shenorr1

r1

∅ = Y

r2

Y = ∅

r3

∅ = Z

r4

Z = ∅

Global parameters
r1
r2
r3
r4

e3

Trigger: geq(time, 10)

Delay:

Assignments:

  • X = 1

e4

Trigger: geq(time, 15)

Delay:

Assignments:

  • X = 0

e2

Trigger: geq(time, 3.5)

Delay:

Assignments:

  • X = 0

e1

Trigger: geq(time, 3)

Delay:

Assignments:

  • X = 1

Note that constraints are not enforced in simulations. It remains the responsibility of the user to verify that simulation results satisfy these constraints.


Species:

Reactions:


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Network motifs in the transcriptional regulation network of Escherichia coli.

  • Shai S Shen-Orr
  • Ron Milo
  • Shmoolik Mangan
  • Uri Alon
Nat. Genet. 2002; 31 (1): 64-68
Abstract
Little is known about the design principles of transcriptional regulation networks that control gene expression in cells. Recent advances in data collection and analysis, however, are generating unprecedented amounts of information about gene regulation networks. To understand these complex wiring diagrams, we sought to break down such networks into basic building blocks. We generalize the notion of motifs, widely used for sequence analysis, to the level of networks. We define 'network motifs' as patterns of interconnections that recur in many different parts of a network at frequencies much higher than those found in randomized networks. We applied new algorithms for systematically detecting network motifs to one of the best-characterized regulation networks, that of direct transcriptional interactions in Escherichia coli. We find that much of the network is composed of repeated appearances of three highly significant motifs. Each network motif has a specific function in determining gene expression, such as generating temporal expression programs and governing the responses to fluctuating external signals. The motif structure also allows an easily interpretable view of the entire known transcriptional network of the organism. This approach may help define the basic computational elements of other biological networks.
The SBML for this model was obtained from the BioModels database (BioModels ID: BIOMD0000000316) Biomodels notes: Time course simulation as in figure 2A of the reference publication, showing that only persistent high levels of X leads to upregulation of Z. The simulation was performed using Copasi 4.6.33. JWS Online curation: This model was curated by reproducing the figures 2A. Only Y and Z were added.