Combined global localization analysis and transcriptome data identify genes that are directly coregulated by Adr1 and Cat8

被引:129
作者
Tachibana, C
Yoo, JY
Tagne, JB
Kacherovsky, N
Lee, TI
Young, ET
机构
[1] Univ Washington, Dept Biochem, Seattle, WA 98195 USA
[2] Whitehead Inst Biomed Res, Cambridge, MA 02142 USA
关键词
D O I
10.1128/MCB.25.6.2138-2146.2005
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
In Saccharomyces cerevisiae, glucose depletion causes a profound alteration in metabolism, mediated in part by global transcriptional changes. Many of the transcription factors that regulate these changes act combinatorially. We have analyzed combinatorial regulation by Adr1 and Cat8, two transcription factors that act during glucose depletion, by combining genome-wide expression and genome-wide binding data. We identified 32 genes that are directly activated by Adr1, 28 genes that are directly activated by Cat8, and 14 genes that are directly regulated by both. Our analysis also uncovered promoters that Adr1 binds but does not regulate and promoters that are indirectly regulated by Cat8, stressing the advantage of combining global expression and global localization analysis to find directly regulated targets. At most of the coregulated promoters, the in vivo binding of one factor is independent of the other, but Adr1 is required for optimal Cat8 binding at two promoters with a poor match to the Cat8 binding consensus. In addition, Cat8 is required for Adr1 binding at promoters where Adr1 is not required for transcription. These data provide a comprehensive analysis of the direct, indirect, and combinatorial requirements for these two global transcription factors.
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收藏
页码:2138 / 2146
页数:9
相关论文
共 53 条
[1]   Quantifying the relationship between co-expression, co-regulation and gene function [J].
Allocco, DJ ;
Kohane, IS ;
Butte, AJ .
BMC BIOINFORMATICS, 2004, 5 (1)
[2]   Cooperative binding interactions required for function of the Ty1 sterile responsive element [J].
Baur, M ;
Esch, RK ;
Errede, B .
MOLECULAR AND CELLULAR BIOLOGY, 1997, 17 (08) :4330-4337
[3]   REGULATION OF EXPRESSION AND ACTIVITY OF THE YEAST TRANSCRIPTION FACTOR ADR1 [J].
BLUMBERG, H ;
HARTSHORNE, TA ;
YOUNG, ET .
MOLECULAR AND CELLULAR BIOLOGY, 1988, 8 (05) :1868-1876
[4]   The succinate/fumarate transporter Acr1p of Saccharomyces cerevisiae is part of the gluconeogenic pathway and its expression is regulated by Cat8p [J].
Bojunga, N ;
Kötter, P ;
Entian, KD .
MOLECULAR AND GENERAL GENETICS, 1998, 260 (05) :453-461
[5]   Cat8p, the activator of gluconeogenic genes in Saccharomyces cerevisiae, regulates carbon source-dependent expression of NADP-dependent cytosolic isocitrate dehydrogenase (Idp2p) and lactate permease (Jen1p) [J].
Bojunga, N ;
Entian, KD .
MOLECULAR AND GENERAL GENETICS, 1999, 262 (4-5) :869-875
[6]   Dissection of the promoter of the HAP4 gene in S-cerevisiae unveils a complex regulatory framework of transcriptional regulation [J].
Brons, JF ;
de Jong, M ;
Valens, M ;
Grivell, LA ;
Bolotin-Fukuhara, M ;
Blom, J .
YEAST, 2002, 19 (11) :923-932
[7]   A MECHANISM FOR SYNERGISTIC ACTIVATION OF A MAMMALIAN GENE BY GAL4 DERIVATIVES [J].
CAREY, M ;
LIN, YS ;
GREEN, MR ;
PTASHNE, M .
NATURE, 1990, 345 (6273) :361-364
[8]   Glucose repression in yeast [J].
Carlson, M .
CURRENT OPINION IN MICROBIOLOGY, 1999, 2 (02) :202-207
[9]   Constitutive and carbon source-responsive promoter elements are involved in the regulated expression of the Saccharomyces cerevisiae malate synthase gene MLS1 [J].
Caspary, F ;
Hartig, A ;
Schuller, HJ .
MOLECULAR & GENERAL GENETICS, 1997, 255 (06) :619-627
[10]   Remodeling of yeast genome expression in response to environmental changes [J].
Causton, HC ;
Ren, B ;
Koh, SS ;
Harbison, CT ;
Kanin, E ;
Jennings, EG ;
Lee, TI ;
True, HL ;
Lander, ES ;
Young, RA .
MOLECULAR BIOLOGY OF THE CELL, 2001, 12 (02) :323-337