Abstract
Members of the cyclic-AMP response-element binding protein (CREB) transcription factor family regulate the expression of genes needed for long-term memory formation. Loss of Notch impairs long-term, but not short-term, memory in flies and mammals. We investigated if the Notch-1 (N1) exerts an effect on CREB-dependent gene transcription. We observed that N1 inhibits CREB mediated activation of cyclic-AMP response element (CRE) containing promoters in a γ-secretase-dependent manner. We went on to find that the γ-cleaved N1 intracellular domain (N1ICD) sequesters nuclear CREB1α, inhibits cAMP/PKA-mediated neurite outgrowth and represses the expression of specific CREB regulated genes associated with learning and memory in primary cortical neurons. Similar transcriptional effects were observed with the N2ICD, N3ICD and N4ICDs. Together, these observations indicate that the effects of Notch on learning and memory are, at least in part, via an effect on CREB-regulated gene expression.
| Original language | English |
|---|---|
| Pages (from-to) | 621-629 |
| Number of pages | 9 |
| Journal | Cellular Signalling |
| Volume | 27 |
| Issue number | 3 |
| DOIs | |
| State | Published - Mar 1 2015 |
ASJC Scopus Subject Areas
- Cell Biology
Keywords
- Alzheimer's disease
- CREB
- Memory
- NICD
- PKA
- Protein Isoforms/chemistry
- Cyclic AMP-Dependent Protein Kinases/metabolism
- Cyclic AMP/pharmacology
- Humans
- Receptor, Notch1/chemistry
- Memory, Long-Term/physiology
- Colforsin/pharmacology
- HEK293 Cells
- Female
- Transcription, Genetic/drug effects
- Protein Structure, Tertiary
- Neurites/physiology
- Mice, Inbred C57BL
- Cells, Cultured
- Rats
- Neurons/cytology
- Cyclic AMP Response Element-Binding Protein/genetics
- Amyloid Precursor Protein Secretases/metabolism
- Animals
- Embryo, Mammalian/cytology
- Mice
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