The TATA-binding protein is not an essential target of the transcriptional activators Gal4p and Gcn4p in Saccharomyces cerevisiae

被引:5
作者
Bongards, C [1 ]
Chew, BS [1 ]
Lehming, N [1 ]
机构
[1] Natl Univ Singapore, Fac Med, Dept Microbiol, Singapore 117597, Singapore
关键词
activation; mutation; protein-protein interaction; split-ubiquitin; transcription;
D O I
10.1042/BJ20021548
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
According to the recruitment model, transcriptional activators work by increasing the local concentration of one or several limiting factors for the transcription process at the target promoter. The TATA-binding protein Tbp1 has been considered as a likely candidate for such a limiting factor. We have used a series of Gal4p and Tbp1 mutants to correlate the in vivo interaction between the two proteins with the strength of activation. We find a clear correlation between activation strength and in vivo interaction for the series of Gal4p mutants. Consistently, the weaker activator Gcn4p does not interact with Tbp1. However, a corresponding analysis of the series of Tbp1 mutants revealed that Tbp1 is not an essential target of the acidic activators Gal4p and Gcn4p. Furthermore, detailed analysis of a Tbp1 mutant deficient for transcriptional activation by Gal4p revealed that the mutant is defective in interactions with five other proteins involved in the process of transcription.
引用
收藏
页码:141 / 147
页数:7
相关论文
共 43 条
[1]  
Ausubel FM., 1998, CURRENT PROTOCOLS MO
[2]   SAGA is an essential in vivo target of the yeast acidic activator Gal4p [J].
Bhaumik, SR ;
Green, MR .
GENES & DEVELOPMENT, 2001, 15 (15) :1935-1945
[3]   AN ESSENTIAL YEAST GENE ENCODING A HOMOLOG OF UBIQUITIN-ACTIVATING ENZYME [J].
DOHMEN, RJ ;
STAPPEN, R ;
MCGRATH, JP ;
FORROVA, H ;
KOLAROV, J ;
GOFFEAU, A ;
VARSHAVSKY, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (30) :18099-18109
[4]   Detection of transient in vivo interactions between substrate and transporter during protein translocation into the endoplasmic reticulum [J].
Dünnwald, M ;
Varshavsky, A ;
Johnsson, N .
MOLECULAR BIOLOGY OF THE CELL, 1999, 10 (02) :329-344
[5]   A NOVEL GENETIC SYSTEM TO DETECT PROTEIN PROTEIN INTERACTIONS [J].
FIELDS, S ;
SONG, OK .
NATURE, 1989, 340 (6230) :245-246
[6]   Crystal structure of the yeast TFIIA/TBP/DNA complex [J].
Geiger, JH ;
Hahn, S ;
Lee, S ;
Sigler, PB .
SCIENCE, 1996, 272 (5263) :830-836
[7]   NEW YEAST-ESCHERICHIA-COLI SHUTTLE VECTORS CONSTRUCTED WITH INVITRO MUTAGENIZED YEAST GENES LACKING 6-BASE PAIR RESTRICTION SITES [J].
GIETZ, RD ;
SUGINO, A .
GENE, 1988, 74 (02) :527-534
[8]   A subset of TAFIIs are integral components of the SAGA complex required for nucleosome acetylation and transcriptional stimulation [J].
Grant, PA ;
Schieltz, D ;
Pray-Grant, MG ;
Steger, DJ ;
Reese, JC ;
Yates, JR ;
Workman, JL .
CELL, 1998, 94 (01) :45-53
[9]   Srb7p is a physical and physiological target of Tup1p [J].
Gromöller, A ;
Lehming, N .
EMBO JOURNAL, 2000, 19 (24) :6845-6852
[10]   Evidence that Ga111 protein is a target of the Ga14 activation domain in the mediator [J].
Jeong, CJ ;
Yang, SH ;
Xie, YQ ;
Zhang, L ;
Johnston, SA ;
Kodadek, T .
BIOCHEMISTRY, 2001, 40 (31) :9421-9427