Global role of TATA box-binding protein recruitment to promoters in mediating gene expression profiles

被引:52
作者
Kim, JW
Iyer, VR
机构
[1] Univ Texas, Inst Mol & Cellular Biol, Austin, TX 78712 USA
[2] Univ Texas, Sect Mol Genet & Microbiol, Austin, TX 78712 USA
关键词
D O I
10.1128/MCB.24.18.8104-8112.2004
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 recruitment of TATA box-binding protein (TBP) to promoters is one of the rate-limiting steps during transcription initiation. However, the global importance of TBP recruitment in determining the absolute and changing levels of transcription across the genome is not known. We used a genomic approach to explore the relationship between TBP recruitment to promoters and global gene expression profiles in Saccharomyces cerevisiae. Our data indicate that first, RNA polymerase III promoters are the most prominent binding targets of TBP in vivo. Second, the steady-state transcript levels of genes throughout the genome are proportional to the occupancy of their promoters by TBP, and changes in the expression levels of these genes are closely correlated with changes in TBP recruitment to their promoters. Third, a consensus TATA element does not appear to be a major determinant of either TBP binding or gene expression throughout the genome. Our results indicate that the recruitment of TBP to promoters in vivo is of universal importance in determining gene expression levels in yeast, regardless of the nature of the core promoter or the type of activator or repressor that may mediate changes in transcription. The primary data reported here are available at http://www.iyerlab.org/tbp.
引用
收藏
页码:8104 / 8112
页数:9
相关论文
共 42 条
[21]   Binding of TBP to promoters in vivo is stimulated by activators and requires Pol II holoenzyme [J].
Kuras, L ;
Struhl, K .
NATURE, 1999, 399 (6736) :609-613
[22]   Derepression of DNA damage-regulated genes requires yeast TAFIIs [J].
Li, B ;
Reese, JC .
EMBO JOURNAL, 2000, 19 (15) :4091-4100
[23]   Enhancement of TBP binding by activators and general transcription factors [J].
Li, XY ;
Virbasius, A ;
Zhu, XC ;
Green, MR .
NATURE, 1999, 399 (6736) :605-609
[24]   Promoter-specific binding of Rap1 revealed by genome-wide maps of protein-DNA association [J].
Lieb, JD ;
Liu, XL ;
Botstein, D ;
Brown, PO .
NATURE GENETICS, 2001, 28 (04) :327-334
[25]   TATA-BINDING PROTEIN-ASSOCIATED FACTOR(S) IN TFIID FUNCTION THROUGH THE INITIATOR TO DIRECT BASAL TRANSCRIPTION FROM A TATA-LESS CLASS-II PROMOTER [J].
MARTINEZ, E ;
CHIANG, CM ;
GE, H ;
ROEDER, RG .
EMBO JOURNAL, 1994, 13 (13) :3115-3126
[26]   Transfer RNA gene redundancy and translational selection in Saccharomyces cerevisiae [J].
Percudani, R ;
Pavesi, A ;
Ottonello, S .
JOURNAL OF MOLECULAR BIOLOGY, 1997, 268 (02) :322-330
[27]   Characterizing the physical genome [J].
Pollack, JR ;
Iyer, VR .
NATURE GENETICS, 2002, 32 (Suppl 4) :515-521
[28]   TRANSCRIPTION FROM A TATA-LESS PROMOTER REQUIRES A MULTISUBUNIT TFIID COMPLEX [J].
PUGH, BF ;
TJIAN, R .
GENES & DEVELOPMENT, 1991, 5 (11) :1935-1945
[29]   Control of gene expression through regulation of the TATA-binding protein [J].
Pugh, BF .
GENE, 2000, 255 (01) :1-14
[30]   The Skn7 response regulator of Saccharomyces cerevisiae interacts with Hsf1 in vivo and is required for the induction of heat shock genes by oxidative stress [J].
Raitt, DC ;
Johnson, AL ;
Erkine, AM ;
Makino, K ;
Morgan, B ;
Gross, DS ;
Johnston, LH .
MOLECULAR BIOLOGY OF THE CELL, 2000, 11 (07) :2335-2347