Mathematical Problems in Engineering
Volume 2015 (2015), Article ID 303918, 5 pages
http://dx.doi.org/10.1155/2015/303918

Research Article

Analysis on Global Asymptotical Stability of Genetic Regulatory Networks with Time-Varying Delays via Convex Combination Method

Yang Liu¹ and Haixia Wu2,3

¹Department of Computer Engineering, Sichuan Vocational and Technical College of Communications, Chengdu 611130, China
²College of Automation, Chongqing University, Chongqing 400044, China
³Department of Mathematics and Information Engineering, Chongqing University of Education, Chongqing 400065, China

Received 7 June 2014; Accepted 22 July 2014

Academic Editor: Chuandong Li

Copyright © 2015 Yang Liu and Haixia Wu. 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.

The global asymptotical stability analysis for genetic regulatory networks with time delays is concerned. By using Lyapunov functional theorem, LMIs, and convex combination method, a new delay-dependent stability criterion has been presented in terms of LMIs to guarantee the delayed genetic regulatory networks to be asymptotically stable. The restriction that the derivatives of the time-varying delays are less than one is removed. Our result is applicable to both fast and slow time-varying delays. The stability criterion has less conservative and wider application range. Experimental result has been used to demonstrate the usefulness of the main results and less conservativeness of the proposed method.

1. Introduction

Genetic regulatory networks (GRNs) play a key role in systems biology as they explain the interactions between genes (mRNA) and proteins. In a biological cell, genes may be expressed constantly (i.e., constitutive gene expression) or expressed based on molecular signals (i.e., regulated gene expression) [1–3]. The central dogma of molecular biology states that gene expression consists of two main processes, namely, transcription and translation for prokaryotes, and with the additional step of ribonucleic acid (RNA) splicing for eukaryotes. In the transcriptional process, messenger RNAs (mRNAs) are synthesized from genes by the regulations of transcript factors, which are proteins. In the translational process, the sequence of nucleotides in the mRNA is used in the synthesis of a protein. A genetic regulatory network (GRN) is a nonlinear dynamical system which describes the highly complex interactions between mRNAs and proteins—two main genetic products produced in the transcriptional and translational processes. Nowadays, in systems biology, one of the main challenges is to understand the genetic regulatory networks, for example, how biological activities are governed by the connectivity of genes and proteins. The study of the nature and functions of GRN has already aroused the interest of many researchers.

Since 1960s, many notable researchers have proposed various kinds of mathematical models to describe GRN. So far, during the past few years, there are two basic models for genetic network models: the Boolean model and the differential equation model [2, 3]. In Boolean models, the expression of each gene in the network is assumed to be either ON or OFF, no “intermediate” activity levels are ever taken into consideration, and the state of a gene is determined by a Boolean function of the states of other related genes. The differential equation model describes the rates of change of the concentrations of gene products, such as mRNAs and proteins, as continuous values. The differential equation model is often preferred over the Boolean model because its accuracy is more secured. In practical biological model, gene expression rates are usually continuous variables rather than ideal ON-OFF switches. Several typical genetic regulatory networks have been modelled and studied experimentally and/or theoretically; see [4–6] for some recent results.

On the other hand, time delays which usually exist in transcription, translation, diffusion, and translocation processes especially in a eukaryotic cell are one of the key factors affecting the dynamics of genetic regulatory network. The delays could be time invariant or time variant. The study of stability is essential for designing or controlling genetic regulatory networks. Up to now, there are already some sufficient conditions that have been proposed to guarantee the asymptotic or robust stability for genetic regulatory networks [7–20].

Motivated by the above discussions, we aim to analyze the stability of genetic regulatory networks with SUM logic in the forms of differential equations. Besides the basic case, we will make contributions on the issues of asymptotical stability for genetic networks with time-varying delays. By choosing an appropriate new Lyapunov functional and employing convex combination method, new delay-derivative-dependent stability criterion is derived based on the consideration of ranges for the time-varying delays. The obtained criterion is given in terms of linear matrix inequalities (LMIs) and is applicable to both fast and slow time-varying delays. Finally, one numerical example is given to demonstrate the effectiveness and the merit of the proposed method.

