Predicting stochastic gene expression dynamics in single cells

被引:120
作者
Mettetal, Jerome T.
Muzzey, Dale
Pedraza, Juan M.
Ozbudak, Ertugrul M.
van Oudenaarden, Alexander
机构
[1] MIT, Dept Phys, Cambridge, MA 02139 USA
[2] Harvard Univ, Sch Med, Grad Biophys Program, Boston, MA 02115 USA
关键词
gene networks; systems biology;
D O I
10.1073/pnas.0509874103
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Fluctuations in protein numbers (noise) due to inherent stochastic effects in single cells can have large effects on the dynamic behavior of gene regulatory networks. Although deterministic models can predict the average network behavior, they fail to incorporate the stochasticity characteristic of gene expression, thereby limiting their relevance when single cell behaviors deviate from the population average. Recently, stochastic models have been used to predict distributions of steady-state protein levels within a population but not to predict the dynamic, presteadystate distributions. In the present work, we experimentally examine a system whose dynamics are heavily influenced by stochastic effects. We measure population distributions of protein numbers as a function of time in the Escherichia coli lactose uptake network (lac operon). We then introduce a dynamic stochastic model and show that prediction of dynamic distributions requires only a few noise parameters in addition to the rates that characterize a deterministic model. Whereas the deterministic model cannot fully capture the observed behavior, our stochastic model correctly predicts the experimental dynamics without any fit parameters. Our results provide a proof of principle for the possibility of faithfully predicting dynamic population distributions from deterministic models supplemented by a stochastic component that captures the major noise sources.
引用
收藏
页码:7304 / 7309
页数:6
相关论文
共 35 条
[1]   Enhancement of cellular memory by reducing stochastic transitions [J].
Acar, M ;
Becskei, A ;
van Oudenaarden, A .
NATURE, 2005, 435 (7039) :228-232
[2]  
Arkin A, 1998, GENETICS, V149, P1633
[3]   Bacterial persistence as a phenotypic switch [J].
Balaban, NQ ;
Merrin, J ;
Chait, R ;
Kowalik, L ;
Leibler, S .
SCIENCE, 2004, 305 (5690) :1622-1625
[4]   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
[5]   Noise in eukaryotic gene expression [J].
Blake, WJ ;
Kærn, M ;
Cantor, CR ;
Collins, JJ .
NATURE, 2003, 422 (6932) :633-637
[6]   On physiological multiplicity and population heterogeneity of biological systems [J].
Chung, JD ;
Stephanopoulos, G .
CHEMICAL ENGINEERING SCIENCE, 1996, 51 (09) :1509-1521
[7]   Regulated cell-to-cell variation in a cell-fate decision system [J].
Colman-Lerner, A ;
Gordon, A ;
Serra, E ;
Chin, T ;
Resnekov, O ;
Endy, D ;
Pesce, CG ;
Brent, R .
NATURE, 2005, 437 (7059) :699-706
[8]   Stochastic gene expression in a single cell [J].
Elowitz, MB ;
Levine, AJ ;
Siggia, ED ;
Swain, PS .
SCIENCE, 2002, 297 (5584) :1183-1186
[9]   EXACT STOCHASTIC SIMULATION OF COUPLED CHEMICAL-REACTIONS [J].
GILLESPIE, DT .
JOURNAL OF PHYSICAL CHEMISTRY, 1977, 81 (25) :2340-2361
[10]   Noise-based switches and amplifiers for gene expression [J].
Hasty, J ;
Pradines, J ;
Dolnik, M ;
Collins, JJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (05) :2075-2080