Frequency domain analysis of noise in simple gene circuits

被引:36
作者
Cox, Chris D. [1 ]
McCollum, James M.
Austin, Derek W.
Allen, Michael S.
Dar, Roy D.
Simpson, Michael L.
机构
[1] Univ Tennessee, Dept Civil & Environm Engn, Knoxville, TN 37996 USA
[2] Univ Tennessee, Ctr Environm Biotechnol, Knoxville, TN 37996 USA
[3] Univ Tennessee, Dept Elect & Comp Engn, Knoxville, TN 37996 USA
[4] Siemens Mol Imaging, Knoxville, TN 37932 USA
[5] Oak Ridge Natl Lab, Mol Scale Engn & Nanoscale Technol Res Grp, Oak Ridge, TN 37831 USA
[6] Univ Tennessee, Dept Mat Sci, Knoxville, TN 37996 USA
[7] Univ Tennessee, Dept Phys, Knoxville, TN 37996 USA
基金
美国国家科学基金会;
关键词
D O I
10.1063/1.2204354
中图分类号
O29 [应用数学];
学科分类号
070104 ;
摘要
Recent advances in single cell methods have spurred progress in quantifying and analyzing stochastic fluctuations, or noise, in genetic networks. Many of these studies have focused on identifying the sources of noise and quantifying its magnitude, and at the same time, paying less attention to the frequency content of the noise. We have developed a frequency domain approach to extract the information contained in the frequency content of the noise. In this article we review our work in this area and extend it to explicitly consider sources of extrinsic and intrinsic noise. First we review applications of the frequency domain approach to several simple circuits, including a constitutively expressed gene, a gene regulated by transitions in its operator state, and a negatively autoregulated gene. We then review our recent experimental study, in which time-lapse microscopy was used to measure noise in the expression of green fluorescent protein in individual cells. The results demonstrate how changes in rate constants within the gene circuit are reflected in the spectral content of the noise in a manner consistent with the predictions derived through frequency domain analysis. The experimental results confirm our earlier theoretical prediction that negative autoregulation not only reduces the magnitude of the noise but shifts its content out to higher frequency. Finally, we develop a frequency domain model of gene expression that explicitly accounts for extrinsic noise at the transcriptional and translational levels. We apply the model to interpret a shift in the autocorrelation function of green fluorescent protein induced by perturbations of the translational process as a shift in the frequency spectrum of extrinsic noise and a decrease in its weighting relative to intrinsic noise.
引用
收藏
页数:15
相关论文
共 51 条
[1]  
Andersen JB, 1998, APPL ENVIRON MICROB, V64, P2240
[2]  
[Anonymous], 1940, The Journal of Chemical Physics, DOI [DOI 10.1063/1.1750549, 10.1063/1.1750549]
[3]  
Arkin A, 1998, GENETICS, V149, P1633
[4]   Gene network shaping of inherent noise spectra [J].
Austin, DW ;
Allen, MS ;
McCollum, JM ;
Dar, RD ;
Wilgus, JR ;
Sayler, GS ;
Samatova, NF ;
Cox, CD ;
Simpson, ML .
NATURE, 2006, 439 (7076) :608-611
[5]   Quantitative models of nuclear transport [J].
Becskei, A ;
Mattaj, LW .
CURRENT OPINION IN CELL BIOLOGY, 2005, 17 (01) :27-34
[6]  
Bendat J.S., 2000, RANDOM DATA ANAL MEA
[7]   Noise in eukaryotic gene expression [J].
Blake, WJ ;
Kærn, M ;
Cantor, CR ;
Collins, JJ .
NATURE, 2003, 422 (6932) :633-637
[8]   Efficient formulation of the stochastic simulation algorithm for chemically reacting systems [J].
Cao, Y ;
Li, H ;
Petzold, L .
JOURNAL OF CHEMICAL PHYSICS, 2004, 121 (09) :4059-4067
[9]   Tetracycline antibiotics: Mode of action, applications, molecular biology, and epidemiology of bacterial resistance [J].
Chopra, I ;
Roberts, M .
MICROBIOLOGY AND MOLECULAR BIOLOGY REVIEWS, 2001, 65 (02) :232-+
[10]   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