RC3/neurogranin negatively regulates extracellular signal-regulated kinase pathway through its interaction with Ras

Kanghyun Ryoo, Sang gil Hwang, Kwang Je Kim, Eui Ju Choi

Research output: Contribution to journalArticlepeer-review

2 Citations (Scopus)


RC3/neurogranin is a postsynaptic protein and plays pivotal roles in spatial learning and emotional anxiety as well as synaptic plasticity. The expression level of RC3 is dynamically changed during developmental stages, but the function of RC3 in brain development is not well understood yet. Neurotrophins interact with tropomyosin-related kinase receptors to activate Ras–extracellular signal-regulated kinase (ERK) pathway and can also induce neuronal differentiation. In this study, we demonstrate that RC3 inhibits Ras–ERK pathway by interaction with Ras and controls neurite outgrowth induced by neurotrophins. In PC12 cells, RC3 inhibits nerve growth factor (NGF)-induced activation of Ras and thereby ERK1/2 signaling cascade as well as neurite outgrowth induced by NGF. We found Ras is the target of the inhibitory function of RC3, because RC3 interacts with Ras and suppresses the elevated affinity of Ras to Ras-binding domain of Raf-1. Meanwhile, already activated Raf-1 by Ras activity is not affected by RC3. Furthermore, depletion of RC3 by RNA interference drastically enhances the stimulation of ERK1/2 and neurite outgrowth induced by brain-derived neurotrophic factor in hippocampal neurons. These findings suggest that RC3 is a novel natural inhibitor of Ras-ERK1/2 signaling axis, leading to negatively regulate neuronal differentiation induced by neurotrophins.

Original languageEnglish
Pages (from-to)33-40
Number of pages8
JournalMolecular and Cellular Biochemistry
Issue number1-2
Publication statusPublished - 2014 Apr

Bibliographical note

Publisher Copyright:
© 2014, Springer Science+Business Media New York.


  • ERK1/2
  • Neurite outgrowth
  • Neurotrophin
  • RC3
  • Ras

ASJC Scopus subject areas

  • Molecular Biology
  • Clinical Biochemistry
  • Cell Biology


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