Abstract
A wide range of growth factors encode information into specific temporal patterns of MAP kinase (MAPK) and CREB phosphorylation, which are further decoded by expression of immediate early gene products (IEGs) to exert biological functions. However, the IEG decoding system remain unknown. We built a data-driven based on time courses of MAPK and CREB phosphorylation and IEG expression in response to various growth factors to identify how signal is processed. We found that IEG expression uses common decoding systems regardless of growth factors and expression of each IEG differs in upstream dependency, switch-like response, and linear temporal filters. Pulsatile ERK phosphorylation was selectively decoded by expression of EGR1 rather than c-FOS. Conjunctive NGF and PACAP stimulation was selectively decoded by synergistic JUNB expression through switch-like response to c-FOS. Thus, specific temporal patterns and combinations of MAPKs and CREB phosphorylation can be decoded by selective IEG expression via distinct temporal filters and switch-like responses. The data-driven modeling is versatile for analysis of signal processing and does not require detailed prior knowledge of pathways.
Publication types
-
Research Support, Non-U.S. Gov't
MeSH terms
-
Animals
-
Anisomycin / pharmacology
-
Cyclic AMP Response Element-Binding Protein / genetics*
-
Cyclic AMP Response Element-Binding Protein / metabolism
-
Gene Expression Regulation / drug effects
-
Genes, Immediate-Early*
-
Mitogen-Activated Protein Kinases / genetics*
-
Mitogen-Activated Protein Kinases / metabolism
-
Models, Biological*
-
Nerve Growth Factor / pharmacology
-
PC12 Cells / cytology
-
PC12 Cells / drug effects
-
PC12 Cells / metabolism*
-
Phosphorylation / drug effects
-
Pituitary Adenylate Cyclase-Activating Polypeptide / pharmacology
-
Proto-Oncogene Proteins c-fos / genetics
-
Proto-Oncogene Proteins c-fos / metabolism
-
Rats
-
Signal Transduction / drug effects
-
Time Factors
-
Transcription Factors / genetics
-
Transcription Factors / metabolism
Substances
-
Cyclic AMP Response Element-Binding Protein
-
Pituitary Adenylate Cyclase-Activating Polypeptide
-
Proto-Oncogene Proteins c-fos
-
Transcription Factors
-
Anisomycin
-
Nerve Growth Factor
-
Mitogen-Activated Protein Kinases
Grants and funding
This work was supported by The Dynamic Mechanisms of and Fundamental Technology for Biological Systems, and the Creation of Fundamental Technologies for Understanding and Control of Biosystem Dynamics, CREST, from the Japan Science and Technology (JST); by a KAKENHI Scientific Research grant (A) (#21240025) from the Ministry of Education, Culture, Sports, Science and Technology of Japan (MEXT); by the Strategic International Cooperative Program (Research Exchange Type), JST, and by a Human Frontier Science Project (HFSP) grant (RGP0061/2011). T.H.S. is a research fellow of the Japan Society for the Promotion of Science (JSPS). The funders had no role in study design, data collection and analysis, decision to publish, or prepartion of the manuscript.