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DARPP-32 is a robust integrator of dopamine and glutamate signals
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- EMBL–EBI, Wellcome-Trust Genome Campus, Hinxton, United Kingdom
- INSERM U536, Institut du Fer a Moulin, Paris, France
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- Document Type:
- Poster
- Date:
- Received 30 November 2006 13:14 UTC; Posted 30 November 2006
- Subjects:
- Neuroscience
- Abstract:
Integration of neurotransmitter and neuromodulator signals in the striatum plays a central role in the functions and dysfunctions of the basal ganglia. DARPP-32 is a key actor of this integration in the GABAergic medium-size spiny neurons, in particular in response to dopamine and glutamate. When phosphorylated by cAMP-dependent protein kinase (PKA) DARPP-32 inhibits protein phosphatase-1 (PP1), whereas when phosphorylated by cyclin-dependent kinase 5 (CDK5) it inhibits PKA. DARPP-32 is also regulated by casein kinases and by several protein phosphatases. These complex and intricate regulations make simple predictions of DARPP-32 dynamic behaviour virtually impossible. We used detailed quantitative modelling of the regulation of DARPP-32 phosphorylation to improve our understanding of its function. The models included all the combinations of the three best characterized phosphorylation sites of DARPP-32, their regulation by kinases and phosphatases, and the regulation of those enzymes by cAMP and Ca2+ signals. Dynamic simulations allowed to observe the temporal relationships between cAMP and Ca2+ signals. We confirmed that the proposed regulation of protein phosphatase-2A (PP2A) by calcium can account for the observed decrease of Threonine 75 phosphorylation upon glutamate receptor activation. Sensitivity analysis showed that CDK5 activity is a major regulator of the response, as previously suggested. Conversely, the regulation of PP2A by PKA or by calcium, had little effect on the function of DARPP-32 in these conditions. The simulations showed that DARPP-32 is not only a robust signal integrator, but also a coincidence detector, the delay between cAMP and calcium signals affecting the response to the latter. This integration did not depend on the concentration of DARPP-32, while the absolute response on PP1 varied linearly. In silico mutants showed that Ser137 phosphorylation affects the coincidence detector function, and that constitutive phosphorylation in Ser137 transforms DARPP-32 in a quasi-irreversible switch. This work is a first attempt to better understand the complex interactions between cAMP and Ca2+ regulation of DARPP-32. Progressive inclusion of additional components should lead to a realistic model of signalling networks underlying the function of striatal neurons.
- Presented at:
- 7th International Conference on Systems Biology, 09 October 2006
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- This document is licensed to the public under the Creative Commons Attribution 2.5 License
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Le Novere, Nicolas, Fernandez, Eric, Schiappa, Renaud, and Girault, Jean-Antoine. DARPP-32 is a robust integrator of dopamine and glutamate signals. Available from Nature Precedings <http://dx.doi.org/10.1038/npre.2006.9.1> (2006)
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- 10.1371/journal.pcbi.0020176.eor (Peer Reviewed):