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Updated: Jun 26, 2026

Inducing Cre-lox Recombination in Mouse Cerebral Cortex Through In Utero Electroporation
Published on: November 17, 2017
The CREB/CREM transcription factors negatively regulate early synaptogenesis and spontaneous network activity
Fernando Aguado1, Carmen Díaz-Ruiz, Rosanna Parlato
1Department of Cell Biology, Centro de Investigación Biomédica en Red para Enfermedades Neurodegenerativas, Institute for Research in Biomedicine, University of Barcelona, Barcelona, Spain.
Abstract:
The family of CREB (cAMP response element-binding protein) transcription factors are involved in a variety of biological processes including the development and plasticity of the nervous system. In the maturing and adult brain, CREB genes are required for activity-dependent processes, including synaptogenesis, refinement of connections and long-term potentiation. Here, we use CREB1(Nescre)CREM(-/-) (cAMP-responsive element modulator) mutants to investigate the role of these genes in stimulus-independent patterns of neural activity at early stages. We show that lack of CREB/CREM genes specifically in neural tissue leads to increased synaptogenesis and to a dramatic increase in the levels of spontaneous network activity at embryonic stages. Thus, the functions of CREB/CREM genes in neural activity differ in distinct periods of neural development.
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