PLEIOTROPIC FUNCTION OF ARGRIIIP (ARG82P), ONE OF THE REGULATORS OF ARGININE METABOLISM IN SACCHAROMYCES-CEREVISIAE - ROLE IN EXPRESSION OF CELL-TYPE-SPECIFIC GENES

被引:44
作者
DUBOIS, E
MESSENGUY, F
机构
[1] CERIA,INST RECH,B-1070 BRUSSELS,BELGIUM
[2] FREE UNIV BRUSSELS,MICROBIOL LAB,BRUSSELS,BELGIUM
来源
MOLECULAR & GENERAL GENETICS | 1994年 / 243卷 / 03期
关键词
YEAST; ARGININE; CELL-TYPE REGULATION;
D O I
10.1007/BF00301067
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
ArgRIIIp (Arg82p), together with ArgRIp (Arg80p), ArgRIIp (Arg81p) and Mcm1p, regulates the expression of arginine anabolic and catabolic genes. An argRIII mutant constitutively expresses five anabolic enzymes and is impaired in the induction of the synthesis of two catabolic enzymes. A genomic disruption of the ARGRIII gene not only leads to an argR phenotype, but also prevents cell growth at 37 degrees C. The disrupted strain is sterile especially in an a background and transcription of alpha- and a-specific genes (MF alpha 1 and STE2) is strongly reduced. By gel retardation assays we show that the binding of the Mcm1p present in a crude protein extract from an argRIII mutant strain to the P(PAL) sequence is impaired. Sporulation of alpha/a argRIII::URA3 homozygous diploids is also affected. Overexpression of Mcm1p in an argRIII-disrupted strain restores the mating competence of the strain, the ability to form a protein complex with P(PAL) DNA in vitro, and the regulation of arginine metabolism. However, overexpression of Mcm1p does not complement the sporulation deficiency of the argRIII-disrupted strain, nor does it complement its growth defect at 37 degrees C. Western blot analysis indicates that Mcm1p is less abundant in a strain devoid of ArgRIIIp than in wild type.
引用
收藏
页码:315 / 324
页数:10
相关论文
共 49 条
[1]   METHOD FOR DETECTION OF SPECIFIC RNAS IN AGAROSE GELS BY TRANSFER TO DIAZOBENZYLOXYMETHYL-PAPER AND HYBRIDIZATION WITH DNA PROBES [J].
ALWINE, JC ;
KEMP, DJ ;
STARK, GR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1977, 74 (12) :5350-5354
[2]   IDENTIFICATION, PURIFICATION, AND CLONING OF A POLYPEPTIDE (PRTF/GRM) THAT BINDS TO MATING-SPECIFIC PROMOTER ELEMENTS IN YEAST [J].
AMMERER, G .
GENES & DEVELOPMENT, 1990, 4 (02) :299-312
[3]   MUTATIONS AFFECTING REPRESSIBILITY OF ARGININE BIOSYNTHETIC ENZYMES IN SACCHAROMYCES-CEREVISIAE [J].
BECHET, J ;
GRENSON, M ;
WIAME, JM .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1970, 12 (01) :31-+
[4]   MAT-ALPHA-1 PROTEIN, A YEAST TRANSCRIPTION ACTIVATOR, BINDS SYNERGISTICALLY WITH A 2ND PROTEIN TO A SET OF CELL-TYPE-SPECIFIC GENES [J].
BENDER, A ;
SPRAGUE, GF .
CELL, 1987, 50 (05) :681-691
[5]   REGULATION OF ARGININE METABOLISM IN SACCHAROMYCES-CEREVISIAE - EXPRESSION OF THE 3 ARGR REGULATORY GENES AND CELLULAR-LOCALIZATION OF THEIR PRODUCTS [J].
BERCY, J ;
DUBOIS, E ;
MESSENGUY, F .
GENE, 1987, 55 (2-3) :277-285
[6]   A FAMILY OF LOW AND HIGH COPY REPLICATIVE, INTEGRATIVE AND SINGLE-STRANDED SACCHAROMYCES-CEREVISIAE ESCHERICHIA-COLI SHUTTLE VECTORS [J].
BONNEAUD, N ;
OZIERKALOGEROPOULOS, O ;
LI, GY ;
LABOUESSE, M ;
MINVIELLESEBASTIA, L ;
LACROUTE, F .
YEAST, 1991, 7 (06) :609-615
[7]   FUNCTIONAL DOMAINS OF THE YEAST TRANSCRIPTION REPLICATION FACTOR MCM1 [J].
CHRIST, C ;
TYE, BK .
GENES & DEVELOPMENT, 1991, 5 (05) :751-763
[8]  
CHRIST C, 1992, THESIS CORNELL U
[9]   REGULATION OF ARGININE-BIOSYNTHESIS IN SACCHAROMYCES-CEREVISIAE - SPECIFICITY OF ARGR- MUTATIONS AND GENERAL CONTROL OF AMINO-ACID BIOSYNTHESIS [J].
DELFORGE, J ;
MESSENGUY, F ;
WIAME, JM .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1975, 57 (01) :231-239
[10]   CHARACTERIZATION OF 2 GENES, ARGRI AND ARGRIII REQUIRED FOR SPECIFIC REGULATION OF ARGININE METABOLISM IN YEAST [J].
DUBOIS, E ;
BERCY, J ;
MESSENGUY, F .
MOLECULAR & GENERAL GENETICS, 1987, 207 (01) :142-148