Chaperones as integrators of cellular networks: Changes of cellular integrity in stress and diseases
arXiv:0710.1622 · doi:10.1002/iub.8
Abstract
Cellular networks undergo rearrangements during stress and diseases. In un-stressed state the yeast protein-protein interaction network (interactome) is highly compact, and the centrally organized modules have a large overlap. During stress several original modules became more separated, and a number of novel modules also appear. A few basic functions, such as the proteasome preserve their central position. However, several functions with high energy demand, such the cell-cycle regulation loose their original centrality during stress. A number of key stress-dependent protein complexes, such as the disaggregation-specific chaperone, Hsp104, gain centrality in the stressed yeast interactome. Molecular chaperones, heat shock, or stress proteins form complex interaction networks (the chaperome) with each other and their partners. Here we show that the human chaperome recovers the segregation of protein synthesis-coupled and stress-related chaperones observed in yeast recently. Examination of yeast and human interactomes shows that (1) chaperones are inter-modular integrators of protein-protein interaction networks, which (2) often bridge hubs and (3) are favorite candidates for extensive phosphorylation. Moreover, chaperones (4) become more central in the organization of the isolated modules of the stressed yeast protein-protein interaction network, which highlights their importance in the de-coupling and re-coupling of network modules during and after stress. Chaperone-mediated evolvability of cellular networks may play a key role in cellular adaptation during stress and various polygenic and chronic diseases, such as cancer, diabetes or neurodegeneration.
arXiv comment13 pages, 3 figures, 1 glossary
References in corpus (13)
- Emergence of scaling in random networks
- Uncovering the overlapping community structure of complex networks in nature and society
- Hierarchical organization of modularity in metabolic networks
- Self-similarity of complex networks
- Detecting rich-club ordering in complex networks
- The efficiency of multi-target drugs: the network approach might help drug design
- Extracting the hierarchical organization of complex systems
- Classes of complex networks defined by role-to-role connectivity profiles
- The rich-club phenomenon across complex network hierarchies
- Some protein interaction data do not exhibit power law statistics
- Stress-induced rearrangements of cellular networks: consequences for protection and drug design
- Propagation of large concentration changes in reversible protein binding networks
- Topological phase transitions of random networks
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- Ageing as a price of cooperation and complexity: Self-organization of complex systems causes the ageing of constituent networks
- Perturbation centrality and Turbine: a novel centrality measure obtained using a versatile network dynamics tool
- System level mechanisms of adaptation, learning, memory formation and evolvability: the role of chaperone and other networks
- Observability transitions in correlated networks
- Network modules help the identification of key transport routes, signaling pathways in cellular and other networks