Control and signal processing by transcriptional interference

被引:22
作者
Buetti-Dinh, Antoine [1 ]
Ungricht, Rosemarie [1 ]
Kelemen, Janos Z. [1 ]
Shetty, Chetak [1 ]
Ratna, Prasuna [1 ]
Becskei, Attila [1 ]
机构
[1] Univ Zurich, Inst Mol Biol, CH-8057 Zurich, Switzerland
关键词
noncoding transcription; promoter; repression; GENE-EXPRESSION; INTERGENIC TRANSCRIPTION; SACCHAROMYCES-CEREVISIAE; NONCODING TRANSCRIPTION; BIDIRECTIONAL PROMOTERS; ESCHERICHIA-COLI; FEEDFORWARD LOOP; RNA-POLYMERASE; YEAST; REPRESSOR;
D O I
10.1038/msb.2009.61
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
A transcriptional activator can suppress gene expression by interfering with transcription initiated by another activator. Transcriptional interference has been increasingly recognized as a regulatory mechanism of gene expression. The signals received by the two antagonistically acting activators are combined by the polymerase trafficking along the DNA. We have designed a dual-control genetic system in yeast to explore this antagonism systematically. Antagonism by an upstream activator bears the hallmarks of competitive inhibition, whereas a downstream activator inhibits gene expression non-competitively. When gene expression is induced weakly, the antagonistic activator can have a positive effect and can even trigger paradoxical activation. Equilibrium and non-equilibrium models of transcription shed light on the mechanism by which interference converts signals, and reveals that self-antagonism of activators imitates the behavior of feed-forward loops. Indeed, a synthetic circuit generates a bell-shaped response, so that the induction of expression is limited to a narrow range of the input signal. The identification of conserved regulatory principles of interference will help to predict the transcriptional response of genes in their genomic context. Molecular Systems Biology 5: 300; published online 18 August 2009; doi: 10.1038/msb.2009.61
引用
收藏
页数:8
相关论文
共 39 条
[1]   Noncoding transcription controls downstream promoters to regulate T-cell receptor α recombination [J].
Abarrategui, Iratxe ;
Krangel, Michael S. .
EMBO JOURNAL, 2007, 26 (20) :4380-4390
[2]   A synthetic multicellular system for programmed pattern formation [J].
Basu, S ;
Gerchman, Y ;
Collins, CH ;
Arnold, FH ;
Weiss, R .
NATURE, 2005, 434 (7037) :1130-1134
[3]   Contributions of low molecule number and chromosomal positioning to stochastic gene expression [J].
Becskei, A ;
Kaufmann, BB ;
van Oudenaarden, A .
NATURE GENETICS, 2005, 37 (09) :937-944
[4]   Role of the transcription activator Ste12p as a repressor of PRY3 expression [J].
Bickel, Kellie S. ;
Morris, David R. .
MOLECULAR AND CELLULAR BIOLOGY, 2006, 26 (21) :7901-7912
[5]   The Zap1 transcriptional activator also acts as a repressor by binding downstream of the TATA box in ZRT2 [J].
Bird, AJ ;
Blankman, E ;
Stillman, DJ ;
Eide, DJ ;
Winge, DR .
EMBO JOURNAL, 2004, 23 (05) :1123-1132
[6]   Repression of ADH1 and ADH3 during zinc deficiency by Zap1-induced intergenic RNA transcripts [J].
Bird, Amanda J. ;
Gordon, Mat ;
Eide, David J. ;
Winge, Dennis R. .
EMBO JOURNAL, 2006, 25 (24) :5726-5734
[7]   A BACTERIAL REPRESSOR PROTEIN OR A YEAST TRANSCRIPTIONAL TERMINATOR CAN BLOCK UPSTREAM ACTIVATION OF A YEAST GENE [J].
BRENT, R ;
PTASHNE, M .
NATURE, 1984, 312 (5995) :612-615
[8]   On schemes of combinatorial transcription logic [J].
Buchler, NE ;
Gerland, U ;
Hwa, T .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (09) :5136-5141
[9]   Reorganization of adjacent gene relationships in yeast genomes by whole-genome duplication and gene deletion [J].
Byrnes, Jake K. ;
Morris, Geoffrey P. ;
Li, Wen-Hsiung .
MOLECULAR BIOLOGY AND EVOLUTION, 2006, 23 (06) :1136-1143
[10]   Gene length and proximity to neighbors affect genome-wide expression levels [J].
Chiaromonte, F ;
Miller, W ;
Bouhassira, EE .
GENOME RESEARCH, 2003, 13 (12) :2602-2608