TY - JOUR
T1 - Physical Module Networks
T2 - An integrative approach for reconstructing transcription regulation
AU - Novershtern, Noa
AU - Regev, Aviv
AU - Friedman, Nir
N1 - Funding Information:
Funding: US-Israel Binational Foundation (BSF) grant (to N.F. and A.R., in part).
PY - 2011/7
Y1 - 2011/7
N2 - Motivation: Deciphering the complex mechanisms by which regulatory networks control gene expression remains a major challenge. While some studies infer regulation from dependencies between the expression levels of putative regulators and their targets, others focus on measured physical interactions. Results: Here, we present Physical Module Networks, a unified framework that combines a Bayesian model describing modules of co-expressed genes and their shared regulation programs, and a physical interaction graph, describing the protein-protein interactions and protein-DNA binding events that coherently underlie this regulation. Using synthetic data, we demonstrate that a Physical Module Network model has similar recall and improved precision compared to a simple Module Network, as it omits many false positive regulators. Finally, we show the power of Physical Module Networks to reconstruct meaningful regulatory pathways in the genetically perturbed yeast and during the yeast cell cycle, as well as during the response of primary epithelial human cells to infection with H1N1 influenza.
AB - Motivation: Deciphering the complex mechanisms by which regulatory networks control gene expression remains a major challenge. While some studies infer regulation from dependencies between the expression levels of putative regulators and their targets, others focus on measured physical interactions. Results: Here, we present Physical Module Networks, a unified framework that combines a Bayesian model describing modules of co-expressed genes and their shared regulation programs, and a physical interaction graph, describing the protein-protein interactions and protein-DNA binding events that coherently underlie this regulation. Using synthetic data, we demonstrate that a Physical Module Network model has similar recall and improved precision compared to a simple Module Network, as it omits many false positive regulators. Finally, we show the power of Physical Module Networks to reconstruct meaningful regulatory pathways in the genetically perturbed yeast and during the yeast cell cycle, as well as during the response of primary epithelial human cells to infection with H1N1 influenza.
UR - http://www.scopus.com/inward/record.url?scp=79959454002&partnerID=8YFLogxK
U2 - 10.1093/bioinformatics/btr222
DO - 10.1093/bioinformatics/btr222
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C2 - 21685068
AN - SCOPUS:79959454002
SN - 1367-4803
VL - 27
SP - i177-i185
JO - Bioinformatics
JF - Bioinformatics
IS - 13
M1 - btr222
ER -