Interactions of the F-1-ATPase subunits from Escherichia coli detected by the yeast two-hybrid system

被引:9
作者
Moritani, C [1 ]
Sawada, K [1 ]
Takemoto, K [1 ]
Shin, YC [1 ]
Nemoto, S [1 ]
Noumi, T [1 ]
Kanazawa, H [1 ]
机构
[1] OKAYAMA UNIV, FAC ENGN SCI, DEPT BIOTECHNOL, OKAYAMA 700, JAPAN
来源
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS | 1996年 / 1274卷 / 1-2期
关键词
ATPase; F-1; subunit interaction; two-hybrid system;
D O I
10.1016/0005-2728(96)00013-8
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
Subunit interactions among the F-1-ATPase subunits were studied by the yeast two-hybrid system. Various pairwise combinations of genes encoding alpha, beta, gamma, delta and epsilon subunits of Escherichia coli H+-ATPase fused to the DNA-binding or activation domain of the yeast GAL4 gene were introduced into yeast and expression of a reporter gene encoding beta-galactosidase was detected. Combinations of the alpha and beta subunit genes, and of the epsilon and gamma subunit genes showed high levels of reporter gene expression, while those of alpha and delta, beta and delta, gamma and delta, and delta and epsilon demonstrated weak but significant reporter gene expression. However, combinations of alpha and gamma, beta and gamma, and epsilon, and beta and epsilon did not induce reporter gene expression. None of the fused genes alone induced reporter gene expression. These results suggested that specific and strong interactions between the alpha and beta, gamma and epsilon, and weak interactions between the alpha and delta, beta and delta, and gamma and delta subunits occurred in yeast cells in the two-hybrid system. Effects of previouly identified mutant beta subunits with Leu-40 to Pro, Glu-41 to Lys or Pro-332 to Gin subsitutions which caused defects in molecular assembly of F-1-ATPase were analyzed with regard to alpha-beta interaction. No interaction of the alpha and beta subunits was observed in this system using the beta subunit with mutation of Pro-332 to Gin. However, for the other two mutations, alpha-beta interactions were observed. This system may be useful for isolating mutants which have defects in interaction of F-1-ATPase subunits.
引用
收藏
页码:67 / 72
页数:6
相关论文
共 40 条
[1]   STRUCTURE AT 2.8-ANGSTROM RESOLUTION OF F1-ATPASE FROM BOVINE HEART-MITOCHONDRIA [J].
ABRAHAMS, JP ;
LESLIE, AGW ;
LUTTER, R ;
WALKER, JE .
NATURE, 1994, 370 (6491) :621-628
[2]   INTRODUCTION OF REACTIVE CYSTEINE RESIDUES IN THE EPSILON-SUBUNIT OF ESCHERICHIA-COLI F1 ATPASE, MODIFICATION OF THESE SITES WITH TETRAFLUOROPHENYL AZIDE MALEIMIDES, AND EXAMINATION OF CHANGES IN THE BINDING OF THE EPSILON-SUBUNIT WHEN DIFFERENT NUCLEOTIDES ARE IN CATALYTIC SITES [J].
AGGELER, R ;
CHICASCRUZ, K ;
CAI, SX ;
KEANA, JFW ;
CAPALDI, RA .
BIOCHEMISTRY, 1992, 31 (11) :2956-2961
[3]  
ARIS JP, 1983, J BIOL CHEM, V258, P4599
[4]   COUPLING BETWEEN CATALYTIC SITES AND THE PROTON CHANNEL IN F1F0-TYPE ATPASES [J].
CAPALDI, RA ;
AGGELER, R ;
TURINA, P ;
WILKENS, S .
TRENDS IN BIOCHEMICAL SCIENCES, 1994, 19 (07) :284-289
[5]   PROTEIN-INTERACTION CLONING IN YEAST - IDENTIFICATION OF MAMMALIAN PROTEINS THAT REACT WITH THE LEUCINE ZIPPER OF JUN [J].
CHEVRAY, PM ;
NATHANS, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (13) :5789-5793
[6]  
DALLMANN HG, 1992, J BIOL CHEM, V267, P18953
[7]  
DUNN SD, 1980, J BIOL CHEM, V255, P113
[8]  
DUNN SD, 1982, J BIOL CHEM, V257, P7354
[9]   A NOVEL GENETIC SYSTEM TO DETECT PROTEIN PROTEIN INTERACTIONS [J].
FIELDS, S ;
SONG, OK .
NATURE, 1989, 340 (6230) :245-246
[10]  
Fillingame R.H., 1990, BACTERIA TREATISE ST, V12, P345