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Discrete models of biochemical networks Algebraic Biology 2007 RISC Linz, Austria July 3 , 2007. Reinhard Laubenbacher Virginia Bioinformatics Institute and Mathematics Department Virginia Tech. Polynomial dynamical systems. Let k be a finite field and f 1 , … , f n k [ x 1 ,…, x n ]
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Discrete models of biochemical networksAlgebraic Biology 2007RISC Linz, AustriaJuly 3, 2007 Reinhard Laubenbacher Virginia Bioinformatics Institute and Mathematics Department Virginia Tech
Polynomial dynamical systems Let k be a finite field and f1, … , fn k[x1,…,xn] f = (f1, … , fn) : kn → kn is an n-dimensional polynomial dynamical system over k. Natural generalization of Boolean networks. Fact: Every function kn → k can be represented by a polynomial, so all finite dynamical systems kn → kn are polynomial dynamical systems.
Example k = F3 = {0, 1, 2}, n = 3 f1 = x1x22+x3, f2 = x2+x3, f3 = x12+x22. Dependency graph (wiring diagram)
Motivation: Gene regulatory networks “[The] transcriptional control of a gene can be described by a discrete-valued function of several discrete-valued variables.” “A regulatory network, consisting of many interacting genes and transcription factors, can be described as a collection of interrelated discrete functions and depicted by a wiring diagram similar to the diagram of a digital logic circuit.” Karp, 2002
Network inference using finite dynamical systems models Variables x1, … , xn with values in k. (s1, t1), … , (sr, tr) state transition observations with sj, tjkn. Network inference: Identify a collection of “most likely” models/dynamical systems f=(f1, … ,fn): kn→ kn such that f(sj)=tj.
Important model information obtained from f=(f1, … ,fn): • The “wiring diagram” or “dependency graph” directed graph with the variables as vertices; there is an edge i → j if xi appears in fj. • The dynamics directed graph with the elements of kn as vertices; there is an edge u → v if f(u) = v.
The model space Let I be the ideal of the points s1, … , sr, that is, I = <f k[x1, … xn] | f(si)=0 for all i>. Let f = (f1, … , fn) be one particular feasible model. Then the space M of all feasible models is M = f + I = (f1 + I, … , fn + I).
Model selection Problem: The model space f + I is WAY TOO BIG Idea for Solution: Use “biological theory” to reduce it.
“Biological theory” • Limit the structure of the coordinate functions fi to those which are “biologically meaningful.” (Characterize special classes computationally.) • Limit the admissible dynamical properties of models. (Identify and computationally characterize classes for which dynamics can be predicted from structure.)
A non-canalyzing Boolean network f1 = x4 f2 = x4+x3 f3 = x2+x4 f4 = x2+x1+x3
A nested canalyzing Boolean network g1 = x4 g2 = x4*x3 g3 = x2*x4 g4 = x2*x1*x3
The algebraic geometry Corollary. The ideal of relations determining the class of nested canalyzing Boolean functions on n variables defines an affine toric variety Vncf over the algebraic closure of F2. The irreducible components correspond to the functions that are nested canalyzing with respect to a given variable ordering. That is, Vncf = Uσ Vσncf
Dynamics from structure Theorem. Let f = (f1, … , fn) : kn → kn be a monomial system. • If k = F2, then f is a fixed point system if and only if every strongly connected component of the dependency graph of f has loop number 1. (Colón-Reyes, L., Pareigis) • The case for general k can be reduced to the Boolean + linear case. (Colón-Reyes, Jarrah, L., Sturmfels)
Questions • What are good classes of functions from a biological and/or mathematical point of view? • What extra mathematical structure is needed to make progress? • How does the nature of the observed data points affect the structure of f + I and MX?
Open Problems Study stochastic polynomial dynamical systems. • Stochastic update order • Stochastic update functions
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