4.6 Article

The Notch intracellular domain represses CRE-dependent transcription

Journal

CELLULAR SIGNALLING
Volume 27, Issue 3, Pages 621-629

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.cellsig.2014.11.034

Keywords

CREB; NICD; PKA; Alzheimer's disease; Memory

Categories

Funding

  1. Alzheimer's Research UK [001214]
  2. Wellcome Trust [00117]
  3. Alzheimers Research UK [ART-PhD2005-2] Funding Source: researchfish
  4. National Institute for Health Research [NF-SI-0512-10053] Funding Source: researchfish

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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 gamma-secretase-dependent manner. We went on to find that the gamma-cleaved N1 intracellular domain (N1ICD) sequesters nuclear CREB1 alpha, 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. (C) 2014 The Authors. Published by Elsevier Inc This is an open access article under the CC BY-NC-ND license.

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