Deterministic Effects Propagation Networks for reconstructing protein signaling networks from multiple interventions

被引:17
作者
Froehlich, Holger [1 ]
Sahin, Oezguer [1 ]
Arlt, Dorit [1 ]
Bender, Christian [1 ]
Beissbarth, Tim [1 ,2 ]
机构
[1] German Canc Res Ctr, D-69120 Heidelberg, Germany
[2] Univ Med Gottingen, D-37099 Gottingen, Germany
关键词
GENE-EXPRESSION; MODELS; PERTURBATIONS; TRASTUZUMAB; ACTIVATION; ARRAY;
D O I
10.1186/1471-2105-10-322
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Background: Modern gene perturbation techniques, like RNA interference (RNAi), enable us to study effects of targeted interventions in cells efficiently. In combination with mRNA or protein expression data this allows to gain insights into the behavior of complex biological systems. Results: In this paper, we propose Deterministic Effects Propagation Networks (DEPNs) as a special Bayesian Network approach to reverse engineer signaling networks from a combination of protein expression and perturbation data. DEPNs allow to reconstruct protein networks based on combinatorial intervention effects, which are monitored via changes of the protein expression or activation over one or a few time points. Our implementation of DEPNs allows for latent network nodes (i.e. proteins without measurements) and has a built in mechanism to impute missing data. The robustness of our approach was tested on simulated data. We applied DEPNs to reconstruct the ERBB signaling network in de novo trastuzumab resistant human breast cancer cells, where protein expression was monitored on Reverse Phase Protein Arrays (RPPAs) after knockdown of network proteins using RNAi. Conclusion: DEPNs offer a robust, efficient and simple approach to infer protein signaling networks from multiple interventions. The method as well as the data have been made part of the latest version of the R package "nem" available as a supplement to this paper and via the Bioconductor repository.
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页数:16
相关论文
共 44 条
[1]  
Aho A. V., 1972, SIAM Journal on Computing, V1, P131, DOI 10.1137/0201008
[2]   The ErbB signaling network in embryogenesis and oncogenesis: Signal diversification through combinatorial ligand-receptor interactions [J].
Alroy, I ;
Yarden, Y .
FEBS LETTERS, 1997, 410 (01) :83-86
[3]   Modeling the temporal interplay of molecular signaling and gene expression by using dynamic nested effects models [J].
Anchang, Benedict ;
Sadeh, Mohammad J. ;
Jacob, Juby ;
Tresch, Achim ;
Vlad, Marcel O. ;
Oefner, Peter J. ;
Spang, Rainer .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2009, 106 (16) :6447-6452
[4]   A comparison of normalization methods for high density oligonucleotide array data based on variance and bias [J].
Bolstad, BM ;
Irizarry, RA ;
Åstrand, M ;
Speed, TP .
BIOINFORMATICS, 2003, 19 (02) :185-193
[5]   Lineage specific composition of cyclin D-CDK4/CDK6-p27 complexes reveals distinct functions of CDK4, CDK6 and individual D-type cyclins in differentiating cells of embryonic origin [J].
Bryja, V. ;
Pachernik, J. ;
Vondracek, J. ;
Soucek, K. ;
Cajanek, L. ;
Horvath, V. ;
Holubcova, Z. ;
Dvorak, P. ;
Hampl, A. .
CELL PROLIFERATION, 2008, 41 (06) :875-893
[6]  
Cowell RG., 2007, Probabilistic Networks and Expert Systems: Exact Computational Methods for Bayesian Networks
[7]  
Davison A. C., 1997, Bootstrap methods and their application, DOI 10.1017/CBO9780511802843
[8]   MAXIMUM LIKELIHOOD FROM INCOMPLETE DATA VIA EM ALGORITHM [J].
DEMPSTER, AP ;
LAIRD, NM ;
RUBIN, DB .
JOURNAL OF THE ROYAL STATISTICAL SOCIETY SERIES B-METHODOLOGICAL, 1977, 39 (01) :1-38
[9]   Applying dynamic Bayesian networks to perturbed gene expression data [J].
Dojer, Norbert ;
Gambin, Anna ;
Mizera, Andrzej ;
Wilczynski, Bartek ;
Tiuryn, Jerzy .
BMC BIOINFORMATICS, 2006, 7 (1)
[10]   Potent and specific genetic interference by double-stranded RNA in Caenorhabditis elegans [J].
Fire, A ;
Xu, SQ ;
Montgomery, MK ;
Kostas, SA ;
Driver, SE ;
Mello, CC .
NATURE, 1998, 391 (6669) :806-811