Emergent properties of networks of biological signaling pathways

Science. 1999 Jan 15;283(5400):381-7. doi: 10.1126/science.283.5400.381.

Abstract

Many distinct signaling pathways allow the cell to receive, process, and respond to information. Often, components of different pathways interact, resulting in signaling networks. Biochemical signaling networks were constructed with experimentally obtained constants and analyzed by computational methods to understand their role in complex biological processes. These networks exhibit emergent properties such as integration of signals across multiple time scales, generation of distinct outputs depending on input strength and duration, and self-sustaining feedback loops. Feedback can result in bistable behavior with discrete steady-state activities, well-defined input thresholds for transition between states and prolonged signal output, and signal modulation in response to transient stimuli. These properties of signaling networks raise the possibility that information for "learned behavior" of biological systems may be stored within intracellular biochemical reactions that comprise signaling pathways.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Calcineurin / metabolism
  • Calcium / metabolism
  • Calcium-Calmodulin-Dependent Protein Kinase Type 2
  • Calcium-Calmodulin-Dependent Protein Kinases / metabolism
  • Cell Cycle Proteins*
  • Computer Simulation
  • Cyclic AMP / metabolism
  • Dual Specificity Phosphatase 1
  • Enzyme Activation
  • Epidermal Growth Factor / pharmacology
  • ErbB Receptors / metabolism
  • Feedback
  • Immediate-Early Proteins / metabolism
  • Isoenzymes / metabolism
  • Kinetics
  • Long-Term Potentiation
  • Memory
  • Models, Biological*
  • Neurons / metabolism
  • Phospholipase C gamma
  • Phosphoprotein Phosphatases*
  • Phosphorylation
  • Protein Kinase C / metabolism
  • Protein Phosphatase 1
  • Protein Tyrosine Phosphatases / metabolism
  • Receptors, N-Methyl-D-Aspartate / metabolism
  • Second Messenger Systems
  • Signal Transduction*
  • Synapses / metabolism
  • Type C Phospholipases / metabolism

Substances

  • Cell Cycle Proteins
  • Immediate-Early Proteins
  • Isoenzymes
  • Receptors, N-Methyl-D-Aspartate
  • Epidermal Growth Factor
  • Cyclic AMP
  • ErbB Receptors
  • Protein Kinase C
  • Calcium-Calmodulin-Dependent Protein Kinase Type 2
  • Calcium-Calmodulin-Dependent Protein Kinases
  • Calcineurin
  • Phosphoprotein Phosphatases
  • Protein Phosphatase 1
  • Dual Specificity Phosphatase 1
  • Protein Tyrosine Phosphatases
  • Type C Phospholipases
  • Phospholipase C gamma
  • Calcium