
GLANSDORFF, N ;
GOFFEAU, A .
NATURE, 1992, 357 (6373) :38-46
[36]  
PHILIPPSEN P, 1991, METHOD ENZYMOL, V194, P169
[37]  
Sambrook J., 1989, MOL CLONING LAB MANU
[38]   DNA SEQUENCING WITH CHAIN-TERMINATING INHIBITORS [J].
SANGER, F ;
NICKLEN, S ;
COULSON, AR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1977, 74 (12) :5463-5467
[39]   CHEMISTRY AND BIOLOGY OF THE IMMUNOPHILINS AND THEIR IMMUNOSUPPRESSIVE LIGANDS [J].
SCHREIBER, SL .
SCIENCE, 1991, 251 (4991) :283-287
[40]  
SHERMAN F, 1991, METHOD ENZYMOL, V194, P3