2. Problem Description and Preliminaries

In [8, 9], the following differential equations have been used to describe GRNs containing mRNAs and proteins:

where , , and are the concentrations of mRNA and protein of the th node at time , respectively; and denote the degradation or dilution rates of mRNAs and proteins; and are the coupling matrices, and is defined as follows:

Furthermore, nonlinear function represents the feedback regulation of the protein on the transcription, which is the monotonic function in Hill form, , is the Hill coefficient, and and are the time-varying delays satisfying , , respectively; , where and is the set of all nodes which are repressors of gene .

In the following, we will always shift an intended equilibrium point of the system (1) to the origin by letting , . Hence, system (1) can be transformed into the following form:

where . Since is a monotonically increasing function with saturation, it satisfies, for all, with and . From the relationship of and , we know that satisfies the sector condition

Lemma 1 (Schur complement). Given constant symmetric matrices , , and , where and , then if and only if

3. Main Result

Theorem 2. For given scalars , , , and , system (1) is asymptotically stable, if there exist matrices , , , , , , , , , , , , such that the following LMIs (6) hold:

with

Proof. The Lyapunov functional of system (1) is defined by

Calculating the derivative of along the solutions of system (1), one can get

From the Leibniz-Newton formula, the following equations are true for any matrices , with appropriate dimensions:

with ,

In addition, from (4), we have , and , . Thus, for any , , it follows that

Combining (9)–(18), it follows that

where and

Thus, when , we have

It follows from Lyapunov-Krasovskii stability theorem that system (1) with time-varying delays is asymptotically stable.
Notice that is a convex combination of matrices and on satisfying , and is a convex combination of matrices and on satisfying . Then only if

Applying Lemma 1 (Schur complement) to the four inequalities above, we arrive at LMI (6).

Remark 3. In [7, 13], additional information regarding the derivatives of the time-varying delays is needed; that is , . From Theorem 2, one can see that the restrictions are removed. In this case, the results in [13] may produce conservative results. Our result is applicable to both fast and slow time-varying delays.

4. Numerical Example

Example 1. Consider the following genetic regulatory networks with time-varying delays, borrowed from [8, 9]:

in which

Using LMI Control Toolbox, by our Theorem 2, we can find that system (1) described by Example 1 is asymptotically stable. Limited to the length of the paper, we only show a part of the feasible solution here:

It should be pointed out that Theorem 1 in [8] and Corollary 3.2 in [9] are not feasible when employing the LMI Toolbox, but using Theorem 2 in this paper, we can find that system (1) is asymptotically stable. Therefore, our method is less conservative than that in [8, 9].

5. Conclusions

This paper presents some new results of stability analysis for genetic regulatory networks with time-varying delays. An appropriate Lyapunov functional is proposed to investigate the delay-derivative-dependent stability problem. The present results improve the existing ones due to a method to estimate the upper bound of the derivative of Lyapunov functional without ignoring some useful terms and the introduction of convex combination method into the proposed Lyapunov functional, which takes into account the relationship between the time-varying delays and their lower and upper bounds. The supplementary requirements that the time derivatives of time-varying delays must be less than one are removed. As a result, the new stability criterion in terms of LMIs is applicable to both fast and slow time-varying delays. One numerical example shows that the proposed criterion is an improvement over some existing results in the literature. In the future, our work will include the problems of filter design and state estimation for genetic networks.

Conflict of Interests

The authors declare that there is no conflict of interests regarding the publication of this paper.

Acknowledgments

This work is supported by National Natural Science Foundation of China (Grant no. 61103211), Postdoctoral Science Foundation of Chongqing (Grant no. XM201310), and Scientific and Technological Research Program of Chongqing Municipal Education Commission (Grant no. KJ1401403).

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