Activity motifs reveal principles of timing in transcriptional control of the yeast metabolic network

被引:127
作者
Chechik, Gal [3 ]
Oh, Eugene [4 ,5 ]
Rando, Oliver [6 ]
Weissman, Jonathan [4 ,5 ]
Regev, Aviv [1 ,2 ]
Koller, Daphne [3 ]
机构
[1] MIT, Dept Biol, Cambridge, MA 02142 USA
[2] Broad Inst MIT & Harvard, Cambridge, MA 02142 USA
[3] Stanford Univ, Dept Comp Sci, Stanford, CA 94305 USA
[4] Univ Calif San Francisco, Howard Hughes Med Fdn, San Francisco, CA 94143 USA
[5] Univ Calif San Francisco, Dept Cellular & Mol Pharmacol, San Francisco, CA 94143 USA
[6] Univ Massachusetts, Sch Med, Dept Mol Pharmacol & Biochem, Worcester, MA 01655 USA
基金
美国国家科学基金会;
关键词
D O I
10.1038/nbt.1499
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Significant insight about biological networks arises from the study of network motifs-overly abundant network subgraphs(1,2)-but such wiring patterns do not specify when and how potential routes within a cellular network are used. To address this limitation, we introduce activity motifs, which capture patterns in the dynamic use of a network. Using this framework to analyze transcription in Saccharomyces cerevisiae metabolism, we find that cells use different timing activity motifs to optimize transcription timing in response to changing conditions: forward activation to produce metabolic compounds efficiently, backward shutoff to rapidly stop production of a detrimental product and synchronized activation for co-production of metabolites required for the same reaction. Measuring protein abundance over a time course reveals that mRNA timing motifs also occur at the protein level. Timing motifs significantly overlap with binding activity motifs, where genes in a linear chain have ordered binding affinity to a transcription factor, suggesting a mechanism for ordered transcription. Finely timed transcriptional regulation is therefore abundant in yeast metabolism, optimizing the organism's adaptation to new environmental conditions.
引用
收藏
页码:1251 / 1259
页数:9
相关论文
共 47 条
[1]   Noise in protein expression scales with natural protein abundance [J].
Bar-Even, Arren ;
Paulsson, Johan ;
Maheshri, Narendra ;
Carmi, Miri ;
O'Shea, Erin ;
Pilpel, Yitzhak ;
Barkai, Naama .
NATURE GENETICS, 2006, 38 (06) :636-643
[2]   Analyzing time series gene expression data [J].
Bar-Joseph, Z .
BIOINFORMATICS, 2004, 20 (16) :2493-2503
[3]   Quantification of protein half-lives in the budding yeast proteome [J].
Belle, Archana ;
Tanay, Amos ;
Bitincka, Ledion ;
Shamir, Ron ;
O'Shea, Erin K. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (35) :13004-13009
[4]   Conservation of expression and sequence of metabolic genes is reflected by activity across metabolic states [J].
Bilu, Yonatan ;
Shlomi, Tomer ;
Barkai, Naama ;
Ruppin, Eytan .
PLOS COMPUTATIONAL BIOLOGY, 2006, 2 (08) :932-938
[5]   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
[6]  
CHECHIK G, J CELL BIOL IN PRESS
[7]   Dynamics and design principles of a basic regulatory architecture controlling metabolic pathways [J].
Chin, Chen-Shan ;
Chubukov, Victor ;
Jolly, Emmitt R. ;
DeRisi, Joe ;
Li, Hao .
PLOS BIOLOGY, 2008, 6 (06) :1343-1356
[8]   The fluxes through glycolytic enzymes in Saccharomyces cerevisiae are predominantly regulated at posttranscriptional levels [J].
Daran-Lapujade, Pascale ;
Rossell, Sergio ;
van Gulik, Walter M. ;
Luttik, Marijke A. H. ;
de Groot, Marco J. L. ;
Slijper, Monique ;
Heck, Albert J. R. ;
Daran, Jean-Marc ;
de Winde, Johannes H. ;
Westerhoff, Hans V. ;
Pronk, Jack T. ;
Bakker, Barbara M. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2007, 104 (40) :15753-15758
[9]   Exploring the metabolic and genetic control of gene expression on a genomic scale [J].
DeRisi, JL ;
Iyer, VR ;
Brown, PO .
SCIENCE, 1997, 278 (5338) :680-686
[10]   Genome-scale reconstruction of the Saccharomyces cerevisiae metabolic network [J].
Förster, J ;
Famili, I ;
Fu, P ;
Palsson, BO ;
Nielsen, J .
GENOME RESEARCH, 2003, 13 (02) :244-253