4.3 Article

Regulation of cpg15 by signaling pathways that mediate synaptic plasticity

Journal

MOLECULAR AND CELLULAR NEUROSCIENCE
Volume 24, Issue 3, Pages 538-554

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/S1044-7431(03)00230-6

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Funding

  1. NATIONAL EYE INSTITUTE [R01EY011894] Funding Source: NIH RePORTER
  2. NEI NIH HHS [R01 EY011894, R01 EY011894-07A2] Funding Source: Medline

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Transcriptional activation is a key link between neuronal activity and long-term synaptic plasticity. Little is known about genes responding to this activation whose products directly effect functional and structural changes at the synapse. cpg15 is an activity-regulated gene encoding a membrane-bound ligand that regulates dendritic and axonal arbor growth and synaptic maturation. We report that cpg15 is an immediate-early gene induced by Ca2+ influx through NMDA receptors and L-type voltage-sensitive calcium channels. Activity-dependent cpg15 expression requires convergent activation of the CaM kinase and MAP kinase pathways. Although activation of PKA is not required for activity-dependent expression, cpg15 is induced by CAMP in active neurons. CREB binds the cpg15 promoter in vivo and partially regulates its activity-dependent expression. cpg15 is an effector gene that is a target for signal transduction pathways that mediate synaptic plasticity and thus may take part in an activity-regulated transcriptional program that directs long-term changes in synaptic connections. (C) 2003 Elsevier Inc. All rights reserved.

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