- About this Journal ·
- Abstracting and Indexing ·
- Aims and Scope ·
- Annual Issues ·
- Article Processing Charges ·
- Articles in Press ·
- Author Guidelines ·
- Bibliographic Information ·
- Citations to this Journal ·
- Contact Information ·
- Editorial Board ·
- Editorial Workflow ·
- Free eTOC Alerts ·
- Publication Ethics ·
- Reviewers Acknowledgment ·
- Submit a Manuscript ·
- Subscription Information ·
- Table of Contents

Journal of Applied Mathematics

Volume 2014 (2014), Article ID 730292, 11 pages

http://dx.doi.org/10.1155/2014/730292

## Finite-Time Stability Analysis of Switched Genetic Regulatory Networks

^{1}School of Control Science and Engineering, Shandong University, Jinan 250061, China^{2}School of Mathematical Sciences, University of Jinan, Jinan 250022, China

Received 11 October 2013; Revised 15 December 2013; Accepted 15 December 2013; Published 19 January 2014

Academic Editor: Qiankun Song

Copyright © 2014 Lizi Yin. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

#### Abstract

This paper investigates the finite-time stability problem of switching genetic regulatory networks (GRNs) with interval time-varying delays and unbounded continuous distributed delays. Based on the piecewise Lyapunov-Krasovskii functional and the average dwell time method, some new finite-time stability criteria are obtained in the form of linear matrix inequalities (LMIs), which are easy to be confirmed by the Matlab toolbox. The finite-time stability is taken into account in switching genetic regulatory networks for the first time and the average dwell time of the switching signal is obtained. Two numerical examples are presented to illustrate the effectiveness of our results.

#### 1. Introduction

In the last decade or so, the genetic regulatory networks (GRNs) have become an important research area in molecular Biology. On the one hand, how to construct GRNs from gene expression data; on the other hand, what is the dynamic characteristics of gene regulatory networks. The stability is one of vital dynamic characteristics of GRNs and is researched in this paper. There are also many references on the stability of GRNs [1–6].

High throughput biological experiments have proved that time delays were ubiquitous in GRNs. The existence of time delays influences the stability of GRNs, which can give rise to oscillatory or unstable networks. Therefore, it is necessary to study the influences of time delays for the stability of GRNs. There are a few theoretical results on GRNs with time delays [7–15]. In [2], random time delays are taken into account, and some stability criteria for the uncertain delayed genetic networks with SUM regulatory logic where each transcription factor acts additively to regulate a gene were obtained. In [12], some stochastic asymptotic stability conditions were established for a class of uncertain stochastic genetic regulatory networks with mixed time-varying delays by constructing appropriate Lyapunov-Krasovskii functionals and employing stochastic analysis method. In [13, 14], authors studied GRNs with constant delay, and asymptotical stability criteria were proposed for GRNs with interval time-varying delays and nonlinear disturbance in [10].

Cell-cycle regulatory processes can be viewed as finite-state processes. So some complex GRNs were described by continuous time switched system. Usually, a finite state Markov chain was used to simulate this switch process [16–19]. In [17], authors investigate the global robust stability of uncertain stochastic GRNs with Markovian switching process. In [19], control theory and mathematical tools were used to analyze passivity for the stochastic Markovian switching GRNs with time-varying delays. Some other methods are also used to prove switched GRNs’ stability. In the literature [20], authors used an average dwell time approach to consider exponential stability of switched GRNs with time delays.

Both procedures of these proteins regulate gene expression and gene translated protein that are sometimes accomplished in a relatively short period of time. So it is realistically significant to research the finite-time stability of GRNs and some articles have researched the finite-time stability [21, 22]. There are few references about the finite-time stability of GRNs; we research only the literature [23]. In [23], the authors considered finite-time robust stability of uncertain stochastic reaction-diffusion GRNs with time delays. The finite-time stability of GRNs is the main contents in our paper.

Motivated by the above discussions, we analyze finite-time stability of switching genetic regulatory networks with interval time-varying delays and continuous distributed delays. Using a novel piecewise Lyapunov-Krasovskii functional and finite-time stable definite, some new finite-time stability criteria are obtained for the switched GRNs. The features of this paper can be summarized as follows. the finite-time stability is researched in the switched GRNs firstly; continuous distributed delays are concerned; all sufficient conditions obtained depend on the time delays.

This paper is organized as follows. In Section 2, model description, some assumptions, definitions, and lemmas are given. In Section 3, some conditions are obtained to ensure the finite-time stability of switched GRNs with interval time-varying delays and continuous distributed delays. Two numerical examples are given to demonstrate the effectiveness of our analysis in Section 4. Finally, conclusions are drawn in Section 5.

*Notations*. Throughout this paper, , , and denote, respectively, the set of all real numbers, real -dimensional space, and real -dimensional space. denote the set of all positive integers. denote the Euclidean norms in . For a vector or matrix , denotes its transpose. For a square matrix , and denote the maximum eigenvalue and minimum eigenvalue of matrix , respectively, and sym () is used to represent . For simplicity, in symmetric block matrices, we often use to represent the term that is induced by symmetry.

#### 2. Problem Formulation and Some Preliminaries

We consider the following genetic regulatory networks: where is the concentrations of mRNAs, is the concentrations of proteins, is the regulatory functions of mRNAs, is the degradation rates of mRNAs, is the degradation rates of proteins, is the translation rates of proteins, is the basal rate, and and are time-varying delays.

For obtaining our conclusions, we make the following assumptions.

*Assumption 1. *, are monotonically increasing functions with saturation and satisfy
where , are nonnegative constants.

*Assumption 2. * and are time-varying delays satisfying

Vectors , are an equilibrium point of the system (1). Let , ; we get where , , , and .

