NRC-interacting factor directs neurite outgrowth in an activity-dependent manner

Neuroscience. 2015 Mar 19:289:207-13. doi: 10.1016/j.neuroscience.2014.12.041. Epub 2015 Jan 5.

Abstract

Nuclear hormone receptor coregulator-interacting factor 1 (NIF-1) is a zinc finger nuclear protein that was initially identified to enhance nuclear hormone receptor transcription via its interaction with nuclear hormone receptor coregulator (NRC). NIF-1 may regulate gene transcription either by modulating general transcriptional machinery or remodeling chromatin structure through interactions with specific protein partners. We previously reported that the cytoplasmic/nuclear localization of NIF-1 is regulated by the neuronal Cdk5 activator p35, suggesting potential neuronal functions for NIF-1. The present study reveals that NIF-1 plays critical roles in regulating neuronal morphogenesis at early stages. NIF-1 was prominently expressed in the nuclei of developing rat cortical neurons. Knockdown of NIF-1 expression attenuated both neurite outgrowth in cultured cortical neurons and retinoic acid (RA)-treated Neuro-2a neuroblastoma cells. Furthermore, activity-induced Ca(2+) influx, which is critical for neuronal morphogenesis, stimulated the nuclear localization of NIF-1 in cortical neurons. Suppression of NIF-1 expression reduced the up-regulation of neuronal activity-dependent gene transcription. These findings collectively suggest that NIF-1 directs neuronal morphogenesis during early developmental stages through modulating activity-dependent gene transcription.

Keywords: gene transcription; neuronal development; neuronal morphogenesis; nuclear hormone receptor.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Calcium / metabolism
  • Cell Enlargement
  • Cell Line, Tumor
  • Cell Nucleus / drug effects
  • Cell Nucleus / metabolism
  • Cells, Cultured
  • Central Nervous System Agents / pharmacology
  • Cerebral Cortex / cytology
  • Cerebral Cortex / growth & development
  • Cerebral Cortex / physiology
  • DNA-Binding Proteins
  • Intracellular Signaling Peptides and Proteins / metabolism*
  • Mice
  • Neurites / drug effects
  • Neurites / physiology*
  • Neurogenesis / drug effects
  • Neurogenesis / physiology
  • Nuclear Proteins / metabolism*
  • Rats
  • Transcription Factors
  • Transcription, Genetic / drug effects
  • Transcription, Genetic / physiology
  • Tretinoin / pharmacology

Substances

  • Central Nervous System Agents
  • DNA-Binding Proteins
  • Intracellular Signaling Peptides and Proteins
  • Nuclear Proteins
  • Transcription Factors
  • Zfp335 protein, rat
  • Znf335 protein, mouse
  • Tretinoin
  • Calcium