Predictive analytics of environmental adaptability in multi-omic network models

被引:49
作者
Angione, Claudio [1 ]
Lio, Pietro [1 ]
机构
[1] Univ Cambridge, Comp Lab, Cambridge CB2 1TN, England
关键词
GENE-EXPRESSION; ESCHERICHIA-COLI; CODON USAGE; ADAPTIVE EVOLUTION; PROTEIN ABUNDANCE; MESSENGER-RNA; TRANSLATION; INTEGRATION; FRAMEWORK; DESIGN;
D O I
10.1038/srep15147
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Bacterial phenotypic traits and lifestyles in response to diverse environmental conditions depend on changes in the internal molecular environment. However, predicting bacterial adaptability is still difficult outside of laboratory controlled conditions. Many molecular levels can contribute to the adaptation to a changing environment: pathway structure, codon usage, metabolism. To measure adaptability to changing environmental conditions and over time, we develop a multi-omic model of Escherichia coli that accounts for metabolism, gene expression and codon usage at both transcription and translation levels. After the integration of multiple omics into the model, we propose a multiobjective optimization algorithm to find the allowable and optimal metabolic phenotypes through concurrent maximization or minimization of multiple metabolic markers. In the condition space, we propose Pareto hypervolume and spectral analysis as estimators of short term multi-omic (transcriptomic and metabolic) evolution, thus enabling comparative analysis of metabolic conditions. We therefore compare, evaluate and cluster different experimental conditions, models and bacterial strains according to their metabolic response in a multidimensional objective space, rather than in the original space of microarray data. We finally validate our methods on a phenomics dataset of growth conditions. Our framework, named METRADE, is freely available as a MATLAB toolbox.
引用
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页数:20
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共 80 条
[1]   Global signatures of protein and mRNA expression levels [J].
Abreu, Raquel de Sousa ;
Penalva, Luiz O. ;
Marcotte, Edward M. ;
Vogel, Christine .
MOLECULAR BIOSYSTEMS, 2009, 5 (12) :1512-1526
[2]   Tuning genetic control through promoter engineering [J].
Alper, H ;
Fischer, C ;
Nevoigt, E ;
Stephanopoulos, G .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (36) :12678-12683
[3]   A Hybrid of Metabolic Flux Analysis and Bayesian Factor Modeling for Multiomic Temporal Pathway Activation [J].
Angione, Claudio ;
Pratanwanich, Naruemon ;
Lio, Pietro .
ACS SYNTHETIC BIOLOGY, 2015, 4 (08) :880-889
[4]   Pareto Optimality in Organelle Energy Metabolism Analysis [J].
Angione, Claudio ;
Carapezza, Giovanni ;
Costanza, Jole ;
Lio, Pietro ;
Nicosia, Giuseppe .
IEEE-ACM TRANSACTIONS ON COMPUTATIONAL BIOLOGY AND BIOINFORMATICS, 2013, 10 (04) :1032-1044
[5]   A design automation framework for computational bioenergetics in biological networks [J].
Angione, Claudio ;
Costanza, Jole ;
Carapezza, Giovanni ;
Lio, Pietro ;
Nicosia, Giuseppe .
MOLECULAR BIOSYSTEMS, 2013, 9 (10) :2554-2564
[6]   toyLIFE: a computational framework to study the multi-level organisation of the genotype-phenotype map [J].
Arias, Clemente F. ;
Catalan, Pablo ;
Manrubia, Susanna ;
Cuesta, Jose A. .
SCIENTIFIC REPORTS, 2014, 4
[7]   HypE: An Algorithm for Fast Hypervolume-Based Many-Objective Optimization [J].
Bader, Johannes ;
Zitzler, Eckart .
EVOLUTIONARY COMPUTATION, 2011, 19 (01) :45-76
[8]   SELECTION, MUTATIONS AND CODON USAGE IN A BACTERIAL MODEL [J].
BAGNOLI, F ;
LIO, P .
JOURNAL OF THEORETICAL BIOLOGY, 1995, 173 (03) :271-281
[9]   Context-specific metabolic networks are consistent with experiments [J].
Becker, Scott A. ;
Palsson, Bernhard O. .
PLOS COMPUTATIONAL BIOLOGY, 2008, 4 (05)
[10]   Integration of expression data in genome-scale metabolic network reconstructions [J].
Blazier, Anna S. ;
Papin, Jason A. .
FRONTIERS IN PHYSIOLOGY, 2012, 3