Functional modules by relating protein interaction networks and gene expression

被引:124
作者
Tornow, S
Mewes, HW
机构
[1] German Natl Ctr Hlth & environm, Inst Bioinformat, D-85764 Neuherberg, Germany
[2] Tech Univ Munich, Wissensch Zentrum Weihenstephan, Lehrstuhl Genomorientierte Bioinformat, D-85435 Freising Weihenstephan, Germany
关键词
D O I
10.1093/nar/gkg838
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Genes and proteins are organized on the basis of their particular mutual relations or according to their interactions in cellular and genetic networks. These include metabolic or signaling pathways and protein interaction, regulatory or co-expression networks. Integrating the information from the different types of networks may lead to the notion of a functional network and functional modules. To find these modules, we propose a new technique which is based on collective, multi-body correlations in a genetic network. We calculated the correlation strength of a group of genes (e.g. in the co-expression network) which were identified as members of a module in a different network (e.g. in the protein interaction network) and estimated the probability that this correlation strength was found by chance. Groups of genes with a significant correlation strength in different networks have a high probability that they perform the same function. Here, we propose evaluating the multi-body correlations by applying the superparamagnetic approach. We compare our method to the presently applied mean Pearson correlations and show that our method is more sensitive in revealing functional relationships.
引用
收藏
页码:6283 / 6289
页数:7
相关论文
共 32 条
[1]   Extreme self-organization in networks constructed from gene expression data [J].
Agrawal, H .
PHYSICAL REVIEW LETTERS, 2002, 89 (26)
[2]   Potts ferromagnets on coexpressed gene networks: Identifying maximally stable partitions [J].
Agrawal, H ;
Domany, E .
PHYSICAL REVIEW LETTERS, 2003, 90 (15) :4
[3]   Emergence of scaling in random networks [J].
Barabási, AL ;
Albert, R .
SCIENCE, 1999, 286 (5439) :509-512
[4]   Superparamagnetic clustering of data [J].
Blatt, M ;
Wiseman, S ;
Domany, E .
PHYSICAL REVIEW LETTERS, 1996, 76 (18) :3251-3254
[5]   A genome-wide transcriptional analysis of the mitotic cell cycle [J].
Cho, RJ ;
Campbell, MJ ;
Winzeler, EA ;
Steinmetz, L ;
Conway, A ;
Wodicka, L ;
Wolfsberg, TG ;
Gabrielian, AE ;
Landsman, D ;
Lockhart, DJ ;
Davis, RW .
MOLECULAR CELL, 1998, 2 (01) :65-73
[7]  
Fellenberg M, 2000, Proc Int Conf Intell Syst Mol Biol, V8, P152
[8]   Functional organization of the yeast proteome by systematic analysis of protein complexes [J].
Gavin, AC ;
Bösche, M ;
Krause, R ;
Grandi, P ;
Marzioch, M ;
Bauer, A ;
Schultz, J ;
Rick, JM ;
Michon, AM ;
Cruciat, CM ;
Remor, M ;
Höfert, C ;
Schelder, M ;
Brajenovic, M ;
Ruffner, H ;
Merino, A ;
Klein, K ;
Hudak, M ;
Dickson, D ;
Rudi, T ;
Gnau, V ;
Bauch, A ;
Bastuck, S ;
Huhse, B ;
Leutwein, C ;
Heurtier, MA ;
Copley, RR ;
Edelmann, A ;
Querfurth, E ;
Rybin, V ;
Drewes, G ;
Raida, M ;
Bouwmeester, T ;
Bork, P ;
Seraphin, B ;
Kuster, B ;
Neubauer, G ;
Superti-Furga, G .
NATURE, 2002, 415 (6868) :141-147
[9]   Correlation between transcriptome and interactome mapping data from Saccharomyces cerevisiae [J].
Ge, H ;
Liu, ZH ;
Church, GM ;
Vidal, M .
NATURE GENETICS, 2001, 29 (04) :482-486
[10]   Coupled two-way clustering analysis of gene microarray data [J].
Getz, G ;
Levine, E ;
Domany, E .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (22) :12079-12084