According to Assumption 1 and the definition of , we know that is bounded; that is, , such that , and satisfies the following sector condition: Let .

Sometimes, GRNs were described by continuous time switched system, as in [17, 24, 25], so system (4) can be described as switching system with switching signal: where is the switching signal, which is a piecewise constant function depending on time . For each , the matrices , , , and are the th subsystem matrices that are constant matrices of appropriate dimensions.

For the switching signal , we have the following switching sequence: in other words, when , th subsystem is activated.

The initial condition of system (6) is assumed to be

For proving the theorem, we recall the following definition and lemmas.

*Definition 3. *The system (6) is said to be finite-time stable with respect to positive real numbers , if
where .

*Remark 4. *The Lyapunov stability implies that, by starting sufficiently close to the equilibrium point, trajectories can be guaranteed to stay within any specified ball centered at the equilibrium point. It depicts character of the equilibrium point of the system. The finite-time stability implies that, by starting from any specified compact set, trajectories can be guaranteed to stay within a large enough compact set. It depicts character of all solutions of the system and is called the finite-time boundedness in some literatures [21, 22]. In addition, the Lyapunov stability is considered in infinite interval, but the finite-time stability is considered in finite interval.

*Remark 5. *In [23], the authors considered the finite-time robust stability of GRNs, but in our paper we considered the finite-time stability of switching GRNs, which are more realistic GRNs than that of the [23]. For the first time switched GRNs’ finite-time stability is researched.

*Definition 6. *For any , let denote the number of switching of over . If
holds for , , then is called the average dwell time and is the chatter bound. As commonly used in the literature, we choose .

Lemma 7 (see [26]). *For any positive definite matrix , there exist a scalar and a vector-valued function such that
*

*3. Main Results*

*In this section, we present a finite time stability theorem for switching genetic regulatory networks with interval time-varying delays (6).*

*Theorem 8. For switching system (6) with Assumptions 1 and 2, given a scalar , if there exist symmetric positive definite matrices , , , , , , , for all , the diagonal matrix , , matrices , , , , and positive scalars such that the following inequalities
hold, and the average dwell time of the switching signal satisfies
where , , ,, , , , , , . The equilibrium point of (6) is finite time stable with respect to positive real numbers .*

*Proof. *Based on the system (6), we construct the following Lyapunov-krasovskii functional:
where
First, when , taking the derivatives of , along the trajectory of system (6), we have that
By Lemma 7, we have

Similar to (20), we can obtain
In addition, for any , , the following inequality is true from (5):
It can be written as matrix form:
From (15) to (23), we have that
where
By condition (13), we have
Integrating (26) from to , we obtain that
Using (12), at switching instant , we have
Therefore, it follows from (27) and (28) that
For any , noting that , we have
On the other hand, it follows from (15) that
From (30) and (31) it is easy to obtain
where
By (14) and (32), for any , we obtain that
This completes the proof.

*Next, we consider the finite-time stability of the genetic regulatory networks with time-varying delays and unbounded continuous distributed delays:
where is the switching signal, the matrix , , is the th subsystem distributively delayed connection weight matrix of appropriate dimension, is the delay kernel function, and all the other signs are defined as (6).*

*Assumption 9. *The delay kernel ’s are some real value nonnegative continuous functions defined in , that satisfy

*Theorem 10. For switching system (35) with Assumptions 1–9, given a scalar , if there exist symmetric positive definite matrices , , , , , , , the positive definite diagonal matrix , for all , , , matrices , , , , and positive scalars such that the following inequalities
hold, and the average dwell time of the switch signal satisfies
where , , , , , , , , , , , , , . The equilibrium point of (35) is finite time stable with respect to positive real numbers .*

*Proof. *Based on the system (35), we construct the following Lyapunov-krasovskii functional:
where , , are defined as in Theorem 8,
when ; taking the derivatives of along the trajectory of system (35), we have that
By Cauchy’s inequality , we obtain that
Therefore,
Combing (17)–(23) and (40)–(43), we get
where
Similar to the proof of Theorem 8, for any , we have that
where
By (39) and (47), we obtain that
This completes the proof.

*4. Numerical Examples*

*In this section, we will give two examples to show the effectiveness of our results. The aim is to examine the finite-time stability for gene networks under proper conditions by applying Theorems 8 and 10.*

*Example 1. *Consider a genetic regulatory network model reported by Elowitz and Leibler [27], which studied the dynamics of repressilator which is cyclic negative-feedback loop comprising three repressor genes (*acl*, *tetR*, *and cl*) and their promoters (*l*, *lacl*, *and tetR*):
where and are the concentrations of two mRNAs and repressor-protein; is the growth rate of protein in a cell in the presence of saturating amounts of repressor, while is the growth rate in its abscence; denotes the ratio of the protein decay rate to mRNA decay rate; and is a Hill coefficient.

Taking time-varying delays and mode switching into account, we rewrite the above equation into vector form by adjusting some parameters and shifting the equilibrium point to the origin, and then we get the following model:
where

The gene regulation function is taken as , . The time delays and are assumed to be:
we can get the parameters as following:
and let , , , , . By using the Matlab LMI toolbox, we can solve the LMIs (12), (13) and obtain feasible solutions. Equation (13) can be reformulated in the following in the form of LMI:where , , , , , , , , .

Due to the space limitation, we only list matrices , , , and here:
and . The initial condition is , . The simulation results of the trajectories are shown in Figures 1 and 2.

*Example 2. *In this example, we consider the genetic regulatory (35) with time-varying delays and unbounded continuous distributed delays, in which the parameters are listed as follows:
and , . The time delays and are assumed to be
we can get the parameters as following:
and let , , ,