A local average connectivity-based method for identifying essential proteins from the network level

被引:179
作者
Li, Min [1 ,2 ]
Wang, Jianxin [1 ]
Chen, Xiang [1 ]
Wang, Huan [1 ]
Pan, Yi [1 ,2 ]
机构
[1] Cent S Univ, Sch Informat Sci & Engn, Changsha 410083, Hunan, Peoples R China
[2] Georgia State Univ, Dept Comp Sci, Atlanta, GA 30302 USA
基金
美国国家科学基金会; 中国国家自然科学基金;
关键词
Essential protein; Protein-protein interaction network; Topology; Centrality measure; Local average connectivity; SACCHAROMYCES-CEREVISIAE; ESSENTIAL GENES; COMPLEXES; GENOME; CENTRALITY; IDENTIFICATION; EVOLUTIONARY; PREDICTION; ANNOTATION; TOPOLOGY;
D O I
10.1016/j.compbiolchem.2011.04.002
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Identifying essential proteins is very important for understanding the minimal requirements of cellular survival and development. Fast growth in the amount of available protein-protein interactions has produced unprecedented opportunities for detecting protein essentiality from the network level. Essential proteins have been found to be more abundant among those highly connected proteins. However, there exist a number of highly connected proteins which are not essential. By analyzing these proteins, we find that few of their neighbors interact with each other. Thus, we propose a new local method, named LAC, to determine a protein's essentiality by evaluating the relationship between a protein and its neighbors. The performance of LAC is validated based on the yeast protein interaction networks obtained from two different databases: DIP and BioGRID. The experimental results of the two networks show that the number of essential proteins predicted by LAC clearly exceeds that explored by Degree Centrality (DC). More over, LAC is also compared with other seven measures of protein centrality (Neighborhood Component (DMNC), Betweenness Centrality (BC), Closeness Centrality (CC), Bottle Neck (BN), Information Centrality (IC), Eigenvector Centrality (EC), and Subgraph Centrality (SC)) in identifying essential proteins. The comparison results based on the validations of sensitivity, specificity, F-measure, positive predictive value, negative predictive value, and accuracy consistently show that LAC outweighs these seven previous methods. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:143 / 150
页数:8
相关论文
共 45 条
[1]   Towards the prediction of essential genes by integration of network topology, cellular localization and biological process information [J].
Acencio, Marcio L. ;
Lemke, Ney .
BMC BIOINFORMATICS, 2009, 10 :290
[2]  
[Anonymous], 2009, NUCL ACIDS RES
[3]   Evolutionary and physiological importance of hub proteins [J].
Batada, Nizar N. ;
Hurst, Laurence D. ;
Tyers, Mike .
PLOS COMPUTATIONAL BIOLOGY, 2006, 2 (07) :748-756
[4]   Genome-scale reconstruction of the metabolic network in Staphylococcus aureus N315: an initial draft to the two-dimensional annotation [J].
Becker, SA ;
Palsson, BO .
BMC MICROBIOLOGY, 2005, 5 (1)
[5]  
BONACICH P, 1987, AM J SOCIOL, V92, P1170, DOI 10.1086/228631
[6]   Genome-wide screening for gene function using RNAi in mammalian cells [J].
Cullen, LM ;
Arndt, GM .
IMMUNOLOGY AND CELL BIOLOGY, 2005, 83 (03) :217-223
[7]   Bioinformatics analysis of experimentally determined protein complexes in the yeast Saccharomyces cerevisiae [J].
Dezso, Z ;
Oltvai, ZN ;
Barabási, AL .
GENOME RESEARCH, 2003, 13 (11) :2450-2454
[8]  
ERNESTO E, 2005 VIRTUAL IDENTIF
[9]   Subgraph centrality in complex networks -: art. no. 056103 [J].
Estrada, E ;
Rodríguez-Velázquez, JA .
PHYSICAL REVIEW E, 2005, 71 (05)
[10]   Differences in the evolutionary history of disease genes affected by dominant or recessive mutations [J].
Furney, Simon J. ;
Alba, M. Mar ;
Lopez-Bigas, Nuria .
BMC GENOMICS, 2006, 7 (1)