| | | | | Table of ContentsReports Articles Reports | Volume 11, Number 4 | Reports | When cultured in medium containing two carbon substrates, E. coli frequently consumes both simultaneously. A mathematical formula based on simple assumptions accurately predicts the resulting growth rate from the growth rate on each substrate alone. Rutger Hermsen, Hiroyuki Okano, Conghui You, Nicole Werner, and Terence Hwa | Articles | A systems biology approach integrating genome‐wide genetic variation and transcriptome profiling data from participants of the Framingham Heart Study identifies key regulatory genes and gene networks underlying blood pressure control. Tianxiao Huan, Qingying Meng, Mohamed A Saleh, Allison E Norlander, Roby Joehanes, Jun Zhu, Brian H Chen, Bin Zhang, Andrew D Johnson, Saixia Ying, Paul Courchesne, Nalini Raghavachari, Richard Wang, Poching Liu, The International Consortium for Blood Pressure GWAS (ICBP), Christopher J O'Donnell, Ramachandran Vasan, Peter J Munson, Meena S Madhur, David G Harrison, Xia Yang, and Daniel Levy | | A differential genetic interaction screen performed in different stress conditions shows that genetic interactions are often context specific. Conditional genetic interactions recapitulate known signalling interactions and can be used to identify novel conditional functional associations. Humberto Martin, Michael Shales, Pablo Fernandez‐Piñar, Ping Wei, Maria Molina, Dorothea Fiedler, Kevan M Shokat, Pedro Beltrao, Wendell Lim, and Nevan J Krogan | | Dynamic experiments and a computational method are co‐designed to infer causal interactions between metabolism, signaling and transcription. Model‐based data integration suggests new candidates for inputs and targets of yeast nitrogen signaling via TOR complex 1. Ana Paula Oliveira, Sotiris Dimopoulos, Alberto Giovanni Busetto, Stefan Christen, Reinhard Dechant, Laura Falter, Morteza Haghir Chehreghani, Szymon Jozefczuk, Christina Ludwig, Florian Rudroff, Juliane Caroline Schulz, Asier González, Alexandre Soulard, Daniele Stracka, Ruedi Aebersold, Joachim M Buhmann, Michael N Hall, Matthias Peter, Uwe Sauer, and Jörg Stelling | | A new strategy, involving optical shaping of gradients, allows systematically analyzing components regulating cell migration speed and directionality. The approach is applied to characterize migration and chemotaxis phenotypes for 285 siRNA perturbations in human neutrophils. Sean R Collins, Hee Won Yang, Kimberly M Bonger, Emmanuel G Guignet, Thomas J Wandless, and Tobias Meyer | Reports | A general principle of bacterial growth enables the prediction of mutant growth rates under drug combinations. Rare violations of this principle expose cellular functions that control drug interactions and can be targeted by small molecules to alter drug interactions in predictable ways. Guillaume Chevereau and Tobias Bollenbach | | | |
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