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. 2012 May 2;102(9):2186–2191. doi: 10.1016/j.bpj.2012.03.060

Figure 2.

Figure 2

Fluctuations in mRNA level in the case of diffusion in a dilute environment, leading to noncompact exploration. The nucleus volume is V=103μm3, and we take D=1μm2/s, and m=5. (A) Typical evolution of the mRNA copy number, nM(t) (red line), obtained by numerical simulations of the model for n = 10, λd=0.02min1. Here, the nucleus is modeled as a 3-dimensional cubic lattice and T=648min. Green bars mark the activation of the gene. (B) Waiting-time distribution, fn(T), between activation events for n = 1 (violet circles) and n = 10 (magenta triangles), compared to the theoretical prediction, derived in the Supporting Material (plain and dashed lines, respectively). (C) Normalized autocorrelation function RM(t)/n for diffusion on a 3-dimensional cubic lattice. Numerical simulations (symbols) for different values of λd and n are compared to the theoretical prediction (plain and dashed lines). λd=0.1min1 (n = 1 (green circles) and n = 10 (light green crosses)); λd=0.02min1 (n = 1 (dark blue triangles) and n = 10 (light blue inverted triangles)); λd=0.005min1 (n = 1 (red triangles) and n = 10 (orange triangles)). The dotted line is obtained by assuming a homogeneous concentration c0=1/V of TFs in infinite space (case λd=0.02min1). (D) Normalized autocorrelation function RM(t)/n for diffusion with dilute obstacles (here modeled by a 3-dimensional supercritical percolation cluster with p=0.8). λd=0.02min1 (n = 1 (dark blue triangles) and n = 10 (light blue inverted triangles)); λd=0.005min1 (n = 1 (red triangles) and n = 10 (orange triangles)).