A Novel Knowledge-Driven Systems Biology Approach for Phenotype Prediction upon Genetic Intervention

被引:33
作者
Chang, Rui [1 ]
Shoemaker, Robert [1 ]
Wang, Wei [1 ]
机构
[1] UCSD, Dept Chem & Biochem, La Jolla, CA 92093 USA
关键词
Dynamic Bayesian network; genetic network; phenotype prediction; genetic intervention; systems biology; breast cancer; cell proliferation; BREAST-CANCER CELLS; GROWTH-FACTOR-BETA; TGF-BETA; REGULATORY NETWORKS; TRANSCRIPTIONAL NETWORK; EXPRESSION DATA; CYCLE ARREST; C-MYC; RECONSTRUCTION; REPRESSION;
D O I
10.1109/TCBB.2011.18
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Deciphering the biological networks underlying complex phenotypic traits, e. g., human disease is undoubtedly crucial to understand the underlying molecular mechanisms and to develop effective therapeutics. Due to the network complexity and the relatively small number of available experiments, data-driven modeling is a great challenge for deducing the functions of genes/proteins in the network and in phenotype formation. We propose a novel knowledge-driven systems biology method that utilizes qualitative knowledge to construct a Dynamic Bayesian network (DBN) to represent the biological network underlying a specific phenotype. Edges in this network depict physical interactions between genes and/or proteins. A qualitative knowledge model first translates typical molecular interactions into constraints when resolving the DBN structure and parameters. Therefore, the uncertainty of the network is restricted to a subset of models which are consistent with the qualitative knowledge. All models satisfying the constraints are considered as candidates for the underlying network. These consistent models are used to perform quantitative inference. By in silico inference, we can predict phenotypic traits upon genetic interventions and perturbing in the network. We applied our method to analyze the puzzling mechanism of breast cancer cell proliferation network and we accurately predicted cancer cell growth rate upon manipulating (anti) cancerous marker genes/proteins.
引用
收藏
页码:1170 / 1182
页数:13
相关论文
共 52 条
[31]   Pathway analysis in metabolic databases via differential metabolic display (DMD) [J].
Küffner, R ;
Zimmer, R ;
Lengauer, T .
BIOINFORMATICS, 2000, 16 (09) :825-836
[32]  
LAURITZEN SL, 1988, J ROY STAT SOC B MET, V50, P157
[33]   The yeast cell-cycle network is robustly designed [J].
Li, FT ;
Long, T ;
Lu, Y ;
Ouyang, Q ;
Tang, C .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (14) :4781-4786
[34]   ARACNE: An algorithm for the reconstruction of gene regulatory networks in a mammalian cellular context [J].
Margolin, AA ;
Nemenman, I ;
Basso, K ;
Wiggins, C ;
Stolovitzky, G ;
Dalla Favera, R ;
Califano, A .
BMC BIOINFORMATICS, 2006, 7 (Suppl 1)
[35]  
Murphy K. P., 2002, Dynamic bayesian networks: representation, inference and learning
[36]   Connecting quantitative regulatory-network models to the genome [J].
Pan, Yue ;
Durfee, Tim ;
Bockhorst, Joseph ;
Craven, Mark .
BIOINFORMATICS, 2007, 23 (13) :I367-I376
[37]  
Pearl J., 1988, PROBABILISTIC REASON, DOI DOI 10.1016/C2009-0-27609-4
[38]  
POLYAK K, 1994, CELL
[39]   Qualitative analysis of biochemical reaction systems [J].
Reddy, VN ;
Liebman, MN ;
Mavrovouniotis, ML .
COMPUTERS IN BIOLOGY AND MEDICINE, 1996, 26 (01) :9-24
[40]   KIP/CIP AND INK4 CDK INHIBITORS COOPERATE TO INDUCE CELL-CYCLE ARREST IN RESPONSE TO TGF-BETA [J].
REYNISDOTTIR, I ;
POLYAK, K ;
IAVARONE, A ;
MASSAGUE, J .
GENES & DEVELOPMENT, 1995, 9 (15) :1831-1845