Zhang Jiabin, Yin Jerry C P, Wesley Cedric S
Neuroscience Training Program, University of Wisconsin-Madison, Madison, WI, 53706, USA.
Cell Mol Neurobiol. 2015 Aug;35(6):763-8. doi: 10.1007/s10571-015-0183-9. Epub 2015 Mar 20.
Notch receptor signaling is evolutionarily conserved and well known for its roles in animal development. Many studies in Drosophila have shown that Notch also performs important functions in memory formation in adult flies. An intriguing observation is that increased expression of the full-length Notch receptor (Nfull) triggers long-term memory (LTM) formation even after very weak training (single training). Canonical Notch signaling is mediated by Notch intracellular domain (NICD), but it is not known whether increased expression of NICD recapitulates the LTM enhancement induced by increased Nfull expression. Here, we report that increased NICD expression either has no impact on LTM formation or suppresses it. Furthermore, it either has no impact or decreases both the levels and activity of cAMP response element binding protein, a key factor supporting LTM. These results indicate that NICD signaling is not sufficient to explain Nfull-induced LTM enhancement. Our findings may also shed light on the molecular mechanisms of memory loss in neurological diseases associated with increased NICD expression and canonical Notch signaling.
Notch受体信号在进化上是保守的,并且因其在动物发育中的作用而广为人知。果蝇中的许多研究表明,Notch在成年果蝇的记忆形成中也发挥着重要作用。一个有趣的观察结果是,即使经过非常微弱的训练(单次训练),全长Notch受体(Nfull)表达的增加也会触发长期记忆(LTM)的形成。经典的Notch信号由Notch细胞内结构域(NICD)介导,但尚不清楚NICD表达的增加是否能重现由Nfull表达增加所诱导的LTM增强。在这里,我们报告NICD表达的增加要么对LTM形成没有影响,要么会抑制它。此外,它要么没有影响,要么会降低环磷酸腺苷反应元件结合蛋白(一种支持LTM的关键因子)的水平和活性。这些结果表明,NICD信号不足以解释Nfull诱导的LTM增强。我们的发现也可能为与NICD表达增加和经典Notch信号相关的神经疾病中记忆丧失的分子机制提供线索。