Differential network biology

被引:555
作者
Ideker, Trey [1 ,2 ,4 ]
Krogan, Nevan J. [3 ,5 ,6 ]
机构
[1] Univ Calif San Diego, Dept Med, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Dept Bioengn, La Jolla, CA 92093 USA
[3] Univ Calif San Francisco, Dept Cellular & Mol Pharmacol, San Francisco, CA 94158 USA
[4] Univ Calif San Diego, Inst Genom Med, La Jolla, CA 92093 USA
[5] Calif Inst Quantitat Biosci, San Francisco, CA USA
[6] J David Gladstone Inst, San Francisco, CA USA
关键词
genetic interactions; networks; protein interactions; PROTEIN-INTERACTION NETWORKS; HIGH-THROUGHPUT; GENETIC INTERACTIONS; GLOBAL ANALYSIS; INTERACTION MAP; BINDING-SITES; MESSENGER-RNA; DNA-DAMAGE; YEAST; REVEALS;
D O I
10.1038/msb.2011.99
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
Protein and genetic interaction maps can reveal the overall physical and functional landscape of a biological system. To date, these interaction maps have typically been generated under a single condition, even though biological systems undergo differential change that is dependent on environment, tissue type, disease state, development or speciation. Several recent interaction mapping studies have demonstrated the power of differential analysis for elucidating fundamental biological responses, revealing that the architecture of an interactome can be massively re-wired during a cellular or adaptive response. Here, we review the technological developments and experimental designs that have enabled differential network mapping at very large scales and highlight biological insight that has been derived from this type of analysis. We argue that differential network mapping, which allows for the interrogation of previously unexplored interaction spaces, will become a standard mode of network analysis in the future, just as differential gene expression and protein phosphorylation studies are already pervasive in genomic and proteomic analysis. Molecular Systems Biology 8: 565; published online 17 January 2012; doi:10.1038/msb.2011.99
引用
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页数:9
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